CENTA2
CENTA2 (ArfGAP with dual PH domains 2) هوَ بروتين يُشَفر بواسطة جين CENTA2 في الإنسان.[1]
المراجع
- "Entrez Gene: CENTA2 centaurin, alpha 2"، مؤرشف من الأصل في 05 ديسمبر 2010.
قراءة متعمقة
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides."، Gene، 138 (1–2): 171–4، 1994، doi:10.1016/0378-1119(94)90802-8، PMID 8125298.
- Suzuki Y؛ Yoshitomo-Nakagawa K؛ Maruyama K؛ وآخرون (1997)، "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library"، Gene، 200 (1–2): 149–56، doi:10.1016/S0378-1119(97)00411-3، PMID 9373149.
- Jenne DE؛ Tinschert S؛ Stegmann E؛ وآخرون (2000)، "A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions"، Genomics، 66 (1): 93–7، doi:10.1006/geno.2000.6179، PMID 10843809.
- Whitley P؛ Gibbard AM؛ Koumanov F؛ وآخرون (2003)، "Identification of centaurin-alpha2: a phosphatidylinositide-binding protein present in fat, heart and skeletal muscle"، Eur. J. Cell Biol.، 81 (4): 222–30، doi:10.1078/0171-9335-00242، PMID 12018390.
- 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.
- "Identification of gene structure and subcellular localization of human centaurin alpha 2, and p42IP4, a family of two highly homologous, Ins 1,3,4,5-P4-/PtdIns 3,4,5-P3-binding, adapter proteins"، J. Neurochem.، 88 (2): 326–36، 2004، doi:10.1046/j.1471-4159.2003.02143.x، PMID 14690521.
- 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.
- Venturin M؛ Bentivegna A؛ Moroni R؛ وآخرون (2005)، "Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval"، Ann. Hum. Genet.، 69 (Pt 5): 508–16، doi:10.1111/j.1529-8817.2005.00203.x، PMID 16138909.
- Douglas J؛ Cilliers D؛ Coleman K؛ وآخرون (2007)، "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth"، Nat. Genet.، 39 (8): 963–5، doi:10.1038/ng2083، PMID 17632510.
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة الكيمياء الحيوية
- بوابة طب
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