Resultats de la cerca - Ephrat Levy‐Lahad

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  1. 1
    Cancer risks among BRCA1 and BRCA2 mutation carriers

    Cancer risks among BRCA1 and BRCA2 mutation carriers per Ephrat Levy‐Lahad, Eitan Friedman

    Publicat 2007
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  2. 2
    Precision Medicine Meets Public Health: Population Screening for BRCA1 and BRCA2

    Precision Medicine Meets Public Health: Population Screening for BRCA1 and BRCA2 per Ephrat Levy‐Lahad, Amnon Lahad, Mary‐Claire King

    Publicat 2014
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  3. 3
    Dr. Segel and colleagues reply

    Dr. Segel and colleagues reply per Reeval Segel, Mary‐Claire King, Ephrat Levy‐Lahad

    Publicat 2014
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  4. 4
    Population Screening for Inherited Predisposition to Breast and Ovarian Cancer

    Population Screening for Inherited Predisposition to Breast and Ovarian Cancer per Ranjit Manchanda, Sari Lieberman, Faiza Gaba, Amnon Lahad, Ephrat Levy‐Lahad

    Publicat 2020
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  5. 5
    Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

    Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia per Michael Kaplan, Paul Renbaum, Ephrat Levy‐Lahad, Cathy Hammerman, Amnon Lahad, Ernest Beutler

    Publicat 1997
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  6. 6
    BRCA Mutation Carriers Do Not Have Compromised Ovarian Reserve

    BRCA Mutation Carriers Do Not Have Compromised Ovarian Reserve per Rachel Michaelson‐Cohen, Pnina Mor, Naama Srebnik, Uziel Beller, Ephrat Levy‐Lahad, Talia Eldar‐Geva

    Publicat 2014
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  7. 7
    VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle

    VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle per Lara Cantarero, Marta Sanz-García, Hadar Vinograd-Byk, Paul Renbaum, Ephrat Levy‐Lahad, Pedro A. Lazo

    Publicat 2015
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  8. 8
    Familial communication and cascade testing among relatives of BRCA population screening participants

    Familial communication and cascade testing among relatives of BRCA population screening participants per Sari Lieberman, Amnon Lahad, Ariela Tomer, Sivan Koka, Malka BenUziyahu, Aviad E. Raz, Ephrat Levy‐Lahad

    Publicat 2018
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  9. 9
    Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene

    Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene per Paul Renbaum, Efrat Kellerman, Ranit Jaron, Dan Geiger, Reeval Segel, Ming Lee, Mary‐Claire King, Ephrat Levy‐Lahad

    Publicat 2009
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  10. 10
    Neonatal outcome after preimplantation genetic diagnosis

    Neonatal outcome after preimplantation genetic diagnosis per Talia Eldar‐Geva, Naama Srebnik, Gheona Altarescu, Irit Varshaver, Baruch Brooks, Ephrat Levy‐Lahad, Ruben Bromiker, Michael S. Schimmel

    Publicat 2014
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  11. 11
    Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome

    Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome per Sarah B. Pierce, Ksenija Geršak, Rachel Michaelson‐Cohen, Tom Walsh, Ming K. Lee, Daniel Malach, Rachel E. Klevit, Mary‐Claire King, Ephrat Levy‐Lahad

    Publicat 2013
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  12. 12
    Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood

    Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood per Gidon Toperoff, Dvir Aran, Jeremy D. Kark, Michael Rosenberg, Tatyana Dubnikov, Batel Nissan, Julio Wainstein, Yechiel Friedlander, Ephrat Levy‐Lahad, Benjamin Gläser, Asaf Hellman

    Publicat 2011
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  13. 13
    A single nucleotide polymorphism in the <i>RAD51</i> gene modifies cancer risk in <i>BRCA2</i> but not <i>BRCA1</i> carriers

    A single nucleotide polymorphism in the <i>RAD51</i> gene modifies cancer risk in <i>BRCA2</i> but not <i>BRCA1</i> carriers per Ephrat Levy‐Lahad, Amnon Lahad, Shlomit Eisenberg, Efrat Dagan, Tamar Paperna, L Kasinetz, Raphael Catane, Bella Kaufman, Uziel Beller, Paul Renbaum, Ruth Gershoni‐Baruch

    Publicat 2001
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  14. 14
    FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells

    FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells per Michal Avitzour, Hagar Mor‐Shaked, Shira Yanovsky‐Dagan, Shira Aharoni, Gheona Altarescu, Paul Renbaum, Talia Eldar‐Geva, Oshrat Schonberger, Ephrat Levy‐Lahad, Silvina Epsztejn‐Litman, Rachel Eiges

    Publicat 2014
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  15. 15
    Mutations in the DBP-Deficiency Protein HSD17B4 Cause Ovarian Dysgenesis, Hearing Loss, and Ataxia of Perrault Syndrome

    Mutations in the DBP-Deficiency Protein HSD17B4 Cause Ovarian Dysgenesis, Hearing Loss, and Ataxia of Perrault Syndrome per Sarah B. Pierce, Tom Walsh, Karen M. Chisholm, Ming K. Lee, Anne Thornton, Agata Fiumara, John M. Opitz, Ephrat Levy‐Lahad, Rachel E. Klevit, Mary‐Claire King

    Publicat 2010
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  16. 16
    Cost-effectiveness of population based BRCA testing with varying Ashkenazi Jewish ancestry

    Cost-effectiveness of population based BRCA testing with varying Ashkenazi Jewish ancestry per Ranjit Manchanda, Shreeya Patel, Antonis C. Antoniou, Ephrat Levy‐Lahad, Clare Turnbull, D. Gareth Evans, John L. Hopper, Robert J. MacInnis, Usha Menon, Ian Jacobs, Rosa Legood

    Publicat 2017
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  17. 17
    The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects

    The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects per Hila Fridman, Helger G. Yntema, Reedik Mägi, Reidar Andreson, Andres Metspalu, Massimo Mezzavilla, Chris Tyler‐Smith, Yali Xue, Shai Carmi, Ephrat Levy‐Lahad, Christian Gilissen, Han G. Brunner

    Publicat 2021
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  18. 18
    Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

    Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells per Shira Yanovsky‐Dagan, Michal Avitzour, Gheona Altarescu, Paul Renbaum, Talia Eldar‐Geva, Oshrat Schonberger, Stella Mitrani‐Rosenbaum, Ephrat Levy‐Lahad, Ramon Y. Birnbaum, Lior Gepstein, Silvina Epsztejn‐Litman, Rachel Eiges

    Publicat 2015
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  19. 19
    XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

    XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription per David Zangen, Yotam Kaufman, Sharon Zeligson, Shira Perlberg, Hila Fridman, Moien Kanaan, Maha Abdulhadi‐Atwan, Abdulsalam Abu‐Libdeh, Ayal B. Gussow, Irit Kisslov, Liran Carmel, Paul Renbaum, Ephrat Levy‐Lahad

    Publicat 2011
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  20. 20
    Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population

    Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population per Avraham Shaag, Tom Walsh, Paul Renbaum, Tomas Kirchhoff, Khédoudja Nafa, Stacey Shiovitz, Jessica B. Mandell, Piri Welcsh, Ming K. Lee, Nathan A. Ellis, Kenneth Offit, Ephrat Levy‐Lahad, Mary‐Claire King

    Publicat 2005
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