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		<title>TRIOSEPHOSPHATE ISOMERASE (TPI) A DIMERIC GLYCOLYTIC ENZYME AS A MODEL OF TIM-BARREL ACTIVE-SITE STRUCTURAL AND CHEMICAL ASPECTS IN THE MONOMER LOOP REGION&#8217;S REVERSIBLE CATALYTIC REACTION.</title>
		<link>https://faroucheombre.wordpress.com/2016/04/10/triosephosphate-isomerase-tpi-a-dimeric-glycolytic-enzyme-as-a-model-of-tim-barrel-active-site-structural-and-chemical-aspects-in-the-monomer-loop-regions-reversible-catalytic-reaction/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sun, 10 Apr 2016 17:46:46 +0000</pubDate>
				<category><![CDATA[DHAP]]></category>
		<category><![CDATA[g3p]]></category>
		<category><![CDATA[methylglyoxal]]></category>
		<category><![CDATA[tpi]]></category>
		<category><![CDATA[Triosephosphate isomerase]]></category>
		<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[NADPH]]></category>
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					<description><![CDATA[Triosephosphate isomerase (TPI, EC 5.3.1.1) is essential to glycolysis, catalyzes the fifth step in the glycolysis pathway the reversible conversion of dihydroxyacetone phosphate (DHAP) into glyceraldehyde-3-phosphate. TPI is a homodimer formed by two identical dimeric molecules of a single structural locus : 12p13.31. TPI has only 1 functional gene with a molecular mass of 29 [&#8230;]]]></description>
		
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			<media:title type="html">dhap-g3p</media:title>
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		<title>Non-Phosphorylating And Phosphorylating Oxidoreductase Glyceraldehyde-3-Phosphate Dehydrogenase As Part Of A Structure-Based Design In Glycolysis As The Glycolytic Protein G3PD.</title>
		<link>https://faroucheombre.wordpress.com/2015/11/20/non-phosphorylating-and-phosphorylating-oxidoreductase-glyceraldehyde-3-phosphate-dehydrogenase-as-part-of-a-structure-based-design-in-glycolysis-as-the-glycolytic-protein-g3pd/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Fri, 20 Nov 2015 17:30:49 +0000</pubDate>
				<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[1 2 3-bpg]]></category>
		<category><![CDATA[3pg]]></category>
		<category><![CDATA[atp]]></category>
		<category><![CDATA[cgp-3466]]></category>
		<category><![CDATA[embden-meyerhof]]></category>
		<category><![CDATA[g3p]]></category>
		<category><![CDATA[gait]]></category>
		<category><![CDATA[gapc]]></category>
		<category><![CDATA[GAPDH]]></category>
		<category><![CDATA[nad]]></category>
		<category><![CDATA[NADPH]]></category>
		<category><![CDATA[pgk]]></category>
		<category><![CDATA[rp-l13]]></category>
		<category><![CDATA[s-nitrosylation]]></category>
		<category><![CDATA[siah1]]></category>
		<category><![CDATA[tpi]]></category>
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					<description><![CDATA[Glyceraldehyde-3-phosphate dehydrogenase (EC 1.2.1.12) GAPDH1/G3PD, is located in band 12p13.31; related to both glycolysis2 and gluconeogenesis-pathways. G3PD catalyzes reversible oxidative phosphorylation of inorganic phosphate and nicotinamide3 adenine dinucleotide (NAD)4 converting in glycolysis the glycolytic protein GAPDH5 in which adenosine-triphosphate (ATP)6 is generated when phosphoglycerate kinase (PGK)7 is produced in the GAPDH8-catalyzed reaction. These intermediate metabolites [&#8230;]]]></description>
		
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			<media:title type="html">g3p</media:title>
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		<item>
		<title>CHANGES IN GLUTATHIONE AND GLUTATHIONE REDUCTASE POSITIONING GLUTATHIONE-S-TRANSFERASE AS A FUNCTION OF CELL CONCENTRATION WITH ENZYME ACTIVITIES FOUND TO INFLUENCE BEHAVIOR.</title>
		<link>https://faroucheombre.wordpress.com/2015/06/14/changes-in-glutathione-and-glutathione-reductase-positioning-glutathione-s-transferase-as-a-function-of-cell-concentration-with-enzyme-activities-found-to-influence-behavior/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sun, 14 Jun 2015 18:30:15 +0000</pubDate>
				<category><![CDATA[GSH glutathione]]></category>
		<category><![CDATA[catalase]]></category>
		<category><![CDATA[FAD]]></category>
		<category><![CDATA[G6PD]]></category>
		<category><![CDATA[glutathione-GSH]]></category>
		<category><![CDATA[Glutathione-Reductase_GSR]]></category>
		<category><![CDATA[GRX-glutatredoxin]]></category>
		<category><![CDATA[NADPH]]></category>
		<category><![CDATA[riboflavin]]></category>
		<category><![CDATA[thioltransferase-TTase]]></category>
		<category><![CDATA[TRX]]></category>
		<category><![CDATA[TRXR]]></category>
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					<description><![CDATA[Glutathione reductase (GSR, GR) locus in the chromosomal region 8p21.1, (EC 1.8.1.7)-(§, ‡) is a protein-S-glutathionylation, as a (human) Mitochondrial localization of hGSR and its associated enzymes cellular thiol/disulfides S-Glutathione reductase (GSR) which is the importance of significance in reversible thiol modifications which  regenerates reduced glutathione (GSH) and GSSG to the reduced form found in [&#8230;]]]></description>
		
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			<media:title type="html">PDB Id: 3DK9</media:title>
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			<media:title type="html">Glutathione reductase</media:title>
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		<title>Thioredoxin reductase: Selenotetrapeptide sequences with specificity for thioredoxin and glutathione systems</title>
		<link>https://faroucheombre.wordpress.com/2015/03/01/thioredoxin-reductase-selenotetrapeptide-sequences-with-specificity-for-thioredoxin-and-glutathione-systems/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sun, 01 Mar 2015 19:17:15 +0000</pubDate>
				<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[catalase]]></category>
		<category><![CDATA[FAD]]></category>
		<category><![CDATA[glutaredoxin]]></category>
		<category><![CDATA[glutathione]]></category>
		<category><![CDATA[GRX]]></category>
		<category><![CDATA[GSH]]></category>
		<category><![CDATA[GSSG]]></category>
		<category><![CDATA[NADPH]]></category>
		<category><![CDATA[selenocysteine]]></category>
		<category><![CDATA[selenodiglutathione]]></category>
		<category><![CDATA[TcTR]]></category>
		<category><![CDATA[Thioredoxin]]></category>
		<category><![CDATA[Thioredoxin-reductase]]></category>
		<category><![CDATA[TRX]]></category>
		<category><![CDATA[TRXR]]></category>
		<category><![CDATA[trypanothione reductase]]></category>
		<category><![CDATA[TXNRD1_V3]]></category>
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					<description><![CDATA[  Thioredoxin reductase (EC 1.6.4.5) TXNRD1 (Alternate Symbols: GRIM-12, TR, TRXR) chromosomal position 12q23.3-q24.1 (§, ‡) is a homodimeric selenocysteine-containing enzyme. Secys a selenocysteine residue is an essential TR isozyme component, located near the C-terminus region [cysteine (Cys)-497,Secys-498] of the intracellular, redox cellular environments center in the catalytically active enzyme site, Gly-499 is the actual [&#8230;]]]></description>
		
