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Results:
1-7
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Results: 7
Authors:
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
Citation: S. Melchionda et al., MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss, AM J HU GEN, 69(3), 2001, pp. 635-640
Authors:
Ahituv, N
Sobe, T
Robertson, NG
Morton, CC
Taggart, RT
Avraham, KB
Citation: N. Ahituv et al., Genomic structure of the human unconventional myosin VI gene, GENE, 261(2), 2000, pp. 269-275
Authors:
Sobe, T
Vreugde, S
Shahin, H
Berlin, M
Davis, N
Kanaan, M
Yaron, Y
Orr-Urtreger, A
Frydman, M
Shohat, M
Avraham, KB
Citation: T. Sobe et al., The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population, HUM GENET, 106(1), 2000, pp. 50-57
Authors:
Slor, H
Batko, S
Khan, SG
Sobe, T
Emmert, S
Khadavi, A
Frumkin, A
Busch, DB
Albert, RB
Kraemer, KH
Citation: H. Slor et al., Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: Sun protection prolongs life, J INVES DER, 115(6), 2000, pp. 974-980
Authors:
Ronen, D
Altstock, RT
Firon, M
Mittelman, L
Sobe, T
Resau, JH
Woude, GFV
Tsarfaty, I
Citation: D. Ronen et al., Met-HGF/SF mediates growth arrest and differentiation in T47D breast cancer cells, CELL GROWTH, 10(2), 1999, pp. 131-140
Authors:
Sobe, T
Erlich, P
Berry, A
Korostichevsky, M
Vreugde, S
Avraham, KB
Bonne-Tanir, B
Shohat, M
Citation: T. Sobe et al., High frequency of the deafness-associated 167delT mutation in the connexin26 (GJB2) gene in Israeli Ashkenazim, AM J MED G, 86(5), 1999, pp. 499-500
Authors:
Self, T
Sobe, T
Copeland, NG
Jenkins, NA
Avraham, KB
Steel, KP
Citation: T. Self et al., Role of myosin VI in the differentiation of cochlear hair cells, DEVELOP BIO, 214(2), 1999, pp. 331-341
Risultati:
1-7
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