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Thomas Meitinger

Showing results (181-190 of 508) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
Frontiers in Medicine|September 19, 2022
The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experienceJasmina Ćomić, Korbinian M Riedhammer, Roman Günthner, et al.
American Journal of Human Genetics|December 4, 2014
Absence of BiP co-chaperone DNAJC3 causes diabetes mellitus and multisystemic neurodegenerationMatthis Synofzik, Tobias B Haack, Robert Kopajtich, et al.
Plos One|January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disordersMichael Zech, Georg Nübling, Florian Castrop, et al.
American Journal of Human Genetics|January 31, 2012
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndromeJohannes A Mayr, Tobias B Haack, Elisabeth Graf, et al.
Molecular Metabolism|February 4, 2018
Genome-wide analysis of PDX1 target genes in human pancreatic progenitorsXianming Wang, Michael Sterr, Ingo Burtscher, et al.
European Journal of Human Genetics : EJHG|August 30, 2012
Dilution of candidates: the case of iron-related genes in restless legs syndromeKonrad Oexle, Barbara Schormair, Janina S Ried, et al.
Nature Genetics|December 29, 2009
A genome-wide perspective of genetic variation in human metabolismThomas Illig, Christian Gieger, Guangju Zhai, et al.
European Journal of Public Health|February 15, 2022
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
Plos Genetics|January 13, 2010
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levelsWilmar Igl, Asa Johansson, James F Wilson, et al.
Pageof 51

Showing results (181-190 of 508) with videos related to

Sort By:
Pageof 51
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
Frontiers in Medicine|September 19, 2022
The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experienceJasmina Ćomić, Korbinian M Riedhammer, Roman Günthner, et al.
American Journal of Human Genetics|December 4, 2014
Absence of BiP co-chaperone DNAJC3 causes diabetes mellitus and multisystemic neurodegenerationMatthis Synofzik, Tobias B Haack, Robert Kopajtich, et al.
Plos One|January 4, 2014
Niemann-Pick C disease gene mutations and age-related neurodegenerative disordersMichael Zech, Georg Nübling, Florian Castrop, et al.
American Journal of Human Genetics|January 31, 2012
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndromeJohannes A Mayr, Tobias B Haack, Elisabeth Graf, et al.
Molecular Metabolism|February 4, 2018
Genome-wide analysis of PDX1 target genes in human pancreatic progenitorsXianming Wang, Michael Sterr, Ingo Burtscher, et al.
European Journal of Human Genetics : EJHG|August 30, 2012
Dilution of candidates: the case of iron-related genes in restless legs syndromeKonrad Oexle, Barbara Schormair, Janina S Ried, et al.
Nature Genetics|December 29, 2009
A genome-wide perspective of genetic variation in human metabolismThomas Illig, Christian Gieger, Guangju Zhai, et al.
European Journal of Public Health|February 15, 2022
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
Plos Genetics|January 13, 2010
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levelsWilmar Igl, Asa Johansson, James F Wilson, et al.
Pageof 51