Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Gideon Rechavi

Showing results (271-280 of 297) with videos related to

Pageof 30
Sort By:
Cell Research|January 13, 2018
Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disordersJasmine Jacob-Hirsch, Eran Eyal, Binyamin A Knisbacher, et al.
Human Molecular Genetics|September 10, 2005
Impaired genomic stability and increased oxidative stress exacerbate different features of Ataxia-telangiectasiaShelly Ziv, Ori Brenner, Ninette Amariglio, et al.
Blood|February 15, 2007
Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportinSara Gardenghi, Maria F Marongiu, Pedro Ramos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 12, 2017
Disruption of Thrombocyte and T Lymphocyte Development by a Mutation in <i>ARPC1B</i>Raz Somech, Atar Lev, Yu Nee Lee, et al.
European Journal of Human Genetics : EJHG|February 18, 2016
Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutationsJoshi Stephen, Thierry Vilboux, Yael Haberman, et al.
Digestive Diseases and Sciences|February 28, 2018
Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric SyndromeIddo Vardi, Ortal Barel, Michal Sperber, et al.
The Journal of Clinical Investigation|June 4, 2013
MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growthYael Nemlich, Eyal Greenberg, Rona Ortenberg, et al.
Nature|February 11, 2016
The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNADan Dominissini, Sigrid Nachtergaele, Sharon Moshitch-Moshkovitz, et al.
American Journal of Human Genetics|January 10, 2012
Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1Lina Basel-Vanagaite, Noam Zevit, Adi Har Zahav, et al.
American Journal of Human Genetics|November 2, 2010
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic systemEfrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.
Pageof 30

Showing results (271-280 of 297) with videos related to

Sort By:
Pageof 30
Cell Research|January 13, 2018
Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disordersJasmine Jacob-Hirsch, Eran Eyal, Binyamin A Knisbacher, et al.
Human Molecular Genetics|September 10, 2005
Impaired genomic stability and increased oxidative stress exacerbate different features of Ataxia-telangiectasiaShelly Ziv, Ori Brenner, Ninette Amariglio, et al.
Blood|February 15, 2007
Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportinSara Gardenghi, Maria F Marongiu, Pedro Ramos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 12, 2017
Disruption of Thrombocyte and T Lymphocyte Development by a Mutation in <i>ARPC1B</i>Raz Somech, Atar Lev, Yu Nee Lee, et al.
European Journal of Human Genetics : EJHG|February 18, 2016
Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutationsJoshi Stephen, Thierry Vilboux, Yael Haberman, et al.
Digestive Diseases and Sciences|February 28, 2018
Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric SyndromeIddo Vardi, Ortal Barel, Michal Sperber, et al.
The Journal of Clinical Investigation|June 4, 2013
MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growthYael Nemlich, Eyal Greenberg, Rona Ortenberg, et al.
Nature|February 11, 2016
The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNADan Dominissini, Sigrid Nachtergaele, Sharon Moshitch-Moshkovitz, et al.
American Journal of Human Genetics|January 10, 2012
Transient infantile hypertriglyceridemia, fatty liver, and hepatic fibrosis caused by mutated GPD1, encoding glycerol-3-phosphate dehydrogenase 1Lina Basel-Vanagaite, Noam Zevit, Adi Har Zahav, et al.
American Journal of Human Genetics|November 2, 2010
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic systemEfrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.
Pageof 30