Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally by Varfolomeev, Eugene E, Schuchmann, Marcus, Luria, Victor, Chiannilkulchai, Nuchanard, Beckmann, Jacques S, Mett, Igor L, Rebrikov, Denis, Brodianski, Vadim M, Kemper, Oliver C, Kollet, Orit, Lapidot, Tsvee, Soffer, Dror, Sobe, Tama, Avraham, Karen B, Goncharov, Tanya, Holtmann, Helmut, Lonai, Peter, Wallach, David

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MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss by Melchionda, Salvatore, Ahituv, Nadav, Bisceglia, Luigi, Sobe, Tama, Glaser, Fabian, Rabionet, Raquel, Arbones, Maria Lourdes, Notarangelo, Angelo, Di Iorio, Enzo, Carella, Massimo, Zelante, Leopoldo, Estivill, Xavier, Avraham, Karen B., Gasparini, Paolo

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Role of Myosin VI in the Differentiation of Cochlear Hair Cells by Self, Tim, Sobe, Tama, Copeland, Neal G., Jenkins, Nancy A., Avraham, Karen B., Steel, Karen P.

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Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss by Shahin, Hashem, Walsh, Tom, Sobe, Tama, Abu Sa’ed, Judeh, Abu Rayan, Amal, Lynch, Eric D., Lee, Ming K., Avraham, Karen B., King, Mary-Claire, Kanaan, Moein

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Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East by SHAHIN, Hashem, WALSH, Tom, SOBE, Tama, LYNCH, Eric, KING, Mary-Claire, AVRAHAM, Karen B, KANAAN, Moien

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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population by SOBE, T, VREUGDE, S, AVRAHAM, K. B, SHAHIN, H, BERLIN, M, DAVIS, N, KANAAN, M, YARON, Y, ORR-URTREGER, A, FRYDMAN, M, SHOHAT, M

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Characterization of Unconventional MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell's Waltzer Mice by Avraham, Karen B., Hasson, Tama, Sobe, Tama, Balsara, Binaifer, Testa, Joseph R., Skvorak, Anne B., Morton, Cynthia C., Copeland, Neal G., Jenkins, Nancy A.

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Genomic structure of the human unconventional myosin VI gene by Ahituv, Nadav, Sobe, Tama, Robertson, Nahid G, Morton, Cynthia C, Taggart, R.Thomas, Avraham, Karen B

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GAP JUNCTION PROTEIN CONNEXIN 26 MUTATIONS IN THE PRELINGUAL DEAF PALESTINIAN POPULATION by Kanaan, Moien, Shahin, Hashim, Sobe, Tama, Avraham, Karen

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THE GENETICS OF HEARING LOSS IN THE PALESTINIAN POPULATION by Shahin, Hashem, Sobe, Tama, Morrow, J., Lynch, Eric, King, Mary-Claire, Avraham, Karen, Kanaan, Moien

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High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim by Sobe, Tama, Erlich, Porat, Berry, Asher, Korostichevsky, Michael, Vreugde, Sarah, Avraham, Karen B., Bonné-Tamir, Batsheva, Shohat, Mordechai

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