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Thomas Meitinger

Showing results (101-110 of 508) with videos related to

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BMC Genetics|May 5, 2007
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13Susann Friedel, Kathrin Reichwald, André Scherag, et al.
Human Molecular Genetics|January 7, 2015
CRIM1 haploinsufficiency causes defects in eye development in human and mouseFilippo Beleggia, Yun Li, Jieqing Fan, et al.
British Journal of Pharmacology|June 25, 2022
Riociguat attenuates the changes in left ventricular proteome and microRNA profile after experimental aortic stenosis in miceAlexander Benkner, Julia Rüdebusch, Neetika Nath, et al.
European Journal of Human Genetics : EJHG|March 16, 2023
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experienceKorbinian M Riedhammer, Jasmina Ćomić, Velibor Tasic, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole bloodDivya Mehta, Katharina Heim, Christian Herder, et al.
European Journal of Human Genetics : EJHG|June 15, 2017
Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalitiesDiran Herebian, Bader Alhaddad, Annette Seibt, et al.
Human Biology|February 7, 2007
Genetic structure in contemporary south Tyrolean isolated populations revealed by analysis of Y-chromosome, mtDNA, and Alu polymorphismsIrene Pichler, Jakob C Mueller, Stefan A Stefanov, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 19, 2008
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypesMarc Fatar, Mark Stroick, Michael Steffens, et al.
Molecular Genetics and Metabolism|February 13, 2007
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescentsTimo Dirk Müller, Kathrin Reichwald, Anne-Kathrin Wermter, et al.
JIMD Reports|June 21, 2018
A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic EncephalopathyArcangela Iuso, Bader Alhaddad, Corina Weigel, et al.
Pageof 51

Showing results (101-110 of 508) with videos related to

Sort By:
Pageof 51
BMC Genetics|May 5, 2007
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13Susann Friedel, Kathrin Reichwald, André Scherag, et al.
Human Molecular Genetics|January 7, 2015
CRIM1 haploinsufficiency causes defects in eye development in human and mouseFilippo Beleggia, Yun Li, Jieqing Fan, et al.
British Journal of Pharmacology|June 25, 2022
Riociguat attenuates the changes in left ventricular proteome and microRNA profile after experimental aortic stenosis in miceAlexander Benkner, Julia Rüdebusch, Neetika Nath, et al.
European Journal of Human Genetics : EJHG|March 16, 2023
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experienceKorbinian M Riedhammer, Jasmina Ćomić, Velibor Tasic, et al.
European Journal of Human Genetics : EJHG|June 14, 2012
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole bloodDivya Mehta, Katharina Heim, Christian Herder, et al.
European Journal of Human Genetics : EJHG|June 15, 2017
Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalitiesDiran Herebian, Bader Alhaddad, Annette Seibt, et al.
Human Biology|February 7, 2007
Genetic structure in contemporary south Tyrolean isolated populations revealed by analysis of Y-chromosome, mtDNA, and Alu polymorphismsIrene Pichler, Jakob C Mueller, Stefan A Stefanov, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 19, 2008
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypesMarc Fatar, Mark Stroick, Michael Steffens, et al.
Molecular Genetics and Metabolism|February 13, 2007
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescentsTimo Dirk Müller, Kathrin Reichwald, Anne-Kathrin Wermter, et al.
JIMD Reports|June 21, 2018
A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic EncephalopathyArcangela Iuso, Bader Alhaddad, Corina Weigel, et al.
Pageof 51