DFNA5
DFNA5 (Gasdermin E) هوَ بروتين يُشَفر بواسطة جين DFNA5 في الإنسان.[1][2][3]
المراجع
- "Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15"، Hum Mol Genet، 4 (11): 2159–63، مارس 1996، doi:10.1093/hmg/4.11.2159، PMID 8589696.
- "Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea"، Eur J Hum Genet، 5 (6): 397–405، مارس 1998، PMID 9450185.
- "Entrez Gene: DFNA5 deafness, autosomal dominant 5"، مؤرشف من الأصل في 7 مارس 2010.
قراءة متعمقة
- "A "double adaptor" method for improved shotgun library construction"، Anal. Biochem.، 236 (1): 107–13، 1996، doi:10.1006/abio.1996.0138، PMID 8619474.
- "Large-scale concatenation cDNA sequencing"، Genome Res.، 7 (4): 353–8، 1997، doi:10.1101/gr.7.4.353، PMC 139146، PMID 9110174.
- "Characterization of a gene that is inversely correlated with estrogen receptor expression (ICERE-1) in breast carcinomas"، Eur. J. Biochem.، 252 (1): 169–77، 1998، doi:10.1046/j.1432-1327.1998.2520169.x، PMID 9523727.
- "Nonsyndromic hearing impairment is associated with a mutation in DFNA5"، Nat. Genet.، 20 (2): 194–7، 1998، doi:10.1038/2503، PMID 9771715.
- "Identification of differentially expressed genes in human melanoma cells with acquired resistance to various antineoplastic drugs"، Int. J. Cancer، 88 (4): 535–46، 2000، doi:10.1002/1097-0215(20001115)88:4<535::AID-IJC4>3.0.CO;2-V، PMID 11058868.
- "Is DFNA5 a susceptibility gene for age-related hearing impairment?"، Eur. J. Hum. Genet.، 10 (12): 883–6، 2003، doi:10.1038/sj.ejhg.5200878، PMID 12461698.
- "A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment"، Biochim. Biophys. Acta، 1638 (2): 179–86، 2003، doi:10.1016/s0925-4439(03)00083-8، PMID 12853124.
- "A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family"، Genomics، 82 (5): 575–9، 2004، doi:10.1016/S0888-7543(03)00175-7، PMID 14559215.
- "A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation"، Audiol. Neurootol.، 9 (1): 34–46، 2004، doi:10.1159/000074185، PMID 14676472.
- "The potential role of DFNA5, a hearing impairment gene, in p53-mediated cellular response to DNA damage"، J. Hum. Genet.، 51 (8): 652–64، 2006، doi:10.1007/s10038-006-0004-6، PMID 16897187.
- "A novel DFNA5 mutation does not cause hearing loss in an Iranian family"، J. Hum. Genet.، 52 (6): 549–52، 2007، doi:10.1007/s10038-007-0137-2، PMID 17427029.
بوابة الكيمياء الحيوية
بوابة طب
بوابة علم الأحياء الخلوي والجزيئي
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