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			<media:title type="html">1w1e MITOCHONDRIAL</media:title>
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			<media:title type="html">3qfb</media:title>
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			<media:title type="html">3qfb-3h8q</media:title>
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		<item>
		<title>Catalase, the antioxidant heme enzyme one of three subgroups related to catalase deficiency in humans modulating the normal catalase reaction dependent on NADPH-binding catalases for function.</title>
		<link>https://faroucheombre.wordpress.com/2014/11/24/catalase-the-antioxidant-heme-enzyme-one-of-three-subgroups-related-to-catalase-deficiency-in-humans-modulating-the-normal-catalase-reaction-dependent-on-nadph-binding-catalases-for-function/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Mon, 24 Nov 2014 22:47:59 +0000</pubDate>
				<category><![CDATA[H2O2]]></category>
		<category><![CDATA[NADP]]></category>
		<category><![CDATA[NADPH]]></category>
		<category><![CDATA[peroxiredoxin]]></category>
		<category><![CDATA[SOD1]]></category>
		<category><![CDATA[TXN]]></category>
		<category><![CDATA[TXNRD1]]></category>
		<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[catalase]]></category>
		<category><![CDATA[Cytokine]]></category>
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					<description><![CDATA[Catalase (CAT) is converted by decomposition and intracellular localization relationships of the main cellular antioxidant enzyme system like superoxide dismutase (SOD), peroxiredoxins (Prdx), and glutathione peroxidase (GPX) are peroxisomal matrix enzymes in the cytoplasm, translocated to the peroxisomes to catalyze hydrogen peroxide H2O2 which is decomposed to oxygen and water, locus: 11p13 (§, ‡). Unlike [&#8230;]]]></description>
		
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			<media:title type="html">catalase</media:title>
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			<media:title type="html">catalase</media:title>
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		<title>Characterization of human thioredoxin system and the potential cellular responses encoded to observe the Thioredoxin-Trx1 reversibly regulated redox sites.</title>
		<link>https://faroucheombre.wordpress.com/2014/07/16/characterization-of-human-thioredoxin-system-and-the-potential-cellular-responses-encoded-to-observe-the-thioredoxin-trx1-reversibly-regulated-redox-sites/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Wed, 16 Jul 2014 18:35:25 +0000</pubDate>
				<category><![CDATA[GCG]]></category>
		<category><![CDATA[GSH glutathione]]></category>
		<category><![CDATA[GST glutathione]]></category>
		<category><![CDATA[H2O2]]></category>
		<category><![CDATA[NQO]]></category>
		<category><![CDATA[peroxiredoxin]]></category>
		<category><![CDATA[SOD1]]></category>
		<category><![CDATA[TRX]]></category>
		<category><![CDATA[TXN]]></category>
		<category><![CDATA[UGA]]></category>
		<category><![CDATA[universal automaton]]></category>
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					<description><![CDATA[Thioredoxin: human TXN, is a oxidoreductase enzyme in the status of a 12 kDa cellular redox-reductase reaction (70-kDa in bacteria, fungi and plants), a cellular defense mechanisms against oxidative stress of the cell, and numerous cytosolic processes in all cells. Txn1 is a pleiotropic cellular causative gene factor which has numerous functions. Chromosome 3p12-p11 shares [&#8230;]]]></description>
		
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			<media:title type="html">NADP</media:title>
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			<media:title type="html">1XOB</media:title>
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			<media:title type="html">enlarge</media:title>
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			<media:title type="html">NADP</media:title>
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			<media:title type="html">Zerumbone-loaded nanostructured lipid        carriers Int J Nanomedicine. 2013;8:2769-81. doi:        10.2147/IJN.S45313. Epub 2013 Aug 2 PMID:23946649 [PubMed -        indexed for MEDLINE] PMCID:PMC3739459</media:title>
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		<title>Gluathione peroxidase (GSH-Px1-GPX1) a extracellular selenoenzyme expression modulates xenobiotic metabolising enzymes.</title>
		<link>https://faroucheombre.wordpress.com/2014/04/14/gluathione-peroxidase-gsh-px1-gpx1-a-extracellular-selenoenzyme-expression-modulates-xenobiotic-metabolising-enzymes/</link>
					<comments>https://faroucheombre.wordpress.com/2014/04/14/gluathione-peroxidase-gsh-px1-gpx1-a-extracellular-selenoenzyme-expression-modulates-xenobiotic-metabolising-enzymes/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Mon, 14 Apr 2014 02:54:28 +0000</pubDate>
				<category><![CDATA[GCG]]></category>
		<category><![CDATA[GPx1]]></category>
		<category><![CDATA[GSH glutathione]]></category>
		<category><![CDATA[GST glutathione]]></category>
		<category><![CDATA[H2O2]]></category>
		<category><![CDATA[SOD1]]></category>
		<category><![CDATA[UGA]]></category>
		<category><![CDATA[universal automaton]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4904</guid>

					<description><![CDATA[     Glutathione peroxidase (EC 1.11.1.9) protects against oxidative damage via the chemoprotective action of nitric-oxide mediated lipid peroxidation and anti oxidative defense by gluathione (GSH-Px1-GPX1) a extracellular selenoenzyme, extracellular glutathione peroxidase (E-GPx) and cellular (C-GPx) detoxifies hydroperoxides. Other antioxidant genes (AOX) as Gpx1, is located in the cytosol and in (mt) mitochondria. Epithelial antioxidative enzymes (AOEs) [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">gpx1</media:title>
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			<media:title type="html">gpx1</media:title>
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		<title>G6PD, Exon 12 is an exonic splicing silencer containing/substituted define codon regions involved in the G6PD mRNA¹</title>
		<link>https://faroucheombre.wordpress.com/2013/12/31/g6pd-exon-12-is-an-exonic-splicing-silencer-containingsubstituted-define-codon-regions-involved-in-the-g6pd-mrna%c2%b9/</link>
					<comments>https://faroucheombre.wordpress.com/2013/12/31/g6pd-exon-12-is-an-exonic-splicing-silencer-containingsubstituted-define-codon-regions-involved-in-the-g6pd-mrna%c2%b9/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Tue, 31 Dec 2013 01:09:30 +0000</pubDate>
				<category><![CDATA[G6PD]]></category>
		<category><![CDATA[GPx1]]></category>
		<category><![CDATA[GSH glutathione]]></category>
		<category><![CDATA[GST glutathione]]></category>
		<category><![CDATA[HMG box]]></category>
		<category><![CDATA[NADP]]></category>
		<category><![CDATA[NADPH]]></category>
		<category><![CDATA[UGT1A1]]></category>
		<category><![CDATA[Glucose-6-phosphate dehydrogenase]]></category>
		<category><![CDATA[IKBKG]]></category>
		<category><![CDATA[Nicotinamide adenine dinucleotide phosphate]]></category>
		<category><![CDATA[Pentose phosphate pathway]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4895</guid>

