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Andrew von Niederhausern

Showing results (1-10 of 9) with videos related to

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American Journal of Human Genetics|March 13, 2003
Rapid direct sequence analysis of the dystrophin geneKevin M Flanigan, Andrew von Niederhausern, Diane M Dunn, et al.
Journal of Human Genetics|January 11, 2003
Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcriptDiane M Dunn, Tomoaki Ishigami, James Pankow, et al.
Genome Research|September 15, 2004
Pattern of sequence variation across 213 environmental response genesRobert J Livingston, Andrew von Niederhausern, Anil G Jegga, et al.
Neuromuscular Disorders : NMD|October 2, 2009
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophyKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|May 14, 2009
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypesTimothy B Baker, Robert B Weiss, Daniel Bolt, et al.
Plos Genetics|July 12, 2008
A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addictionRobert B Weiss, Timothy B Baker, Dale S Cannon, et al.
Human Mutation|October 6, 2011
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD geneKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Neuromuscular Disorders : NMD|July 16, 2010
Clinical and genetic characterization of manifesting carriers of DMD mutationsPayam Soltanzadeh, Michael J Friez, Diane Dunn, et al.
Human Mutation|November 26, 2009
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohortKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Human Genetics|March 13, 2003
Rapid direct sequence analysis of the dystrophin geneKevin M Flanigan, Andrew von Niederhausern, Diane M Dunn, et al.
Journal of Human Genetics|January 11, 2003
Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcriptDiane M Dunn, Tomoaki Ishigami, James Pankow, et al.
Genome Research|September 15, 2004
Pattern of sequence variation across 213 environmental response genesRobert J Livingston, Andrew von Niederhausern, Anil G Jegga, et al.
Neuromuscular Disorders : NMD|October 2, 2009
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophyKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|May 14, 2009
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypesTimothy B Baker, Robert B Weiss, Daniel Bolt, et al.
Plos Genetics|July 12, 2008
A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addictionRobert B Weiss, Timothy B Baker, Dale S Cannon, et al.
Human Mutation|October 6, 2011
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD geneKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Neuromuscular Disorders : NMD|July 16, 2010
Clinical and genetic characterization of manifesting carriers of DMD mutationsPayam Soltanzadeh, Michael J Friez, Diane Dunn, et al.
Human Mutation|November 26, 2009
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohortKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Pageof 1