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Stephan Rust

Showing results (31-40 of 53) with videos related to

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Atherosclerosis|May 30, 2006
Unsaturated fatty acids suppress the expression of the ATP-binding cassette transporter G1 (ABCG1) and ABCA1 genes via an LXR/RXR responsive elementYoshinari Uehara, Shin-ichiro Miura, Arnold von Eckardstein, et al.
Journal of Inherited Metabolic Disease|June 27, 2021
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolismMelanie Meyer, Jana C Hollenbeck, Janine Reunert, et al.
Diabetes|September 28, 2002
Polyunsaturated fatty acids and acetoacetate downregulate the expression of the ATP-binding cassette transporter A1Yoshinari Uehara, Thomas Engel, Zhengchen Li, et al.
Journal of Medical Genetics|June 4, 2020
TMEM16A deficiency: a potentially fatal neonatal disease resulting from impaired chloride currentsJulien H Park, Jiraporn Ousingsawat, Inês Cabrita, et al.
JIMD Reports|August 26, 2015
News on Clinical Details and Treatment in PGM1-CDGEsther Schrapers, Laura C Tegtmeyer, Gunter Simic-Schleicher, et al.
Circulation Research|February 22, 2017
A Mutation in the G-Protein Gene <i>GNB2</i> Causes Familial Sinus Node and Atrioventricular Conduction DysfunctionBirgit Stallmeyer, Johanna Kuß, Stefan Kotthoff, et al.
Brain : a Journal of Neurology|July 24, 2019
SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosisJulien H Park, Christiane Elpers, Janine Reunert, et al.
Journal of Medical Genetics|April 26, 2020
TRAPγ-CDG shows asymmetric glycosylation and an effect on processing of proteins required in higher organismsSabine Dittner-Moormann, Charles Marques Lourenco, Janine Reunert, et al.
European Journal of Human Genetics : EJHG|November 30, 2006
Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS studySimona Barlera, Claudia Specchia, Martin Farrall, et al.
Human Molecular Genetics|December 1, 2007
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9pHelen M Broadbent, John F Peden, Stefan Lorkowski, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Atherosclerosis|May 30, 2006
Unsaturated fatty acids suppress the expression of the ATP-binding cassette transporter G1 (ABCG1) and ABCA1 genes via an LXR/RXR responsive elementYoshinari Uehara, Shin-ichiro Miura, Arnold von Eckardstein, et al.
Journal of Inherited Metabolic Disease|June 27, 2021
3-Hydroxyisobutyrate dehydrogenase (HIBADH) deficiency-A novel disorder of valine metabolismMelanie Meyer, Jana C Hollenbeck, Janine Reunert, et al.
Diabetes|September 28, 2002
Polyunsaturated fatty acids and acetoacetate downregulate the expression of the ATP-binding cassette transporter A1Yoshinari Uehara, Thomas Engel, Zhengchen Li, et al.
Journal of Medical Genetics|June 4, 2020
TMEM16A deficiency: a potentially fatal neonatal disease resulting from impaired chloride currentsJulien H Park, Jiraporn Ousingsawat, Inês Cabrita, et al.
JIMD Reports|August 26, 2015
News on Clinical Details and Treatment in PGM1-CDGEsther Schrapers, Laura C Tegtmeyer, Gunter Simic-Schleicher, et al.
Circulation Research|February 22, 2017
A Mutation in the G-Protein Gene <i>GNB2</i> Causes Familial Sinus Node and Atrioventricular Conduction DysfunctionBirgit Stallmeyer, Johanna Kuß, Stefan Kotthoff, et al.
Brain : a Journal of Neurology|July 24, 2019
SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosisJulien H Park, Christiane Elpers, Janine Reunert, et al.
Journal of Medical Genetics|April 26, 2020
TRAPγ-CDG shows asymmetric glycosylation and an effect on processing of proteins required in higher organismsSabine Dittner-Moormann, Charles Marques Lourenco, Janine Reunert, et al.
European Journal of Human Genetics : EJHG|November 30, 2006
Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS studySimona Barlera, Claudia Specchia, Martin Farrall, et al.
Human Molecular Genetics|December 1, 2007
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9pHelen M Broadbent, John F Peden, Stefan Lorkowski, et al.
Pageof 6