					<description><![CDATA[G6PD (EC 1.1.1.49) glucose-6-phosphate dehydrogenase [§§; †, ‡], situated at Xq28 locus-coding region is the rate&#8211;limiting enzyme, of the (PPP) pentose phosphate pathway. G6PD deficiency  and its  X-linked gene mutations exons 2-13 (160 different mutations) are the most common inborn error of metabolism, in human red blood cell (RBC) enzymopathy, among humans. G6PD is divided [&#8230;]]]></description>
		
					<wfw:commentRss>https://faroucheombre.wordpress.com/2013/12/31/g6pd-exon-12-is-an-exonic-splicing-silencer-containingsubstituted-define-codon-regions-involved-in-the-g6pd-mrna%c2%b9/feed/</wfw:commentRss>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">g6pd</media:title>
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			<media:title type="html">g6pd</media:title>
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		<item>
		<title>Intra- and interchromosomal interactions of point mutations occurring in the vicinity of the normal 5-and 3 ends via low and high O(2)-affinities on the beta-globin complex.</title>
		<link>https://faroucheombre.wordpress.com/2013/09/10/intra-and-interchromosomal-interactions-of-point-mutations-occurring-in-the-vicinity-of-the-normal-5-and-3-ends-via-low-and-high-o2-affinities-on-the-beta-globin-complex/</link>
					<comments>https://faroucheombre.wordpress.com/2013/09/10/intra-and-interchromosomal-interactions-of-point-mutations-occurring-in-the-vicinity-of-the-normal-5-and-3-ends-via-low-and-high-o2-affinities-on-the-beta-globin-complex/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Tue, 10 Sep 2013 05:32:29 +0000</pubDate>
				<category><![CDATA[GATA-1]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<category><![CDATA[beta-globin]]></category>
		<category><![CDATA[CTCF]]></category>
		<category><![CDATA[GATA1]]></category>
		<category><![CDATA[HBB]]></category>
		<category><![CDATA[Red blood cell]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4885</guid>

					<description><![CDATA[Beta-globin (HBB) locus: 11p15.4  [§§; †, ‡-(HbS)] intra- and interchromosomal interactions with element in the beta-globin HBB is one of the 2 types of an asymmetric purine : pyrimidine sequences in beta-thalassemia patients (Hydroxyurea) and normal (nonthalassemic) individuals from the standard neutral – model, to any one or more of 200 different mutations (unstable free [&#8230;]]]></description>
		
					<wfw:commentRss>https://faroucheombre.wordpress.com/2013/09/10/intra-and-interchromosomal-interactions-of-point-mutations-occurring-in-the-vicinity-of-the-normal-5-and-3-ends-via-low-and-high-o2-affinities-on-the-beta-globin-complex/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			<georss:point>19.556917 -154.890131</georss:point>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">hbb</media:title>
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			<media:title type="html">hbb</media:title>
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			<media:title type="html">hbb</media:title>
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			<media:title type="html">hbb</media:title>
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			<media:title type="html">hbb</media:title>
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			<media:title type="html">hbb</media:title>
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			<media:title type="html">hbb</media:title>
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		<title>A DNA-binding protein GATA1 with a  biological unit FOG1 Zinc finger Protein molecule  is &#8216;synergistic&#8217; to the region of the X chromosome which occurred at a exome splice site X-linked involving the GATA-type zinc finger domain.</title>
		<link>https://faroucheombre.wordpress.com/2013/06/08/a-dna-binding-protein-gata1-with-a-biological-unit-fog1-zinc-finger-protein-molecule-is-synergistic-to-the-region-of-the-x-chromosome-which-occurred-at-a-exome-splice-site-x-linked-involving-the/</link>
					<comments>https://faroucheombre.wordpress.com/2013/06/08/a-dna-binding-protein-gata1-with-a-biological-unit-fog1-zinc-finger-protein-molecule-is-synergistic-to-the-region-of-the-x-chromosome-which-occurred-at-a-exome-splice-site-x-linked-involving-the/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sat, 08 Jun 2013 21:49:08 +0000</pubDate>
				<category><![CDATA[ZFPM1]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4870</guid>

					<description><![CDATA[The human ERYF1 gene (summary) NF-E1 DNA-binding protein GATA1, locus Xp11.23 [§§; †] containing 2 &#8216;finger&#8217; motifs referred to as ERYF1 of an erythroid-specific gene. The cDNA for the human ERYF1 gene is almost identical to that of chicken and mouse GATA1 gene consisting of 2 zinc finger&#8217; type motifs its activator domain contains the binding [&#8230;]]]></description>
		
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			<slash:comments>1</slash:comments>
		
		
			<georss:point>19.556917 -154.890131</georss:point>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">sequence [AT]GATA[AG] upper left</media:title>
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			<media:title type="html">4 Angstroms of PDB 1GAT in this 4 Angstrom PDB 3VD6 r</media:title>
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			<media:title type="html">gata1 biological unit ara-C (Arabinofuranosylcytosine) Cytarabine (CID_6253; SDF File (.sdf)) = ara-c (MMDB ID: 23600 PDB ID: 1P5Z)</media:title>
		</media:content>

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			<media:title type="html">Swiss PDB-viewer SPDBV</media:title>
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		<item>
		<title>Spectrin alpha, erythrocytic 1 isoform GATA1 strand B cDNA containing the EF hand domain of P17678- GATA3 and a heterodimer assembly complexed with transmembrane SCF neural cell (Slc4a1) band 3 aspect of the alpha complex analogue Spna1.</title>
		<link>https://faroucheombre.wordpress.com/2013/03/03/spectrin-alpha-erythrocytic-1-isoform-gata1-strand-b-cdna-containing-the-ef-hand-domain-of-p17678-gata3-and-a-heterodimer-assembly-complexed-with-transmembrane-scf-neural-cell-slc4a1-band-3-aspect/</link>
					<comments>https://faroucheombre.wordpress.com/2013/03/03/spectrin-alpha-erythrocytic-1-isoform-gata1-strand-b-cdna-containing-the-ef-hand-domain-of-p17678-gata3-and-a-heterodimer-assembly-complexed-with-transmembrane-scf-neural-cell-slc4a1-band-3-aspect/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sun, 03 Mar 2013 21:25:32 +0000</pubDate>
				<category><![CDATA[Epo]]></category>
		<category><![CDATA[EST]]></category>
		<category><![CDATA[GATA-1]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4814</guid>

					<description><![CDATA[Spectrin alpha, erythrocytic 1 [ Mus musculus ] [§§; †, ‡] anchored to the cytoplasmic face of the plasma membrane via ankyrin, which binds to beta-spectrin and is  affecting the conversion of spectrin dimers to tetramers erythroid alpha- or beta-spectrin &#8211; Retrotransposon long terminal repeat 3&#8242; LTR alpha 1 and the 5&#8242; LTR alpha 2 [&#8230;]]]></description>
		
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			<slash:comments>4</slash:comments>
		
