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Rune R Frants

Showing results (81-90 of 104) with videos related to

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Science (New York, N.Y.)|August 21, 2010
A unifying genetic model for facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, et al.
European Heart Journal|July 3, 2004
Current PTCA practice and clinical outcomes in The Netherlands: the real world in the pre-drug-eluting stent eraWillem R P Agema, Pascalle S Monraats, Aeilko H Zwinderman, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesFemke A de Snoo, Jouke-Jan Hottenga, Elizabeth M Gillanders, et al.
Thrombosis and Haemostasis|March 1, 2005
-455G/A polymorphism and preprocedural plasma levels of fibrinogen show no association with the risk of clinical restenosis in patients with coronary stent placementPascalle S Monraats, Jamal S Rana, Aeilko H Zwinderman, et al.
Plos Genetics|April 18, 2013
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDYvonne D Krom, Peter E Thijssen, Janet M Young, et al.
Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.
European Journal of Human Genetics : EJHG|May 3, 2007
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraineKaate R J Vanmolkot, Anine H Stam, Ashok Raman, et al.
Plos Genetics|July 14, 2009
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD)Weihua Zeng, Jessica C de Greef, Yen-Yun Chen, et al.
European Journal of Human Genetics : EJHG|March 16, 2006
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraineKaate R J Vanmolkot, Esther E Kors, Ulku Turk, et al.
Expert Opinion on Therapeutic Targets|January 26, 2010
Vitamin D receptor: a new risk marker for clinical restenosis after percutaneous coronary interventionPascalle S Monraats, Yue Fang, Douwe Pons, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
Science (New York, N.Y.)|August 21, 2010
A unifying genetic model for facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Patrick J van der Vliet, Rinse Klooster, et al.
European Heart Journal|July 3, 2004
Current PTCA practice and clinical outcomes in The Netherlands: the real world in the pre-drug-eluting stent eraWillem R P Agema, Pascalle S Monraats, Aeilko H Zwinderman, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesFemke A de Snoo, Jouke-Jan Hottenga, Elizabeth M Gillanders, et al.
Thrombosis and Haemostasis|March 1, 2005
-455G/A polymorphism and preprocedural plasma levels of fibrinogen show no association with the risk of clinical restenosis in patients with coronary stent placementPascalle S Monraats, Jamal S Rana, Aeilko H Zwinderman, et al.
Plos Genetics|April 18, 2013
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHDYvonne D Krom, Peter E Thijssen, Janet M Young, et al.
Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.
European Journal of Human Genetics : EJHG|May 3, 2007
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraineKaate R J Vanmolkot, Anine H Stam, Ashok Raman, et al.
Plos Genetics|July 14, 2009
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD)Weihua Zeng, Jessica C de Greef, Yen-Yun Chen, et al.
European Journal of Human Genetics : EJHG|March 16, 2006
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraineKaate R J Vanmolkot, Esther E Kors, Ulku Turk, et al.
Expert Opinion on Therapeutic Targets|January 26, 2010
Vitamin D receptor: a new risk marker for clinical restenosis after percutaneous coronary interventionPascalle S Monraats, Yue Fang, Douwe Pons, et al.
Pageof 11