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Gershoni

Showing results (191-200 of 497) with videos related to

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Genetic Testing and Molecular Biomarkers|June 11, 2014
"I do not want my baby to suffer as I did"; prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: a case report and genetic counseling considerationsEfrat Dagan, Ruth Gershoni-Baruch, Alina Kurolap, et al.
Computer Methods and Programs in Biomedicine|January 18, 2024
Mechanical impact of epiretinal membranes on the retina utilizing finite element analysisSara Naftali, Keren Della Rocca, Assaf Gershoni, et al.
Journal of Human Virology|April 9, 1999
Prevalence of a CCR5 gene 32-bp deletion in an Israeli cohort of HIV-1-infected and uninfected hemophilia patientsR Kantor, A Barzilai, D Varon, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 1997
Helical epitopes determined by low-stringency antibody screening of a combinatorial peptide libraryB Stern, G Denisova, D Buyaner, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1984
Binding of alpha-bungarotoxin to proteolytic fragments of the alpha subunit of Torpedo acetylcholine receptor analyzed by protein transfer on positively charged membrane filtersP T Wilson, J M Gershoni, E Hawrot, et al.
The Journal of Clinical Endocrinology and Metabolism|July 21, 2005
Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan JewsTamar Paperna, Ruth Gershoni-Baruch, Kader Badarneh, et al.
Molecular & Cellular Proteomics : MCP|December 15, 2015
Neurodegeneration and Alzheimer's disease (AD). What Can Proteomics Tell Us About the Alzheimer's Brain?Guillermo Moya-Alvarado, Noga Gershoni-Emek, Eran Perlson, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Congenital permanent diabetes: a different type of diabetes?N Shehadeh, R Gershoni-Baruch, H Mandel, et al.
American Journal of Medical Genetics|April 27, 2002
Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variabilityRuth Gershoni-Baruch, Marwan Shinawi, Hussein Shamaly, et al.
Clinical and Experimental Rheumatology|October 3, 2009
The 3435T polymorphism in the ABCB1 gene and colchicine unresponsiveness in familial Mediterranean feverY Bezalel, R Gershoni-Baruch, E Dagan, et al.
Pageof 50

Showing results (191-200 of 497) with videos related to

Sort By:
Pageof 50
Genetic Testing and Molecular Biomarkers|June 11, 2014
"I do not want my baby to suffer as I did"; prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: a case report and genetic counseling considerationsEfrat Dagan, Ruth Gershoni-Baruch, Alina Kurolap, et al.
Computer Methods and Programs in Biomedicine|January 18, 2024
Mechanical impact of epiretinal membranes on the retina utilizing finite element analysisSara Naftali, Keren Della Rocca, Assaf Gershoni, et al.
Journal of Human Virology|April 9, 1999
Prevalence of a CCR5 gene 32-bp deletion in an Israeli cohort of HIV-1-infected and uninfected hemophilia patientsR Kantor, A Barzilai, D Varon, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 1997
Helical epitopes determined by low-stringency antibody screening of a combinatorial peptide libraryB Stern, G Denisova, D Buyaner, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1984
Binding of alpha-bungarotoxin to proteolytic fragments of the alpha subunit of Torpedo acetylcholine receptor analyzed by protein transfer on positively charged membrane filtersP T Wilson, J M Gershoni, E Hawrot, et al.
The Journal of Clinical Endocrinology and Metabolism|July 21, 2005
Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan JewsTamar Paperna, Ruth Gershoni-Baruch, Kader Badarneh, et al.
Molecular & Cellular Proteomics : MCP|December 15, 2015
Neurodegeneration and Alzheimer's disease (AD). What Can Proteomics Tell Us About the Alzheimer's Brain?Guillermo Moya-Alvarado, Noga Gershoni-Emek, Eran Perlson, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Congenital permanent diabetes: a different type of diabetes?N Shehadeh, R Gershoni-Baruch, H Mandel, et al.
American Journal of Medical Genetics|April 27, 2002
Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variabilityRuth Gershoni-Baruch, Marwan Shinawi, Hussein Shamaly, et al.
Clinical and Experimental Rheumatology|October 3, 2009
The 3435T polymorphism in the ABCB1 gene and colchicine unresponsiveness in familial Mediterranean feverY Bezalel, R Gershoni-Baruch, E Dagan, et al.
Pageof 50