		
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">SPNA1 PDB:1OWA Protein PDB: 1HYN Band 3, and GATA1 DNA strand B PDB:1GAT</media:title>
		</media:content>
	</item>
		<item>
		<title>Spnb2 protein family architecture perspective and differences in complex form of exon/intron usage</title>
		<link>https://faroucheombre.wordpress.com/2013/02/12/spnb2-protein-family-architecture-perspective-and-differences-in-complex-form-of-exonintron-usage/</link>
					<comments>https://faroucheombre.wordpress.com/2013/02/12/spnb2-protein-family-architecture-perspective-and-differences-in-complex-form-of-exonintron-usage/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Tue, 12 Feb 2013 20:40:10 +0000</pubDate>
				<category><![CDATA[beta2]]></category>
		<category><![CDATA[phosphatidylinositol]]></category>
		<category><![CDATA[SH3]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4790</guid>

					<description><![CDATA[Spectrin isoforms are found in erythroid and nonerythroid cells. Spectrin is a component (known as the postsynaptic density (PSD)) for the maintenance of cell  cytoskeleton shape  the main fibrous component of which is spectrin of the erythrocyte membrane controlling Smad3/4 subcellular localization in TGFβ/Smad signalling resulting in nuclear translocation  of activated Smad4. Nonerythroid brain spectrin [&#8230;]]]></description>
		
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			<slash:comments>2</slash:comments>
		
		
			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">Figure 3: Spnb2 instances of intron/exon usage</media:title>
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	</item>
		<item>
		<title>Human TGF-beta Type II Receptor</title>
		<link>https://faroucheombre.wordpress.com/2013/01/01/human-tgf-beta-type-ii-receptor/</link>
					<comments>https://faroucheombre.wordpress.com/2013/01/01/human-tgf-beta-type-ii-receptor/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Tue, 01 Jan 2013 21:43:45 +0000</pubDate>
				<category><![CDATA[dynein]]></category>
		<category><![CDATA[ECM extracellular matrix]]></category>
		<category><![CDATA[epigallocatechin]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[Complementary DNA]]></category>
		<category><![CDATA[Genetics]]></category>
		<category><![CDATA[Messenger RNA]]></category>
		<category><![CDATA[TGF beta receptors]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4755</guid>

					<description><![CDATA[TGFBR type II receptors (TGFBR2) are transmembrane tyrosine kinases or associated with cytoplasmic tyrosine kinases** related to resistance to TGF-beta inhibition of cell proliferation and trap TGF-beta I from access to wild-type receptors, the growth-inhibitory and proapoptotic activities of the cytokine, human chromosome 3p22-p21: [§§; †, ‡]. A cysteine&#8211;rich wildtypeº SNP-(ancestral C-509T-allele and G-875A variant in [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">human TbetaR2 ectodomain--TGF-beta3 complex with ELF-3DNA</media:title>
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		<media:content url="https://lh4.googleusercontent.com/-VOis9ZagayA/UODv4TTaXVI/AAAAAAAADlI/Pg1VV_LN0vk/s640/influblk.png" medium="image">
			<media:title type="html">Influenza virus to maintain 3d cohesion of delivery (EGCG) binds with the anti-cancer drug Bortezomib=PMID:17634290</media:title>
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		<media:content url="https://lh3.googleusercontent.com/-_w-UzTcx37g/UOO97ucBxPI/AAAAAAAADn4/19AEJTntE2U/s576/borin2.png" medium="image">
			<media:title type="html">ESE ELF3 (ESE1/ESX), ets transcription factor binds to the TGF-beta RII promoter. Autophosphorylation</media:title>
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		<item>
		<title>Transforming growth factor beta 1</title>
		<link>https://faroucheombre.wordpress.com/2012/11/22/transforming-growth-factor-beta-1/</link>
					<comments>https://faroucheombre.wordpress.com/2012/11/22/transforming-growth-factor-beta-1/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Thu, 22 Nov 2012 22:03:04 +0000</pubDate>
				<category><![CDATA[FK506]]></category>
		<category><![CDATA[phosphatidylinositol]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<category><![CDATA[TGFB]]></category>
		<category><![CDATA[Endoglin]]></category>
		<category><![CDATA[Smad]]></category>
		<category><![CDATA[TGF beta receptors]]></category>
		<category><![CDATA[Transforming growth factor beta]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4742</guid>

					<description><![CDATA[TGFBR1 are transmembrane tyrosine kinases or associated with cytoplasmic tyrosine kinase TGF-β&#8216;s » specificity with type II receptors activating type I receptors, has the pre-helix extension and its role in binding are present on the plasma membrane (cytoplasmic domain) both as monomers and homo- and hetero-oligomers chromosome 9q22.33. 6 : [§§; †, ‡]. Activin receptor-like [&#8230;]]]></description>
		
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		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
		</media:content>

		<media:content url="http://2.bp.blogspot.com/-yQ5aYaTTNxc/UK6UNU3Va9I/AAAAAAAADjQ/fuBBSURG6jc/s320/+2+TGFBR1+molecules+ternary.png" medium="image" />
	</item>
		<item>
		<title>CRYSTAL STRUCTURE OF ACTIVIN RECEPTOR TYPE II KINASE DOMAIN FROM HOMO SAPIENS</title>
		<link>https://faroucheombre.wordpress.com/2012/08/30/crystal-structure-of-activin-receptor-type-ii-kinase-domain-from-homo-sapiens/</link>
					<comments>https://faroucheombre.wordpress.com/2012/08/30/crystal-structure-of-activin-receptor-type-ii-kinase-domain-from-homo-sapiens/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Thu, 30 Aug 2012 21:05:32 +0000</pubDate>
				<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[BMP]]></category>
		<category><![CDATA[Smad]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<category><![CDATA[Transforming growth factor beta]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4735</guid>

					<description><![CDATA[ACVR2B of type I and IB the major mRNA species found during reproductive development, type II and IIA structurally related activin receptors Locus: 3p22.2 : [§§; †] and activates its serine/threonine kinase type-2 receptor then phosphorylates and activates (required for extracellular ligand binding the myostatin* signaling pathway), &#8216;the type-1&#8242; (BMPs)  via a different set of [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
		</media:content>

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			<media:title type="html">TITLE CRYSTAL STRUCTURE OF ACTIVIN RECEPTOR TYPE II KINASE DOMAIN TITLE 2 FROM HUMAN</media:title>
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	</item>
		<item>
		<title>FLRG (follistatin-related gene; 3)</title>
		<link>https://faroucheombre.wordpress.com/2012/07/17/flrg-follistatin-related-gene-3/</link>
					<comments>https://faroucheombre.wordpress.com/2012/07/17/flrg-follistatin-related-gene-3/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Tue, 17 Jul 2012 09:27:30 +0000</pubDate>
				<category><![CDATA[BMP]]></category>
		<category><![CDATA[phosphatidylinositol]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<category><![CDATA[FLRG]]></category>
		<category><![CDATA[Osteonectin]]></category>
		<category><![CDATA[Smad]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4731</guid>

