Sobe T - Search Results

1

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Sobe T, Vreugde S, Shahin H, Berlin M, Davis N, Kanaan M, Yaron Y, Orr-Urtreger A, Frydman M, Shohat M, Avraham KB. Sobe T, et al. Hum Genet. 2000 Jan;106(1):50-7. doi: 10.1007/s004390051009. Hum Genet. 2000. PMID: 10982182

2

Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.

Shahin H, Walsh T, Sobe T, Lynch E, King MC, Avraham KB, Kanaan M. Shahin H, et al. Among authors: sobe t. Hum Genet. 2002 Mar;110(3):284-9. doi: 10.1007/s00439-001-0674-2. Epub 2002 Feb 8. Hum Genet. 2002. PMID: 11935342

3

Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.

Shahin H, Walsh T, Sobe T, Abu Sa'ed J, Abu Rayan A, Lynch ED, Lee MK, Avraham KB, King MC, Kanaan M. Shahin H, et al. Among authors: sobe t. Am J Hum Genet. 2006 Jan;78(1):144-52. doi: 10.1086/499495. Epub 2005 Nov 21. Am J Hum Genet. 2006. PMID: 16385458 Free PMC article.

4

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice.

Avraham KB, Hasson T, Sobe T, Balsara B, Testa JR, Skvorak AB, Morton CC, Copeland NG, Jenkins NA. Avraham KB, et al. Among authors: sobe t. Hum Mol Genet. 1997 Aug;6(8):1225-31. doi: 10.1093/hmg/6.8.1225. Hum Mol Genet. 1997. PMID: 9259267

5

High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim.

Sobe T, Erlich P, Berry A, Korostichevsky M, Vreugde S, Avraham KB, Bonné-Tamir B, Shohat M. Sobe T, et al. Am J Med Genet. 1999 Oct 29;86(5):499-500. Am J Med Genet. 1999. PMID: 10508996 No abstract available.

6

Genomic structure of the human unconventional myosin VI gene.

Ahituv N, Sobe T, Robertson NG, Morton CC, Taggart RT, Avraham KB. Ahituv N, et al. Among authors: sobe t. Gene. 2000 Dec 31;261(2):269-75. doi: 10.1016/s0378-1119(00)00535-7. Gene. 2000. PMID: 11167014

7

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.

Melchionda S, Ahituv N, Bisceglia L, Sobe T, Glaser F, Rabionet R, Arbones ML, Notarangelo A, Di Iorio E, Carella M, Zelante L, Estivill X, Avraham KB, Gasparini P. Melchionda S, et al. Among authors: sobe t. Am J Hum Genet. 2001 Sep;69(3):635-40. doi: 10.1086/323156. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468689 Free PMC article.

8

Targeted disruption of the mouse Caspase 8 gene ablates cell death induction by the TNF receptors, Fas/Apo1, and DR3 and is lethal prenatally.

Varfolomeev EE, Schuchmann M, Luria V, Chiannilkulchai N, Beckmann JS, Mett IL, Rebrikov D, Brodianski VM, Kemper OC, Kollet O, Lapidot T, Soffer D, Sobe T, Avraham KB, Goncharov T, Holtmann H, Lonai P, Wallach D. Varfolomeev EE, et al. Among authors: sobe t. Immunity. 1998 Aug;9(2):267-76. doi: 10.1016/s1074-7613(00)80609-3. Immunity. 1998. PMID: 9729047 Free article.

9

Role of myosin VI in the differentiation of cochlear hair cells.

Self T, Sobe T, Copeland NG, Jenkins NA, Avraham KB, Steel KP. Self T, et al. Among authors: sobe t. Dev Biol. 1999 Oct 15;214(2):331-41. doi: 10.1006/dbio.1999.9424. Dev Biol. 1999. PMID: 10525338 Free article.

10

Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life.

Slor H, Batko S, Khan SG, Sobe T, Emmert S, Khadavi A, Frumkin A, Busch DB, Albert RB, Kraemer KH. Slor H, et al. Among authors: sobe t. J Invest Dermatol. 2000 Dec;115(6):974-80. doi: 10.1046/j.1523-1747.2000.00190.x. J Invest Dermatol. 2000. PMID: 11121128 Free article.

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