Resultados de búsqueda - Edna Ben‐Asher

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  1. 1
    Transcription of minute virus of mice, an autonomous parvovirus, may be regulated by attenuation

    Transcription of minute virus of mice, an autonomous parvovirus, may be regulated by attenuation por Edna Ben‐Asher, Yosef Aloni

    Publicado 1984
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  2. 2
    Mechanisms for Evolving Hypervariability: The Case of Conopeptides

    Mechanisms for Evolving Hypervariability: The Case of Conopeptides por Silvestro G. Conticello, Yoav Gilad, Nili Avidan, Edna Ben‐Asher, Zehava Levy, Mike Fainzilber

    Publicado 2001
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  3. 3
    DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population

    DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population por Anna Alkelai, Sara Lupoli, Lior Greenbaum, Yoav Kohn, Kyra Kanyas-Sarner, Edna Ben‐Asher, Doron Lancet, Fabìo Macciardi, Bernard Lerer

    Publicado 2011
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  4. 4
    Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample

    Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample por Anna Alkelai, Lior Greenbaum, Sara Lupoli, Yoav Kohn, Kyra Sarner-Kanyas, Edna Ben‐Asher, Doron Lancet, Fabìo Macciardi, Bernard Lerer

    Publicado 2012
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  5. 5
    Personal receptor repertoires: olfaction as a model

    Personal receptor repertoires: olfaction as a model por Tsviya Olender, Sebastian M. Waszak, Maya Viavant, Miriam Khen, Edna Ben‐Asher, Alejandro Reyes, Noam Nativ, Charles J. Wysocki, Dongliang Ge, Doron Lancet

    Publicado 2012
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  6. 6
    Mucolipidosis type IV: NovelMCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population

    Mucolipidosis type IV: NovelMCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population por Ruth Bargal, Nili Avidan, Tzvia Olender, Edna Ben Asher, Marcia Zeigler, Annick Raas‐Rothschild, Ayala Frumkin, Omer Ben-Yoseph, Yechiel Friedlender, Doron Lancet, Gideon Bach

    Publicado 2001
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  7. 7
    A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel

    A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from... por Hadas Lahat, Elon Pras, Tsviya Olender, Nili Avidan, Edna Ben‐Asher, Orna Man, Etgar Levy‐Nissenbaum, Asad Khoury, Avraham Lorber, Boleslaw Goldman, Doron Lancet, Michael Eldar

    Publicado 2001
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  8. 8
    General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations

    General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations por Ifat Keydar, Edna Ben‐Asher, Ester Feldmesser, Noam Nativ, Arisa Oshimoto, Diego Restrepo, Hiroaki Matsunami, Ming‐Shan Chien, Jayant M. Pinto, Yoav Gilad, Tsviya Olender, Doron Lancet

    Publicado 2012
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  9. 9
    AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia

    AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia por Daniela Amann‐Zalcenstein, Nili Avidan, Kyra Kanyas, Richard P. Ebstein, Yoav Kohn, Adnan Hamdan, Edna Ben‐Asher, Osnat Karni, Muhammed Mujaheed, Ronnen H. Segman, Wolfgang Maier, Fabìo Macciardi, J. Beckmann, Doron Lancet, Bernard Lerer

    Publicado 2006
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  10. 10
    Haplotype structure and selection of the MDM2 oncogene in humans

    Haplotype structure and selection of the MDM2 oncogene in humans por Gurinder S. Atwal, Gareth L. Bond, Sally Metsuyanim, Moshe Z. Papa, Eitan Friedman, Tal Distelman-Menachem, Edna Ben Asher, Doron Lancet, David A. Ross, John J. Sninsky, Tomas J. White, Arnold J. Levine, Ronit I. Yarden

    Publicado 2007
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  11. 11
    Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene

    Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene por Dan Vodo, Ofer Sarig, Shamir Geller, Edna Ben‐Asher, Tsviya Olender, Ron Bochner, Ilan Goldberg, Judith Nosgorodsky, Anna Alkelai, Pavel Tatarskyy, A. Peled, Sharon Baum, Aviv Barzilai, Saleh Ibrahim, Detlef Zillikens, Doron Lancet, Eli Sprecher

    Publicado 2016
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  12. 12
    CATSPER2, a human autosomal nonsyndromic male infertility gene

    CATSPER2, a human autosomal nonsyndromic male infertility gene por Nili Avidan, Hannah Tamary, Orly Dgany, D Cattan, Alexandre Pariente, Michel Thulliez, N. Borot, Lucien Moati, Alain Barthelme, Lea Shalmon, Tatyana Krasnov, Edna Ben‐Asher, Tsvyia Olender, Miriam Khen, Issac Yaniv, Rina Zaizov, Hanna Shalev, J. Delaunay, Marc Fellous, Doron Lancet, J. Beckmann

    Publicado 2003
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  13. 13
    USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

    USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses por Avital Adato, Sarah Vreugde, Tarja Joensuu, Nili Avidan, Riikka H. Hämäläinen, Olga Belenkiy, Tsviya Olender, Batsheva Bonné‐Tamir, Edna Ben‐Asher, Carmen Espinós, José M. Millán, Anna‐Elina Lehesjoki, John G. Flannery, Karen B. Avraham, Shmuel Pietrokovski, Eeva-Marja Sankila, J. Beckmann, Doron Lancet

    Publicado 2002
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  14. 14
    Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis

    Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis por Danit Oz-Levi, Bruria Ben‐Zeev, Elizabeth K. Ruzzo, Yuki Hitomi, Amir Gelman, Kimberly Pelak, Yair Anikster, Haike Reznik‐Wolf, Ifat Bar-Joseph, Tsviya Olender, Anna Alkelai, Meira Weiss, Edna Ben‐Asher, Dongliang Ge, Kevin V. Shianna, Zvulun Elazar, David B. Goldstein, Elon Pras, Doron Lancet

    Publicado 2012
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  15. 15
    Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

    Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1 por Orly Dgany, Nili Avidan, J. Delaunay, Tatyana Krasnov, Lea Shalmon, Hanna Shalev, Tal Eidelitz‐Markus, Joseph Kapelushnik, D Cattan, Alexandre Pariente, Michel Tulliez, Aurore Crétien, Pierre–Olivier Schischmanoff, Achille Iolascon, Eithan Fibach, Ariel Koren, Jochen Rößler, Martine Le Merrer, Isaac Yaniv, Rina Zaizov, Edna Ben‐Asher, Tsvyia Olender, Doron Lancet, J. Beckmann, Hannah Tamary

    Publicado 2002
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  16. 16
    Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy

    Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy por Elizabeth K. Ruzzo, José‐Mario Capo‐Chichi, Bruria Ben‐Zeev, David Chitayat, Hanqian Mao, Andrea L. Pappas, Yuki Hitomi, Yifan Lu, Xiaodi Yao, Fadi F. Hamdan, Kimberly Pelak, Haike Reznik‐Wolf, Ifat Bar-Joseph, Danit Oz-Levi, Dorit Lev, Tally Lerman‐Sagie, Esther Leshinsky‐Silver, Yair Anikster, Edna Ben‐Asher, Tsviya Olender, Laurence Colleaux, Jean‐Claude Décarie, Susan Blasér, Brenda Banwell, Rasesh B. Joshi, Xiao‐Ping He, Lysanne Patry, Rachel Silver, Sylvia Dobrzeniecka, Mohammad S. Islam, Abul Hasnat, Mark E. Samuels, Dipendra K. Aryal, Ramona M. Rodriguiz, Yong‐hui Jiang, William C. Wetsel, James O McNamara, Guy A. Rouleau, Debra L. Silver, Doron Lancet, Elon Pras, Grant A. Mitchell, Jacques L. Michaud, David B. Goldstein

    Publicado 2013
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