					<description><![CDATA[&#160; Follistatin/Osteonectin-like EGF domain, the FSTL3 gene chromosome 19p13: [§§; †, ␠]. FLRG (follistatin-related gene; 3) found to be stored in secretory granules of the cells, encodes contains 2 cysteine-rich secretory proteins functioning as a secreted glycoprotein once bound to 2 potential N-glycosylation sites an exon/intron domain structure both the activin domain its propeptide (WFIKKN2) [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">figure 1 Follistatin/Osteonectin-like EGF domain</media:title>
		</media:content>
	</item>
		<item>
		<title>Myostatin as part of a latent complex in the vicinity of the (D) polymorphism MSTN</title>
		<link>https://faroucheombre.wordpress.com/2012/05/29/myostatin-as-part-of-a-latent-complex-in-the-vicinity-of-the-d-polymorphism-mstn/</link>
					<comments>https://faroucheombre.wordpress.com/2012/05/29/myostatin-as-part-of-a-latent-complex-in-the-vicinity-of-the-d-polymorphism-mstn/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Tue, 29 May 2012 06:02:33 +0000</pubDate>
				<category><![CDATA[Kunitz-type genes]]></category>
		<category><![CDATA[TGF-beta]]></category>
		<category><![CDATA[TGFB]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4726</guid>

					<description><![CDATA[Myostatin , also known as growth and differentiation factor 8 (GDF8) a TGF-beta family member is (an inhibitor of myogenesis) secreted into the plasma expressed in human skeletal muscle (expressed in many different muscles throughout the body) as a 12.5-kD propeptide and a 26-kD glycoprotein (myostatin-immunoreactive protein) a dimer (three exons and two introns) locus: 2q32.2 [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
		</media:content>

		<media:content url="https://lh3.googleusercontent.com/-5v1zdBSnAoI/T8QdLj5oCbI/AAAAAAAADaU/hg_rFV7wkmY/s720/allpre1.png" medium="image">
			<media:title type="html">3hh2-(Myostatin) of known structure IPR008197 Whey_acidic_protein</media:title>
		</media:content>

		<media:content url="https://lh3.googleusercontent.com/-6hjkbVvtIlg/T8QOyd0de1I/AAAAAAAADYI/bUcjNOk1NlE/s800/selene2.png" medium="image">
			<media:title type="html">2p6a with the two neighboring molecules 2p6A 3hh2 and 3hh2a in the vicinity of the (D) polymorphism MSTN of the consensus motif</media:title>
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	</item>
		<item>
		<title>DOMAIN OF AREA COMPLEXED GLP-1_GLP1R_GCG_EXENDIN-4 REGION IF INTERACTION RECEPTOR VARIANTS</title>
		<link>https://faroucheombre.wordpress.com/2012/05/28/domain-of-area-complexed-glp-1_glp1r_gcg_exendin-4-region-if-interaction-receptor-variants/</link>
					<comments>https://faroucheombre.wordpress.com/2012/05/28/domain-of-area-complexed-glp-1_glp1r_gcg_exendin-4-region-if-interaction-receptor-variants/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Mon, 28 May 2012 06:34:17 +0000</pubDate>
				<category><![CDATA[GPCR]]></category>
		<category><![CDATA[Exenatide]]></category>
		<category><![CDATA[Gastric inhibitory polypeptide]]></category>
		<category><![CDATA[Glucagon-like peptide-1]]></category>
		<category><![CDATA[Incretin]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4708</guid>

					<description><![CDATA[GLP1 receptor (GLP1R) a seven-transmembrane family B G protein-coupled receptor (GPCR) locus : 6p21.2 [§§; ^], with a N-terminal extracellular domain is a potent insulinotropic incretin hormone important in maintaining blood glucose homeostasis, through their receptors, GLP1R and glucose-dependent insulinotropic polypeptide GIPR. The glucagon-like peptide-1 (GLP-1) C-terminal regions bind to the N terminus (NTD) this [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
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		<media:content url="http://upload.wikimedia.org/wikipedia/commons/thumb/7/77/Protein_GLP1R_PDB_3C59.png/75px-Protein_GLP1R_PDB_3C59.png" medium="image">
			<media:title type="html">English: Structure of protein GLP1R.Based on P...</media:title>
		</media:content>

		<media:content url="https://lh6.googleusercontent.com/-Ev9vaPCqHio/T7L34n851pI/AAAAAAAADXU/IyQVXaeOXkQ/s720/helixloopc.png" medium="image">
			<media:title type="html">Figure:1_Crystal Structure Of Glucagon-Like Peptide-1 In Complex With The Extracellular Domain Of The Glucagon-Like Peptide-1 Receptor_Figure:3 &#038; 4</media:title>
		</media:content>
	</item>
		<item>
		<title>TCL7L2 traits and activity that affect its expression</title>
		<link>https://faroucheombre.wordpress.com/2012/04/26/tcl7l2-traits-and-activity-that-affect-its-expression/</link>
					<comments>https://faroucheombre.wordpress.com/2012/04/26/tcl7l2-traits-and-activity-that-affect-its-expression/#comments</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Thu, 26 Apr 2012 04:52:25 +0000</pubDate>
				<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[Allele]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[DNA]]></category>
		<category><![CDATA[Gene]]></category>
		<category><![CDATA[Genotype]]></category>
		<category><![CDATA[Single-nucleotide polymorphism]]></category>
		<category><![CDATA[TCF7L2]]></category>
		<category><![CDATA[Wnt signaling pathway]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4705</guid>

					<description><![CDATA[TCL7L2 Transcription factor 7-like 2 acts through regulation of proglucagon (GLP-1R) in enteroendocrine cells implicated in blood glucose homeostasis also called TCF4 of the four members of the downstream effector of Wnt signaling T-cell factor (TCF ) to human chromosome band 10q25.2, 25.3 : [§§; ^].  Noninsulin-dependent, susceptibality to TCF7L2, IVS3, C&#8211;T  polymorphisms* (and high-risk [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
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			<media:title type="html">emissrto</media:title>
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		<media:content url="https://lh5.googleusercontent.com/-fogVbnUT-DU/T5i_havH9lI/AAAAAAAADPw/um6n-f45l-A/s640/ncbi-lys-1jdh2.png" medium="image">
			<media:title type="html">TCL7L2 transcription factor 7-like 2 (T-cell specific, HMG-box) Ribbon diagram showing the overlay (CTNNB1 NCBI.pdb</media:title>
		</media:content>

		<media:content url="https://lh3.googleusercontent.com/-TrY2zeQbdEI/T5i_i-3f-PI/AAAAAAAADP4/e7brpH2P33o/s640/lef1-1g3j-1jdh-lys2.png" medium="image">
			<media:title type="html">Figure (2.) TCF4 with 2LEF DNA oriefted to figure (1.) Crystal Structure Of A Human Tcf-4 BETA-Catenin Complex</media:title>
		</media:content>
	</item>
		<item>
		<title>CTNNB1 catenin (cadherin-associated protein), beta 1 and formation of branching point structures beta-catenin / LEF demonstrating nucleation at TBE1 site (TCF7L2)</title>
		<link>https://faroucheombre.wordpress.com/2012/03/25/ctnnb1-catenin-cadherin-associated-protein-beta-1-and-formation-of-branching-point-structures-beta-catenin-lef-demonstrating-nucleation-at-tbe1-site-tcf7l2/</link>
					<comments>https://faroucheombre.wordpress.com/2012/03/25/ctnnb1-catenin-cadherin-associated-protein-beta-1-and-formation-of-branching-point-structures-beta-catenin-lef-demonstrating-nucleation-at-tbe1-site-tcf7l2/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sun, 25 Mar 2012 22:44:52 +0000</pubDate>
				<category><![CDATA[APC]]></category>
		<category><![CDATA[CDH1]]></category>
		<category><![CDATA[GLI3/ssh]]></category>
		<category><![CDATA[Axin]]></category>
		<category><![CDATA[CDH1 (gene)]]></category>
		<category><![CDATA[CTNNB1]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4698</guid>

