ZIC2
ZIC2 (Zic family member 2) هوَ بروتين يُشَفر بواسطة جين ZIC2 في الإنسان.[1][2][3]
المراجع
- "Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired"، Nat Genet، 20 (2): 180–3، 1998، doi:10.1038/2484، PMID 9771712.
- "Entrez Gene: ZIC2 Zic family member 2 (odd-paired homolog, Drosophila)"، مؤرشف من الأصل في 5 ديسمبر 2010.
- "Zinc finger of the cerebellum (Zic): Transcription factors and co-factors"، Int J Biochem Cell Biol، 44 (11): 2065–8، نوفمبر 2012، doi:10.1016/j.biocel.2012.08.012، PMID 22964024.
قراءة متعمقة
- "The ZIC gene family encodes multi-functional proteins essential for patterning and morphogenesis."، Cell Mol Life Sci، 70 (20): 3791–811، 2013، doi:10.1007/s00018-013-1285-5، PMID 23443491.
- "Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature."، Am. J. Med. Genet.، 45 (1): 52–9، 1993، doi:10.1002/ajmg.1320450115، PMID 8418661.
- "Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination"، Hum. Mol. Genet.، 10 (8): 791–6، 2001، doi:10.1093/hmg/10.8.791، PMID 11285244.
- "Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations"، Hum. Mutat.، 24 (1): 43–51، 2004، doi:10.1002/humu.20056، PMID 15221788.
- "In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation"، Hum. Mol. Genet.، 14 (3): 411–20، 2005، doi:10.1093/hmg/ddi037، PMID 15590697.
- "ZIC2-dependent transcriptional regulation is mediated by DNA-dependent protein kinase, poly(ADP-ribose) polymerase, and RNA helicase A"، J. Biol. Chem.، 282 (13): 9983–95، 2007، doi:10.1074/jbc.M610821200، PMID 17251188.
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة طب
- بوابة الكيمياء الحيوية
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