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Eva Gak

Showing results (11-20 of 18) with videos related to

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Journal of Applied Genetics|January 16, 2014
The VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populationsSophia Sominsky, Michael Korostishevsky, Daniel Kurnik, et al.
Plos One|June 23, 2011
Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutationsManuela Vecsler, Bruria Ben Zeev, Igor Nudelman, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasmsDorit Lev, Yuval Weigl, Mariana Hasan, et al.
Thrombosis and Haemostasis|August 9, 2012
Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose predictionDaniel Kurnik, Husam Qasim, Sophie Sominsky, et al.
Blood|November 18, 2006
A coding VKORC1 Asp36Tyr polymorphism predisposes to warfarin resistanceRonen Loebstein, Ilana Dvoskin, Hillel Halkin, et al.
Archives of Women'S Mental Health|June 19, 2013
Association between a common CYP17A1 haplotype and anxiety in female anorexia nervosaEfrat Czerniak, Michael Korostishevsky, Amos Frisch, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish populationMaya Koronyo-Hamaoui, Eva Gak, Daniel Stein, et al.
Journal of Psychiatric Research|September 15, 2005
Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosaMaya Koronyo-Hamaoui, Amos Frisch, Daniel Stein, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Applied Genetics|January 16, 2014
The VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populationsSophia Sominsky, Michael Korostishevsky, Daniel Kurnik, et al.
Plos One|June 23, 2011
Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutationsManuela Vecsler, Bruria Ben Zeev, Igor Nudelman, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasmsDorit Lev, Yuval Weigl, Mariana Hasan, et al.
Thrombosis and Haemostasis|August 9, 2012
Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose predictionDaniel Kurnik, Husam Qasim, Sophie Sominsky, et al.
Blood|November 18, 2006
A coding VKORC1 Asp36Tyr polymorphism predisposes to warfarin resistanceRonen Loebstein, Ilana Dvoskin, Hillel Halkin, et al.
Archives of Women'S Mental Health|June 19, 2013
Association between a common CYP17A1 haplotype and anxiety in female anorexia nervosaEfrat Czerniak, Michael Korostishevsky, Amos Frisch, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish populationMaya Koronyo-Hamaoui, Eva Gak, Daniel Stein, et al.
Journal of Psychiatric Research|September 15, 2005
Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosaMaya Koronyo-Hamaoui, Amos Frisch, Daniel Stein, et al.
Pageof 2