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Rune R Frants

Showing results (31-40 of 104) with videos related to

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Brain Research|February 27, 2007
Redundancy of Cav2.1 channel accessory subunits in transmitter release at the mouse neuromuscular junctionSimon Kaja, Boyan Todorov, Rob C G van de Ven, et al.
Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, et al.
Atherosclerosis|September 15, 2005
Genomic analysis of the response of mouse models to high-fat feeding shows a major role of nuclear receptors in the simultaneous regulation of lipid and inflammatory genesArja J Kreeft, Corina J A Moen, Gordon Porter, et al.
Journal of Child Neurology|April 11, 2014
Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical featuresMałgorzata Dorobek, Silvère M van der Maarel, Richard J L F Lemmers, et al.
Cephalalgia : an International Journal of Headache|October 27, 2010
A long-term follow-up study of 18 patients with sporadic hemiplegic migraineAnine H Stam, Mark A Louter, Joost Haan, et al.
Genomics|February 7, 2002
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common originMichel van Geel, Morag C Dickson, Amy F Beck, et al.
Human Genetics|December 13, 2005
Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophyMaria Manuela O Tonini, Richard J L F Lemmers, Rita C M Pavanello, et al.
Nutrition & Metabolism|March 30, 2010
High levels of dietary stearate promote adiposity and deteriorate hepatic insulin sensitivitySjoerd Aa van den Berg, Bruno Guigas, Silvia Bijland, et al.
Diabetes Care|January 14, 2010
Genetic architecture of plasma adiponectin overlaps with the genetics of metabolic syndrome-related traitsPeter Henneman, Yurii S Aulchenko, Rune R Frants, et al.
Journal of Neurophysiology|July 16, 2010
Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in miceSimon Kaja, Rob C G Van de Ven, Ludo A M Broos, et al.
Pageof 11

Showing results (31-40 of 104) with videos related to

Sort By:
Pageof 11
Brain Research|February 27, 2007
Redundancy of Cav2.1 channel accessory subunits in transmitter release at the mouse neuromuscular junctionSimon Kaja, Boyan Todorov, Rob C G van de Ven, et al.
Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, et al.
Atherosclerosis|September 15, 2005
Genomic analysis of the response of mouse models to high-fat feeding shows a major role of nuclear receptors in the simultaneous regulation of lipid and inflammatory genesArja J Kreeft, Corina J A Moen, Gordon Porter, et al.
Journal of Child Neurology|April 11, 2014
Early-onset facioscapulohumeral muscular dystrophy type 1 with some atypical featuresMałgorzata Dorobek, Silvère M van der Maarel, Richard J L F Lemmers, et al.
Cephalalgia : an International Journal of Headache|October 27, 2010
A long-term follow-up study of 18 patients with sporadic hemiplegic migraineAnine H Stam, Mark A Louter, Joost Haan, et al.
Genomics|February 7, 2002
Genomic analysis of human chromosome 10q and 4q telomeres suggests a common originMichel van Geel, Morag C Dickson, Amy F Beck, et al.
Human Genetics|December 13, 2005
Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophyMaria Manuela O Tonini, Richard J L F Lemmers, Rita C M Pavanello, et al.
Nutrition & Metabolism|March 30, 2010
High levels of dietary stearate promote adiposity and deteriorate hepatic insulin sensitivitySjoerd Aa van den Berg, Bruno Guigas, Silvia Bijland, et al.
Diabetes Care|January 14, 2010
Genetic architecture of plasma adiponectin overlaps with the genetics of metabolic syndrome-related traitsPeter Henneman, Yurii S Aulchenko, Rune R Frants, et al.
Journal of Neurophysiology|July 16, 2010
Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in miceSimon Kaja, Rob C G Van de Ven, Ludo A M Broos, et al.
Pageof 11