					<description><![CDATA[Catenin Beta 1, CTNNB are cell adhesion molecules called (p120*␠&#8211;catenin) cadherins (the (CDH1) E-cadherin/catenin complex) include the  beta-catenins a multifunctional molecule Locus: 3p22.1 [§§; ^]. Neurons also exhibited a higher CTNNB/TCF pathway association (concentration versus accumulation) with cadherins; CAS&#8211;chromosome segregation 1-like (yeast) binds with E-cadherin but not with beta-catenin. Which interacts with (Tcf-T-cell factor where a [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
		</media:content>

		<media:content url="https://lh6.googleusercontent.com/-YaSa95TwGaw/T2-VR583dQI/AAAAAAAADKQ/s-YqK8gRAV0/s720/3fqr.png" medium="image">
			<media:title type="html">Catenin Beta 1, CTNNB PDB:3FQR and the closely related T-cell factor 1 (TCF-1) Lymphoid enhancer-binding factor (PDB; 2LEF[-1]) as the technical DNA coil,</media:title>
		</media:content>
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		<item>
		<title>LAR, Leukocyte common antigen related, Receptor-type tyrosine-protein phosphatase F (PTPRF)</title>
		<link>https://faroucheombre.wordpress.com/2012/02/15/lar-leukocyte-common-antigen-related-receptor-type-tyrosine-protein-phosphatase-f-ptprf/</link>
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		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Wed, 15 Feb 2012 20:09:09 +0000</pubDate>
				<category><![CDATA[ptk]]></category>
		<category><![CDATA[TRIO]]></category>
		<category><![CDATA[PTK]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4680</guid>

					<description><![CDATA[The human LAR (PTPRF) gene has 2 tandemly repeated PTPase associated tandem subunit domains, locus: 1p34.2 [§§;^] and represents a receptor-type PTP (EC 3.1.3.48), through cell-cell or cell&#8211;matrix interactions processed into 2 noncovalently associated subunits RPTPs that acts as a protein-tyrosine phosphatase associate with Trk protein tyrosine kinase (PTK) receptors in the cytoplasmic segment for dephosphorylation of [&#8230;]]]></description>
		
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			<georss:point>19.556917 -154.890131</georss:point>
		<geo:lat>19.556917</geo:lat>
		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
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		<media:content url="https://lh6.googleusercontent.com/-ybsEe8VbkPg/Tzqd_s0JsvI/AAAAAAAADAQ/1WiwXXx5Hi8/s128/2e.png" medium="image">
			<media:title type="html">PDB-1LAR Associated subunits RPTPs (receptor protein tyr. phos.) that acts as a protein-tyrosine phosphatase Domain 1</media:title>
		</media:content>

		<media:content url="https://lh5.googleusercontent.com/-0lvZ1NoFMS8/Tzqd_yFTguI/AAAAAAAADAU/efObOtRR2GY/s128/2d.png" medium="image">
			<media:title type="html">placement of tyrosine phosphorylated 1LAR that is other wise in the center between the two domains D1 and D2 here on the D1 ribbon</media:title>
		</media:content>
	</item>
		<item>
		<title>Protein-tyrosine phosphatase 1B</title>
		<link>https://faroucheombre.wordpress.com/2012/01/28/protein-tyrosine-phosphatase-1b/</link>
					<comments>https://faroucheombre.wordpress.com/2012/01/28/protein-tyrosine-phosphatase-1b/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sat, 28 Jan 2012 20:33:10 +0000</pubDate>
				<category><![CDATA[Janus]]></category>
		<category><![CDATA[Cell Biology]]></category>
		<category><![CDATA[Cell membrane]]></category>
		<category><![CDATA[Endoplasmic reticulum]]></category>
		<category><![CDATA[Kinase]]></category>
		<category><![CDATA[Protein tyrosine phosphatase]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4673</guid>

					<description><![CDATA[PTPN1 nonreceptor type1 gene, which encodes PTP1B the prototypic member of the PTP family is responsible for negatively regulating insulin by dephosphorylating the phosphotyrosine (ptyr) residues* of the insulin receptor (INSR) kinase activation segment IRK (kinase domain of the insulin receptor) mainly by its association with IR localized to the plasma membrane in a Grb2 [&#8230;]]]></description>
		
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			<media:title type="html">emissrto</media:title>
		</media:content>

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			<media:title type="html">2CMC oriented towards pocket containing cysteine molecule</media:title>
		</media:content>

		<media:content url="https://lh6.googleusercontent.com/-z5bmPlMdnGU/TyRJFHABLyI/AAAAAAAAC9k/BGKfznzrYeU/s128/folder4.png" medium="image">
			<media:title type="html">PDB 2CMC double mutant</media:title>
		</media:content>
	</item>
		<item>
		<title>Non-receptor tyrosine-protein kinase TYK2</title>
		<link>https://faroucheombre.wordpress.com/2011/12/12/4662/</link>
					<comments>https://faroucheombre.wordpress.com/2011/12/12/4662/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Mon, 12 Dec 2011 01:32:48 +0000</pubDate>
				<category><![CDATA[Janus]]></category>
		<category><![CDATA[IFN]]></category>
		<category><![CDATA[Interferon]]></category>
		<category><![CDATA[Janus kinase]]></category>
		<category><![CDATA[Messenger RNA]]></category>
		<category><![CDATA[Nucleic acid sequence]]></category>
		<category><![CDATA[Signal transduction]]></category>
		<category><![CDATA[STAT protein]]></category>
		<category><![CDATA[Tyrosine kinase]]></category>
		<category><![CDATA[Tyrosine kinase 2]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4662</guid>

					<description><![CDATA[TYK2 a Janus kinase, contains a C-terminal protein tyrosine kinase catalytic domain and has no N&#8211;terminal signal peptide or transmembrane domain, of coding regions of exons and the adjacent intronic DNA sequences, identical to tyk2 of mutant Tyk2 forms deleted at the N terminus locus:19p13.2 [§§], a human mRNA (rs2304256) exon¤ encoding a non-receptor protein [&#8230;]]]></description>
		
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			<slash:comments>0</slash:comments>
		
		
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		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
		</media:content>

		<media:content url="https://lh3.googleusercontent.com/-WOPAP3r5bXs/TuVNzep4G3I/AAAAAAAAC10/x3ySmLeOTD4/s576/tyrsurf-png.svg.png" medium="image">
			<media:title type="html">TYK2 bind phosphotyrosine</media:title>
		</media:content>

		<media:content url="https://lh3.googleusercontent.com/-pxVa-txSFu4/TuVL_G3d3PI/AAAAAAAAC1U/WPwdmJvTy1Q/s720/lightputty.svg.png" medium="image">
			<media:title type="html">TYK2 the DNA-binding domain</media:title>
		</media:content>

