Výsledky vyhledávání - "Efrat Kellerman"

Akademický článek

Frequency of canine nt230(del4) MDR1 mutation in prone pure breeds, their crosses and mongrels in Israel - insights from a worldwide comparative perspective.

Autor: Yaron Dekel, Yossy Machluf, Aviad Stoler, Arava Aderet, Daniel Baumel, Efrat Kellerman, Yoram Plotsky, Oshrat Noked Partouche, Gal Elhalal, Izhar Ben-Shlomo, Dani Bercovich

Publikováno v: BMC Veterinary Research, Vol 13, Iss 1, Pp 1-8 (2017)

Abstract Background Sensitivity to macrocyclic lactones, which are commonly used in veterinary clinics, was first found in Rough Collies, and was attributed in 2001 to a 4 bp deletion in the MDR1 gene. The list of affected breeds currently includes 1

Externí odkaz: https://doaj.org/article/0a79453a7bf84c9fa932745f779735c0

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POLD1 and POLE Gene Mutations in Jewish Cohorts of Early-Onset Colorectal Cancer and of Multiple Colorectal Adenomas

Autor: Guy Rosner, Naomi Fliss-Issakov, Shai Carmi, Nathan Gluck, Oren Shibolet, Sivan Aharon-Caspi, Dani Bercovich, Revital Kariv, Merav Ben-Yehoyada, Efrat Kellerman, Hana Strul

Publikováno v: Diseases of the colon and rectum. 61(9)

Germline mutations in the DNA polymerase genes POLD1 and POLE confer high risk for multiple colorectal adenomas and colorectal cancer. However, prevalence and the clinical phenotype of mutation carriers are still not fully characterized.The purpose o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d4e0296f8c49cb833f0e29686c52504
https://pubmed.ncbi.nlm.nih.gov/30086056

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Frequency of canine nt230(del4) MDR1 mutation in prone pure breeds, their crosses and mongrels in Israel - insights from a worldwide comparative perspective

Autor: Izhar Ben-Shlomo, Aviad Stoler, Efrat Kellerman, Yossy Machluf, Dani Bercovich, Arava Aderet, Yoram Plotsky, Yaron Dekel, Gal Elhalal, Oshrat Noked Partouche, Daniel Baumel

Publikováno v: BMC Veterinary Research, Vol 13, Iss 1, Pp 1-8 (2017)
BMC Veterinary Research

Background Sensitivity to macrocyclic lactones, which are commonly used in veterinary clinics, was first found in Rough Collies, and was attributed in 2001 to a 4 bp deletion in the MDR1 gene. The list of affected breeds currently includes 13 breeds.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b63c59983a15971a0a5ff9f3bd2bc1ee
https://doi.org/10.1186/s12917-017-1251-9

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Substrate profiling of human vaccinia-related kinases identifies coilin, a Cajal body nuclear protein, as a phosphorylation target with neurological implications

Autor: Paul Renbaum, Marta Vázquez-Cedeira, Pedro A. Lazo, Ephrat Levy-Lahad, Marta Sanz-García, Efrat Kellerman

Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
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Protein phosphorylation by kinases plays a central role in the regulation and coordination of multiple biological processes. In general, knowledge on kinase specificity is restricted to substrates identified in the context of specific cellular respon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48c1ed5394f40ccab21f3934036ae4c0
http://hdl.handle.net/10261/63101

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Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene

Autor: Ranit Jaron, Reeval Segel, Dan Geiger, Ephrat Levy-Lahad, Mary Claire King, Efrat Kellerman, Ming Lee, Paul Renbaum

Publikováno v: American journal of human genetics. 85(2)

The spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of disorders characterized by degeneration and loss of anterior horn cells in the spinal cord, leading to muscle weakness and atrophy. Spinal muscular atrophy w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edf81c89bbc88ace9c1597e8f52bdb90
https://pubmed.ncbi.nlm.nih.gov/19646678

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