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Eva Gak

Showing results (1-10 of 18) with videos related to

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Pharmacogenomics|October 16, 2008
Shifting paradigms in the pharmacogenetics of warfarinEva Gak, Hillel Halkin
Parkinsonism & Related Disorders|February 5, 2011
Benign hereditary chorea: an updateRivka Inzelberg, Moran Weinberger, Eva Gak
Pharmacogenomics|December 5, 2009
10 years of oral anticoagulant pharmacogenomics: what difference will it make? A critical appraisalDaniel Kurnik, Ronen Loebstein, Hillel Halkin, et al.
Blood|March 26, 2008
VKORC1 Asp36Tyr warfarin resistance marker is common in Ethiopian individualsEleni Aklillu, Cheryl Leong, Ronen Loebstein, et al.
Epigenetics|January 23, 2010
MeCP2 deficiency downregulates specific nuclear proteins that could be partially recovered by valproic acid in vitroManuela Vecsler, Amos J Simon, Ninette Amariglio, et al.
Epilepsia|May 25, 2010
Epilepsy in Rett syndrome---the experience of a National Rett CenterAndreea Nissenkorn, Eva Gak, Manuela Vecsler, et al.
Thrombosis and Haemostasis|February 24, 2006
Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarinManuela Vecsler, Ronen Loebstein, Shlomo Almog, et al.
Clinical Pharmacology and Therapeutics|May 19, 2005
Common genetic variants of microsomal epoxide hydrolase affect warfarin dose requirements beyond the effect of cytochrome P450 2C9Ronen Loebstein, Manuela Vecsler, Daniel Kurnik, et al.
Human Genetics|September 1, 2005
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosisLiron Abuhatzira, Kirill Makedonski, Yael Petel Galil, et al.
Psychiatric Genetics|September 10, 2003
Association study of CAG repeats in the KCNN3 gene in Israeli patients with major psychosisMichael Ritsner, Sharon Amir, Maya Koronyo-Hamaoui, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Pharmacogenomics|October 16, 2008
Shifting paradigms in the pharmacogenetics of warfarinEva Gak, Hillel Halkin
Parkinsonism & Related Disorders|February 5, 2011
Benign hereditary chorea: an updateRivka Inzelberg, Moran Weinberger, Eva Gak
Pharmacogenomics|December 5, 2009
10 years of oral anticoagulant pharmacogenomics: what difference will it make? A critical appraisalDaniel Kurnik, Ronen Loebstein, Hillel Halkin, et al.
Blood|March 26, 2008
VKORC1 Asp36Tyr warfarin resistance marker is common in Ethiopian individualsEleni Aklillu, Cheryl Leong, Ronen Loebstein, et al.
Epigenetics|January 23, 2010
MeCP2 deficiency downregulates specific nuclear proteins that could be partially recovered by valproic acid in vitroManuela Vecsler, Amos J Simon, Ninette Amariglio, et al.
Epilepsia|May 25, 2010
Epilepsy in Rett syndrome---the experience of a National Rett CenterAndreea Nissenkorn, Eva Gak, Manuela Vecsler, et al.
Thrombosis and Haemostasis|February 24, 2006
Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarinManuela Vecsler, Ronen Loebstein, Shlomo Almog, et al.
Clinical Pharmacology and Therapeutics|May 19, 2005
Common genetic variants of microsomal epoxide hydrolase affect warfarin dose requirements beyond the effect of cytochrome P450 2C9Ronen Loebstein, Manuela Vecsler, Daniel Kurnik, et al.
Human Genetics|September 1, 2005
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosisLiron Abuhatzira, Kirill Makedonski, Yael Petel Galil, et al.
Psychiatric Genetics|September 10, 2003
Association study of CAG repeats in the KCNN3 gene in Israeli patients with major psychosisMichael Ritsner, Sharon Amir, Maya Koronyo-Hamaoui, et al.
Pageof 2