		<media:content url="https://lh5.googleusercontent.com/-ODzrqukO1rA/TuWHJMdv4MI/AAAAAAAAC4M/cEQ2EKUrfGM/s640/hmm3NOZ2.png" medium="image">
			<media:title type="html">TYK2 of 3NZO coding regions of exons and the adjacent intronic DNA</media:title>
		</media:content>
	</item>
		<item>
		<title>STAT1 signal transducer and activator of transcription 1</title>
		<link>https://faroucheombre.wordpress.com/2011/11/27/stat1-signal-transducer-and-activator-of-transcription-1/</link>
					<comments>https://faroucheombre.wordpress.com/2011/11/27/stat1-signal-transducer-and-activator-of-transcription-1/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sun, 27 Nov 2011 03:18:14 +0000</pubDate>
				<category><![CDATA[IFNG]]></category>
		<category><![CDATA[IL1]]></category>
		<category><![CDATA[Janus]]></category>
		<category><![CDATA[p53]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[Exotoxin]]></category>
		<category><![CDATA[Interferon]]></category>
		<category><![CDATA[Interferon-gamma]]></category>
		<category><![CDATA[Nmi]]></category>
		<category><![CDATA[Signal transduction]]></category>
		<category><![CDATA[STAT protein]]></category>
		<category><![CDATA[STAT1]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4654</guid>

					<description><![CDATA[The JAK/STAT pathway signal transducer and activator of transcription STAT1 location: 2q32.2: [§§], is downstream of cytokine receptor IL2RG consisting of an N-terminal oligomerization domain surrounds a completely conserved arginine residue. And a C-terminal SRC homology-2 (SH2) domain and receptors which translocates GAF and  p48 ((protein 48), ISGF3) to the nucleus and upregulates in signal [&#8230;]]]></description>
		
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			<media:title type="html">emissrto</media:title>
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		<media:content url="https://lh3.googleusercontent.com/-UNuGmJxfFNk/TtGdO3IaxtI/AAAAAAAACwE/fQE8OD8xU8k/s720/1bf5%252520aligned%2525201yvl-svg-png%25252Cpng.png" medium="image">
			<media:title type="html">Two dimer interfaces are seen termed antiparallel or parallel 1bf5 &#038; 1yvl</media:title>
		</media:content>

		<media:content url="http://3.bp.blogspot.com/-ji-Jm-sw3Do/TtXBQTsTBEI/AAAAAAAACw0/KORzBhKEEGw/s200/dnaz1.png" medium="image">
			<media:title type="html">Tyr701 transmigration route Via 74.56</media:title>
		</media:content>

		<media:content url="http://2.bp.blogspot.com/-zQouHFfa_O4/TtY3JHPZ8MI/AAAAAAAAC0Y/0HFKi0_rJGY/s200/144pocket3png.png" medium="image">
			<media:title type="html"> Tyr701 note the two orange ** tags </media:title>
		</media:content>

		<media:content url="http://2.bp.blogspot.com/-PhYTo5-CVq8/TtYK9b0_8mI/AAAAAAAACzE/pWCntE_LX0Q/s200/126.42tyr701svg.png" medium="image">
			<media:title type="html">antigen-driven proinflammatory immune responses in &#039;addition&#039; contribute to</media:title>
		</media:content>

		<media:content url="http://scq.ubc.ca/sciencescouts/42medical.jpg" medium="image">
			<media:title type="html">science has forced me to engineer medical attention 4  &#034;idiotypic vaccines &#038; other humanized methods</media:title>
		</media:content>
	</item>
		<item>
		<title>Tyrosine-protein kinase JAK1</title>
		<link>https://faroucheombre.wordpress.com/2011/11/09/4646/</link>
					<comments>https://faroucheombre.wordpress.com/2011/11/09/4646/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Wed, 09 Nov 2011 02:31:19 +0000</pubDate>
				<category><![CDATA[14-3-3]]></category>
		<category><![CDATA[IL6]]></category>
		<category><![CDATA[ptk]]></category>
		<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[Cytokine]]></category>
		<category><![CDATA[Immunology]]></category>
		<category><![CDATA[Janus]]></category>
		<category><![CDATA[Janus kinase]]></category>
		<category><![CDATA[Leukemia inhibitory factor]]></category>
		<category><![CDATA[Oncostatin M receptor]]></category>
		<category><![CDATA[Signal transduction]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4646</guid>

					<description><![CDATA[The Janus kinase family, Type I and II cytokine receptors is immediately N-terminal to the PTK domain  1p31.3: [§§]. And JAK2 in the interferon-gamma pathway PTK activity is located in the C-terminal PTK&#8216;-like domain has a negative role of an intrinsic JAK inhibitor suppressor of cytokine signaling (Cordyceps bassiana&#8216; may contain more than one active [&#8230;]]]></description>
		
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			<media:title type="html">emissrto</media:title>
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			<media:title type="html">JAK1 PTK domain in complex with two JAK inhibitors</media:title>
		</media:content>
	</item>
		<item>
		<title>Oncostatin M a member of the IL-6 family of cytokines</title>
		<link>https://faroucheombre.wordpress.com/2011/10/12/oncostatin-m-a-member-of-the-il-6-family-of-cytokines/</link>
					<comments>https://faroucheombre.wordpress.com/2011/10/12/oncostatin-m-a-member-of-the-il-6-family-of-cytokines/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Wed, 12 Oct 2011 21:35:31 +0000</pubDate>
				<category><![CDATA[AP-1]]></category>
		<category><![CDATA[gp160]]></category>
		<category><![CDATA[IL6]]></category>
		<category><![CDATA[TATA]]></category>
		<category><![CDATA[universal automaton]]></category>
		<category><![CDATA[VEGF]]></category>
		<category><![CDATA[Cytokine]]></category>
		<category><![CDATA[Glycoprotein 130]]></category>
		<category><![CDATA[Immunology]]></category>
		<category><![CDATA[Interleukin 6]]></category>
		<category><![CDATA[Leukemia inhibitory factor]]></category>
		<category><![CDATA[LIF]]></category>
		<category><![CDATA[Oncostatin M]]></category>
		<category><![CDATA[OSM]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4639</guid>

					<description><![CDATA[Oncostatin M is a member of the IL-6 family of cytokines. OSM regulates the growth and differentiation of a number of tumor and normal cells. OSM, like LIF, is located on human chromosome 22, human OSM activates the LIF receptor heterodimer, containing defined regions of human chromosome 2q12.2: [§§]. OSM exclusively uses the OSMR* Oncostatin M [&#8230;]]]></description>
		
