Výsledky vyhledávání - Edna Ben‐Asher
- Zobrazuji výsledky 1 - 16 z 16
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Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample Autor Anna Alkelai, Lior Greenbaum, Sara Lupoli, Yoav Kohn, Kyra Sarner-Kanyas, Edna Ben‐Asher, Doron Lancet, Fabìo Macciardi, Bernard Lerer
Vydáno 2012Artigo -
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Mucolipidosis type IV: NovelMCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population Autor 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
Vydáno 2001Artigo -
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A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from... Autor 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
Vydáno 2001Artigo -
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General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations Autor 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
Vydáno 2012Artigo -
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AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia Autor 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
Vydáno 2006Artigo -
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Haplotype structure and selection of the MDM2 oncogene in humans Autor 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
Vydáno 2007Artigo -
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Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene Autor 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
Vydáno 2016Artigo -
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CATSPER2, a human autosomal nonsyndromic male infertility gene Autor 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
Vydáno 2003Artigo -
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USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses Autor 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
Vydáno 2002Artigo -
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Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis Autor 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
Vydáno 2012Artigo -
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Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1 Autor 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
Vydáno 2002Artigo -
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Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy Autor 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
Vydáno 2013Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Mutation
Receptor
Genotype
Population
Single-nucleotide polymorphism
Allele
Computational biology
Genome
Haplotype
Missense mutation
Phenotype
Candidate gene
Cell biology
Demography
Environmental health
Evolutionary biology
Gene expression
Genetic association
Genome-wide association study
Internal medicine
Locus (genetics)
Neuroscience
Olfactory receptor
Pseudogene
Psychiatry
SNP