Resultados de procura - Andrew von Niederhausern
- Mostrando 1 - 8 Resultados de 8
-
1
-
2
Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript por Diane M. Dunn, Tomoaki Ishigami, James S. Pankow, Andrew von Niederhausern, Jonathan K. Alder, Steven C. Hunt, Mark Leppert, J.-M. Lalouel, Robert B. Weiss
Publicado 2002Artigo -
3
Pattern of Sequence Variation Across 213 Environmental Response Genes por Robert Livingston, Andrew von Niederhausern, Anil G. Jegga, Dana C. Crawford, Christopher S. Carlson, Mark J. Rieder, Sivakumar Gowrisankar, Bruce J. Aronow, Robert B. Weiss, Deborah A. Nickerson
Publicado 2004Artigo -
4
Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes por Timothy B. Baker, Robert B. Weiss, Daniel M. Bolt, Andrew von Niederhausern, Michael C. Fiore, Diane M. Dunn, Megan E. Piper, Nori Matsunami, Stevens S. Smith, Hilary Coon, William M. McMahon, Mary Beth Scholand, Nanda Singh, John R. Hoidal, Su‐Young Kim, Mark Leppert, Dale S. Cannon
Publicado 2009Artigo -
5
A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction por Robert B. Weiss, Timothy B. Baker, Dale S. Cannon, Andrew von Niederhausern, Diane M. Dunn, Nori Matsunami, Nanda A. Singh, Lisa Baird, Hilary Coon, William M. McMahon, Megan E. Piper, Michael C. Fiore, Mary Beth Scholand, John E. Connett, Richard E. Kanner, Lorise C. Gahring, Scott W. Rogers, John R. Hoidal, Mark Leppert
Publicado 2008Artigo -
6
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene por Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Payam Soltanzadeh, Michael Howard, Jacinda B. Sampson, Kathryn J. Swoboda, Mark B. Bromberg, Jerry R. Mendell, Laura E. Taylor, Christine B. Anderson, Alan Pestronk, Julaine Florence, Anne M. Connolly, Katherine D. Mathews, Brenda Wong, Richard S. Finkel, Carsten G. Bönnemann, John Day, Craig M. McDonald, Robert B. Weiss
Publicado 2010Artigo -
7
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort por Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Payam Soltanzadeh, Eduard Gappmaier, Michael Howard, Jacinda B. Sampson, Jerry R. Mendell, Cheryl Wall, Wendy King, Alan Pestronk, Julaine Florence, Anne M. Connolly, Katherine D. Mathews, Carrie Stephan, Karla S. Laubenthal, Brenda Wong, P. Morehart, Amy Meyer, Richard S. Finkel, Carsten G. Bönnemann, Līvija Medne, John Day, Joline Dalton, Marcia K. Margolis, Veronica J. Hinton, Robert B. Weiss
Publicado 2009Artigo -
8
Clinical and genetic characterization of manifesting carriers of DMD mutations por Payam Soltanzadeh, Michael J. Friez, Diane M. Dunn, Andrew von Niederhausern, Olga L. Gurvich, Kathryn J. Swoboda, Jacinda B. Sampson, Alan Pestronk, Anne M. Connolly, Julaine Florence, Richard S. Finkel, Carsten G. Bönnemann, Līvija Medne, Jerry R. Mendell, Katherine D. Mathews, Brenda Wong, Michael D. Sussman, Jonathan Zonana, Karen Kovak, Sídney M. Gospe, Eduard Gappmaier, Laura E. Taylor, Michael Howard, Robert B. Weiss, Kevin M. Flanigan
Publicado 2010Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Gene
Genetics
Mutation
Duchenne muscular dystrophy
Exon
Muscular dystrophy
Point mutation
Alternative splicing
Dystrophin
Genotype
Haplotype
Medicine
Missense mutation
Nonsense mutation
Addiction
Exon skipping
Internal medicine
Nicotine
Pathology
Phenotype
Psychiatry
RNA
RNA splicing
Smoking cessation
Bioinformatics
Candidate gene
Carrier testing
Cigarette smoking
Clinical psychology