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		<geo:long>-154.890131</geo:long>
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			<media:title type="html">emissrto</media:title>
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		<media:content url="http://upload.wikimedia.org/wikipedia/en/thumb/7/70/Hosm.jpg/300px-Hosm.jpg" medium="image">
			<media:title type="html">Ribbon representation of oncostatin M showing ...</media:title>
		</media:content>
	</item>
		<item>
		<title>The interleukin-6 signal transducer, gp130</title>
		<link>https://faroucheombre.wordpress.com/2011/09/21/the-interleukin-6-signal-transducer-gp130/</link>
					<comments>https://faroucheombre.wordpress.com/2011/09/21/the-interleukin-6-signal-transducer-gp130/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Wed, 21 Sep 2011 22:21:20 +0000</pubDate>
				<category><![CDATA[gp160]]></category>
		<category><![CDATA[IL6]]></category>
		<category><![CDATA[Janus]]></category>
		<category><![CDATA[pg]]></category>
		<category><![CDATA[Agar]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[Ciliary neurotrophic factor]]></category>
		<category><![CDATA[Glycoprotein 130]]></category>
		<category><![CDATA[Interleukin 6]]></category>
		<category><![CDATA[Leukemia inhibitory factor]]></category>
		<category><![CDATA[Oncostatin M]]></category>
		<category><![CDATA[Signal transduction]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4621</guid>

					<description><![CDATA[The interleukin-6 signal transducer, gp130 the signal-transducing receptor chain of interleukin-6-type cytokines, IL6ST was assigned to chromosome 5q11.2: [§§], is a shared transducer chain triggered by homodimerization (IL6) on the plasma membrane IL-6-trans-signaling is counter balanced by a naturally occurring, soluble form of gp130 (sgp130) or heterodimerization with LIF-Rb/gp190 protein (IL11 has three distinct receptor [&#8230;]]]></description>
		
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		<media:content url="http://upload.wikimedia.org/wikipedia/commons/thumb/c/cb/GP130_Crystal_Structure.rsh.png/300px-GP130_Crystal_Structure.rsh.png" medium="image">
			<media:title type="html">Crystal structure of gp130 as published in the...</media:title>
		</media:content>
	</item>
		<item>
		<title>Leukemia inhibitory factor LIF and the presence of other growth factors at the interface of a shared cell-surface signaling receptor.</title>
		<link>https://faroucheombre.wordpress.com/2011/09/05/leukemia-inhibitory-factor-lif-and-the-presence-of-other-growth-factors-at-the-interface-of-a-shared-cell-surface-signaling-receptor/</link>
					<comments>https://faroucheombre.wordpress.com/2011/09/05/leukemia-inhibitory-factor-lif-and-the-presence-of-other-growth-factors-at-the-interface-of-a-shared-cell-surface-signaling-receptor/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Mon, 05 Sep 2011 05:45:33 +0000</pubDate>
				<category><![CDATA[BMP]]></category>
		<category><![CDATA[Janus]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[Biotechnology]]></category>
		<category><![CDATA[Cytokine]]></category>
		<category><![CDATA[Embryonic stem cell]]></category>
		<category><![CDATA[Immunology]]></category>
		<category><![CDATA[Leukemia inhibitory factor]]></category>
		<category><![CDATA[Proopiomelanocortin]]></category>
		<category><![CDATA[Stem cell]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4615</guid>

					<description><![CDATA[A protein variously termed leukemia inhibitory factor LIF locus : 22q12.2 [§§], exhibits pleiotropic biological activities, it plays a critical role in several endocrine functions including acting in synergy with other cytokines LIF and  BMP2 [2.] being in the centre of interest for doping abusers, equivalent to that observed in the presence of LIF alone [&#8230;]]]></description>
		
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		<media:content url="https://lh4.googleusercontent.com/-aDnUHHcZtaU/TmRFPWH67VI/AAAAAAAACrc/wscMCTTSkJs/s288/2Q7N-snapshot-800x800-31490.png" medium="image">
			<media:title type="html">LIF as prototypes (neurally active cytokine LIF), four helix bundle cytokines form, a functional receptor complex</media:title>
		</media:content>
	</item>
		<item>
		<title>FPR ligands a G protein-coupled receptor</title>
		<link>https://faroucheombre.wordpress.com/2011/08/25/fpr-ligands-a-g-protein-coupled-receptor/</link>
					<comments>https://faroucheombre.wordpress.com/2011/08/25/fpr-ligands-a-g-protein-coupled-receptor/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Thu, 25 Aug 2011 17:40:52 +0000</pubDate>
				<category><![CDATA[B12]]></category>
		<category><![CDATA[FK506]]></category>
		<category><![CDATA[GPCR]]></category>
		<category><![CDATA[IL8]]></category>
		<category><![CDATA[Adrenergic receptor]]></category>
		<category><![CDATA[Biochemistry and Molecular Biology]]></category>
		<category><![CDATA[Biology]]></category>
		<category><![CDATA[Biomolecules]]></category>
		<category><![CDATA[G protein-coupled receptor]]></category>
		<category><![CDATA[Peptide]]></category>
		<category><![CDATA[Proteins and Enzymes]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4611</guid>

					<description><![CDATA[The fMet-Leu-Phe (fMLP) receptor FMLP locus: 19q13.4 : [§§] or FPRL1 a mouse counterpart of FPRL1R (the peptide ligand Trp-Lys-Tyr-Met-Val-L-Met-NH(2) a synthetic peptide, WKYMVM uPAR epitope uPAR84-95, is an endogenous ligand for FPRL2 and FPRL1)  two closely related G-protein coupled receptors interact with viral and bacterial N-formyl peptides, peptides derived from the  N-terminal domain of [&#8230;]]]></description>
		
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			<media:title type="html">emissrto</media:title>
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		<media:content url="https://lh3.googleusercontent.com/-Va5FQjQog7A/TlafZRHPItI/AAAAAAAACrM/-n8DfOUdejM/http1degreebio.org.png" medium="image">
			<media:title type="html">Karma Points are 1DegreeBio&#039;s currency</media:title>
		</media:content>
	</item>
		<item>
		<title>MAL2 macrophage-activating lipopeptide 2</title>
		<link>https://faroucheombre.wordpress.com/2011/08/13/mal2-macrophage-activating-lipopeptide-2/</link>
					<comments>https://faroucheombre.wordpress.com/2011/08/13/mal2-macrophage-activating-lipopeptide-2/#respond</comments>
		
		<dc:creator><![CDATA[Mark]]></dc:creator>
		<pubDate>Sat, 13 Aug 2011 23:01:17 +0000</pubDate>
				<category><![CDATA[MARVEL]]></category>
		<category><![CDATA[universal automaton]]></category>
		<guid isPermaLink="false">http://faroucheombre.wordpress.com/?p=4603</guid>

					<description><![CDATA[MAL2 macrophage-activating lipopeptide 2, TPD52 a coiled-coil motif-bearing protein and unrecognized prostate-specific protein, PrLZ (prostate leucine zipper), to which (toll-like receptor agonist macrophage-activating lipopeptide-2) MAL2 binds, is located on chromosome 8q21.13.; [§§]. (MALP-2) is essential for transcytosis across the interior of intestinal cells-bile canaliculus (basolateral to apical) membrane region, apically localized endosome structures en route [&#8230;]]]></description>
		
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			<media:title type="html">emissrto</media:title>
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		<media:content url="https://lh3.googleusercontent.com/-ykbKN5y1oI8/Tkb3G1glIuI/AAAAAAAACrA/8s25JyidpCU/s512/1DDL-snapshot-783x783-19453z.png" medium="image">
			<media:title type="html">Desmodium yellow mottle virus Synthetic IDDL</media:title>
		</media:content>
	</item>
	</channel>
</rss>
