DNAJB9
DNAJB9 (DnaJ heat shock protein family (Hsp40) member B9) هوَ بروتين يُشَفر بواسطة جين DNAJB9 في الإنسان.[1][2][3]
المراجع
- "Mammalian HSP40/DNAJ homologs: cloning of novel cDNAs and a proposal for their classification and nomenclature"، Cell Stress Chaperones، 5 (2): 98–112، يناير 2001، doi:10.1379/1466-1268(2000)005<0098:MHDHCO>2.0.CO;2، PMC 312896، PMID 11147971.
- "Entrez Gene: DNAJB9 DnaJ (Hsp40) homolog, subfamily B, member 9"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Assignment of the microvascular endothelial differentiation gene 1 (MDG1) to human chromosome band 14q24.2→q24.3 by fluorescence in situ hybridization"، Cytogenet Cell Genet، 79 (1–2): 149–50، أبريل 1998، doi:10.1159/000134706، PMID 9533036.
قراءة متعمقة
- Zhang QH؛ Ye M؛ Wu XY؛ وآخرون (2001)، "Cloning and Functional Analysis of cDNAs with Open Reading Frames for 300 Previously Undefined Genes Expressed in CD34+ Hematopoietic Stem/Progenitor Cells"، Genome Res.، 10 (10): 1546–60، doi:10.1101/gr.140200، PMC 310934، PMID 11042152.
- Wiemann S؛ Weil B؛ Wellenreuther R؛ وآخرون (2001)، "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs"، Genome Res.، 11 (3): 422–35، doi:10.1101/gr.GR1547R، PMC 311072، PMID 11230166.
- Simpson JC؛ Wellenreuther R؛ Poustka A؛ وآخرون (2001)، "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing"، EMBO Rep.، 1 (3): 287–92، doi:10.1093/embo-reports/kvd058، PMC 1083732، PMID 11256614.
- Pröls F؛ Mayer MP؛ Renner O؛ وآخرون (2001)، "Upregulation of the cochaperone Mdg1 in endothelial cells is induced by stress and during in vitro angiogenesis"، Exp. Cell Res.، 269 (1): 42–53، doi:10.1006/excr.2001.5294، PMID 11525638.
- "Identification and characterization of a novel endoplasmic reticulum (ER) DnaJ homologue, which stimulates ATPase activity of BiP in vitro and is induced by ER stress"، J. Biol. Chem.، 277 (18): 15947–56، 2002، doi:10.1074/jbc.M112214200، PMID 11836248.
- Strausberg RL؛ Feingold EA؛ Grouse LH؛ وآخرون (2003)، "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- Scherer SW؛ Cheung J؛ MacDonald JR؛ وآخرون (2003)، "Human Chromosome 7: DNA Sequence and Biology"، Science، 300 (5620): 767–72، doi:10.1126/science.1083423، PMC 2882961، PMID 12690205.
- Clark HF؛ Gurney AL؛ Abaya E؛ وآخرون (2003)، "The Secreted Protein Discovery Initiative (SPDI), a Large-Scale Effort to Identify Novel Human Secreted and Transmembrane Proteins: A Bioinformatics Assessment"، Genome Res.، 13 (10): 2265–70، doi:10.1101/gr.1293003، PMC 403697، PMID 12975309.
- Berger BJ؛ Müller TS؛ Buschmann IR؛ وآخرون (2003)، "High levels of the molecular chaperone Mdg1/ERdj4 reflect the activation state of endothelial cells"، Exp. Cell Res.، 290 (1): 82–92، doi:10.1016/S0014-4827(03)00316-1، PMID 14516790.
- Ota T؛ Suzuki Y؛ Nishikawa T؛ وآخرون (2004)، "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، doi:10.1038/ng1285، PMID 14702039.
- "The WW Domain-Containing Proteins Interact with the Early Spliceosome and Participate in Pre-mRNA Splicing In Vivo"، Mol. Cell. Biol.، 24 (20): 9176–85، 2004، doi:10.1128/MCB.24.20.9176-9185.2004، PMC 517884، PMID 15456888.
- Gerhard DS؛ Wagner L؛ Feingold EA؛ وآخرون (2004)، "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)"، Genome Res.، 14 (10B): 2121–7، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- Stelzl U؛ Worm U؛ Lalowski M؛ وآخرون (2005)، "A human protein-protein interaction network: a resource for annotating the proteome"، Cell، 122 (6): 957–68، doi:10.1016/j.cell.2005.08.029، PMID 16169070.
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