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Rune R Frants

Showing results (91-100 of 104) with videos related to

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Annals of Neurology|February 27, 2010
High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L miceArn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, et al.
Thrombosis and Haemostasis|December 8, 2007
The influence of established genetic variation in the haemostatic system on clinical restenosis after percutaneous coronary interventionsDouwe Pons, Pascalle S Monraats, Moniek P M de Maat, et al.
Pharmacogenetics and Genomics|September 27, 2006
Inflammation and apoptosis genes and the risk of restenosis after percutaneous coronary interventionPascalle S Monraats, Florentine de Vries, Laura W de Jong, et al.
Circulation|October 19, 2005
Genetic inflammatory factors predict restenosis after percutaneous coronary interventionsPascalle S Monraats, Nuno M M Pires, Willem R P Agema, et al.
Journal of the American College of Cardiology|September 20, 2005
Lipoprotein lipase gene polymorphisms and the risk of target vessel revascularization after percutaneous coronary interventionPascalle S Monraats, Jamal S Rana, Melchior C Nierman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 2, 2005
Tumor necrosis factor-alpha plays an important role in restenosis developmentPascalle S Monraats, Nuno M M Pires, Abbey Schepers, et al.
American Journal of Human Genetics|May 21, 2011
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2Jessica C de Greef, Jun Wang, Judit Balog, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Annals of Neurology|February 27, 2010
High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L miceArn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, et al.
Thrombosis and Haemostasis|December 8, 2007
The influence of established genetic variation in the haemostatic system on clinical restenosis after percutaneous coronary interventionsDouwe Pons, Pascalle S Monraats, Moniek P M de Maat, et al.
Pharmacogenetics and Genomics|September 27, 2006
Inflammation and apoptosis genes and the risk of restenosis after percutaneous coronary interventionPascalle S Monraats, Florentine de Vries, Laura W de Jong, et al.
Circulation|October 19, 2005
Genetic inflammatory factors predict restenosis after percutaneous coronary interventionsPascalle S Monraats, Nuno M M Pires, Willem R P Agema, et al.
Journal of the American College of Cardiology|September 20, 2005
Lipoprotein lipase gene polymorphisms and the risk of target vessel revascularization after percutaneous coronary interventionPascalle S Monraats, Jamal S Rana, Melchior C Nierman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 2, 2005
Tumor necrosis factor-alpha plays an important role in restenosis developmentPascalle S Monraats, Nuno M M Pires, Abbey Schepers, et al.
American Journal of Human Genetics|May 21, 2011
Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2Jessica C de Greef, Jun Wang, Judit Balog, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Human Molecular Genetics|August 5, 2008
A high-density association screen of 155 ion transport genes for involvement with common migraineDale R Nyholt, K Steven LaForge, Mikko Kallela, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Pageof 11