检索结果 - Tama Sobe
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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 由 Hashem Shahin, Tom Walsh, Tama Sobe, Judeh Abu Sa’ed, Amal Rayan, Eric D. Lynch, Ming K. Lee, Karen B. Avraham, Mary‐Claire King, Moien Kanaan
出版 2005Artigo -
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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 由 Salvatore Melchionda, Nadav Ahituv, Luigi Bisceglia, Tama Sobe, Fabian Glaser, Raquel Rabionet, María L. Arbonés, Angelo Notarangelo, Enzo Di Iorio, Massimo Carella, Leopoldo Zelante, Xavier Estivill, Karen B. Avraham, Paolo Gasparini
出版 2001Artigo -
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Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally 由 Eugene Varfolomeev, Marcus Schuchmann, Victor Luria, Nuchanard Chiannilkulchai, J. Beckmann, Igor Mett, Denis Rebrikov, Vadim M Brodianski, Oliver Kemper, Órit Kollet, Tsvee Lapidot, Dror Soffer, Tama Sobe, Karen B. Avraham, Tanya Goncharov, Helmut Holtmann, Peter Lonai, David Wallach
出版 1998Artigo
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Biology
Gene
Genetics
Audiology
Cell biology
Hearing loss
Medicine
Actin
Anatomy
Apoptosis
Caspase
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Fas receptor
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Gene isoform
Gene targeting
Haematopoiesis
Hair cell
Immunology
Inner ear
Kinocilium
Molecular biology
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Mutation
Myosin
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Programmed cell death
Receptor