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Cell Research
|
January 13, 2018
Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disorders
Jasmine 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-telangiectasia
Shelly 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 ferroportin
Sara 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 mutations
Joshi 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 Syndrome
Iddo 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 growth
Yael Nemlich, Eyal Greenberg, Rona Ortenberg, et al.
Nature
|
February 11, 2016
The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNA
Dan 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 1
Lina 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 system
Efrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.
Page
of 30
Search research articles
Search
Showing results (271-280 of 297) with videos related to
Sort By:
Page
of 30
Cell Research
|
January 13, 2018
Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disorders
Jasmine 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-telangiectasia
Shelly 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 ferroportin
Sara 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 mutations
Joshi 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 Syndrome
Iddo 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 growth
Yael Nemlich, Eyal Greenberg, Rona Ortenberg, et al.
Nature
|
February 11, 2016
The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNA
Dan 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 1
Lina 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 system
Efrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.
Page
of 30