CEMIP
CEMIP (Cell migration inducing hyaluronidase 1) هوَ بروتين يُشَفر بواسطة جين CEMIP في الإنسان.[1][2][3][4][5]
الوظيفة
المراجع
- Zhang, Yongsheng؛ Jia, Shuqin؛ Jiang, Wen (20 فبراير 2014)، "KIAA1199 and its biological role in human cancer and cancer cells (Review)"، Oncology Reports، doi:10.3892/or.2014.3038.
- Yoshida, H.؛ Nagaoka, A.؛ Kusaka-Kikushima, A.؛ Tobiishi, M.؛ Kawabata, K.؛ Sayo, T.؛ Sakai, S.؛ Sugiyama, Y.؛ Enomoto, H.؛ Okada, Y.؛ Inoue, S. (18 مارس 2013)، "KIAA1199, a deafness gene of unknown function, is a new hyaluronan binding protein involved in hyaluronan depolymerization"، Proceedings of the National Academy of Sciences، 110 (14): 5612–5617، doi:10.1073/pnas.1215432110، PMC 3619336، PMID 23509262.
- Yoshida, Hiroyuki؛ Nagaoka, Aya؛ Nakamura, Sachiko؛ Sugiyama, Yoshinori؛ Okada, Yasunori؛ Inoue, Shintaro (17 أغسطس 2013)، "Murine homologue of the human KIAA1199 is implicated in hyaluronan binding and depolymerization"، FEBS Open Bio، 3 (1): 352–356، doi:10.1016/j.fob.2013.08.003.
- "Entrez Gene: KIAA1199 KIAA1199"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss"، J Hum Genet، 48 (11): 564–70، نوفمبر 2003، doi:10.1007/s10038-003-0079-2، PMID 14577002.
قراءة متعمقة
- "Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro."، DNA Res.، 6 (5): 337–45، 2000، doi:10.1093/dnares/6.5.337، PMID 10574462.
- "Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis."، Genomics، 72 (1): 88–98، 2001، doi:10.1006/geno.2000.6466، PMID 11247670.
- "Protein–Protein Interactions Between Large Proteins: Two-Hybrid Screening Using a Functionally Classified Library Composed of Long cDNAs"، Genome Res.، 12 (11): 1773–84، 2003، doi:10.1101/gr.406902، PMC 187542، PMID 12421765.
- "Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues"، Am. J. Hum. Genet.، 72 (1): 73–82، 2003، doi:10.1086/345398، PMC 420014، PMID 12471561.
- "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، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)"، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "GG: a domain involved in phage LTF apparatus and implicated in human MEB and non-syndromic hearing loss diseases"، FEBS Lett.، 580 (2): 581–4، 2006، doi:10.1016/j.febslet.2005.12.076، PMID 16406369.
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