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Shay Ben-Shachar

Showing results (51-60 of 96) with videos related to

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Inflammatory Bowel Diseases|October 11, 2013
Gene expression profiles of ileal inflammatory bowel disease correlate with disease phenotype and advance understanding of its immunopathogenesisShay Ben-Shachar, Henit Yanai, Liran Baram, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutationNoam Domniz, Liat Ries Levavi, Michal Berkenstadt, et al.
Plos One|August 19, 2016
MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease PhenotypesShay Ben-Shachar, Henit Yanai, Hadas Sherman Horev, et al.
Heart Rhythm|July 23, 2013
Fever-induced Brugada pattern: how common is it and what does it mean?Arnon Adler, Guy Topaz, Karin Heller, et al.
Plos One|October 19, 2016
Correction: MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease PhenotypesShay Ben-Shachar, Henit Yanai, Hadas Sherman Horev, et al.
Molecular Genetics and Metabolism|December 15, 2015
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian originEyal Reinstein, Pola Smirin-Yosef, Irina Lagovsky, et al.
Journal of Perinatal Medicine|July 29, 2020
The yield of chromosomal microarray testing for cases of abnormal fetal head circumferenceYael Pasternak, Amihood Singer, Idit Maya, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 26, 2018
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray resultsLena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, et al.
Clinical Genetics|December 30, 2021
Di-genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predispositionOrli Michaeli, Hagay Ladany, Ayelet Erez, et al.
European Journal of Human Genetics : EJHG|April 10, 2021
Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestationsMoran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Inflammatory Bowel Diseases|October 11, 2013
Gene expression profiles of ileal inflammatory bowel disease correlate with disease phenotype and advance understanding of its immunopathogenesisShay Ben-Shachar, Henit Yanai, Liran Baram, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2021
Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutationNoam Domniz, Liat Ries Levavi, Michal Berkenstadt, et al.
Plos One|August 19, 2016
MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease PhenotypesShay Ben-Shachar, Henit Yanai, Hadas Sherman Horev, et al.
Heart Rhythm|July 23, 2013
Fever-induced Brugada pattern: how common is it and what does it mean?Arnon Adler, Guy Topaz, Karin Heller, et al.
Plos One|October 19, 2016
Correction: MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease PhenotypesShay Ben-Shachar, Henit Yanai, Hadas Sherman Horev, et al.
Molecular Genetics and Metabolism|December 15, 2015
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian originEyal Reinstein, Pola Smirin-Yosef, Irina Lagovsky, et al.
Journal of Perinatal Medicine|July 29, 2020
The yield of chromosomal microarray testing for cases of abnormal fetal head circumferenceYael Pasternak, Amihood Singer, Idit Maya, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 26, 2018
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray resultsLena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, et al.
Clinical Genetics|December 30, 2021
Di-genic inheritance of germline POLE and PMS2 pathogenic variants causes a unique condition associated with pediatric cancer predispositionOrli Michaeli, Hagay Ladany, Ayelet Erez, et al.
European Journal of Human Genetics : EJHG|April 10, 2021
Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestationsMoran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, et al.
Pageof 10