Rezultati - MaryAnne Anderson
- Showing 1 - 5 results of 5
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1
HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism od Ihn Sik Seong, Elena Ivanova, Jong‐Min Lee, Yeun Su Choo, Elisa Fossale, MaryAnne Anderson, James F. Gusella, Jason M. Laramie, Richard H. Myers, Mathieu Lesort, Marcy E. MacDonald
Izdano 2005Artigo -
2
Normal and Expanded Huntington’s Disease Gene Alleles Produce Distinguishable Proteins Due to Translation Across the CAG Repeat od Francesca Persichetti, Christine Ambrose, Pei Ge, Sandra McNeil, Jayalakshmi Srinidhi, Mary Anne Anderson, Barbara Jenkins, Glenn T. Barnes, Mabel P. Duyao, Lisa Kanaley, Nancy S. Wexler, Richard H. Myers, Edward D. Bird, Jean‐Paul Vonsattel, Marcy E. MacDonald, James F. Gusella, Stuart H. Orkin
Izdano 1995Artigo -
3
Homozygotes for Huntington's disease od Nancy S. Wexler, Anne B. Young, Rudolph E. Tanzi, Helen Travers, Simon Starosta‐Rubinstein, John B. Penney, S. Robert Snodgrass, Ira Shoulson, Fidela Gomez, María Antonia Ramos Arroyo, Graciela K. Penchaszadeh, Humberto Moreno, Kerin Gibbons, A.G. Faryniarz, Wendy Hobbs, Mary Anne Anderson, Ernesto Bonilla, P. Michael Conneally, James F. Gusella
Izdano 1987Artigo -
4
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes od Marcy E. MacDonald, Christine Ambrose, Mabel P. Duyao, Richard H. Myers, Carol Sze Ki Lin, Lakshmi Srinidhi, Glenn Barnes, Sherryl A. Taylor, Marianne F. James, Nicolet Groot, H MacFarlane, Barbara Jenkins, Mary Anne Anderson, Nancy S. Wexler, James F. Gusella, Gillian P. Bates, Sarah Baxendale, Holger Hummerich, Susan Kirby, Mike North, S Youngman, Richard Mott, Günther Zehetner, Zdeněk Sedláček, Annemarie Poustka, Anna‐Maria Frischauf, Hans Lehrach, Alan Buckler, Deanna M. Church, Lynn Doucette‐Stamm, Michael O’Donovan, Laura Riba-Ramírez, Manish A. Shah, Vincent P. Stanton, Scott A. Strobel, K. M. Draths, Jennifer L. Wales, Peter B. Dervan, David E. Housman, Michael R. Altherr, Rita Shiang, Leslie M. Thompson, Thomas J. Fielder, John J. Wasmuth, Danilo A. Tagle, John Valdes, Lawrence Elmer, Marc W. Allard, Lucio H. Castilla, Manju Swaroop, K Blanchard, Francis S. Collins, Russell G. Snell, Tracey Holloway, Kathleen M. Gillespie, Nicole A. Datson, Duncan Shaw, Peter S. Harper
Izdano 1993Artigo -
5
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies od Claire Redin, Harrison Brand, Ryan L. Collins, Tammy Kammin, Elyse Mitchell, Jennelle C. Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M. Seabra, Mary‐Alice Abbott, Omar Abdul‐Rahman, Erika Aberg, Rhett Adley, Sofía Lizeth Alcaráz‐Estrada, Fowzan S. Alkuraya, Yu An, MaryAnne Anderson, Caroline Antolik, Kwame Anyane‐Yeboa, Joan Atkin, Tina M. Bartell, Jonathan A. Bernstein, Elizabeth Beyer, Ian Blumenthal, Ernie M.H.F. Bongers, Eva H. Brilstra, Chester Brown, Hennie T. Brüggenwirth, Bert Callewaert, Colby Chiang, Ken Corning, Helen Cox, Edwin Cuppen, Benjamin Currall, Tom Cushing, D. David, Matthew A. Deardorff, Annelies Dheedene, Marc D’Hooghe, Bert B.A. de Vries, Dawn Earl, Heather Ferguson, Heather Fisher, David Fitzpatrick, Pamela Gerrol, Daniela Giachino, Joseph Glessner, Troy J. Gliem, Margo Grady, Brett H. Graham, Cristin Griffis, Karen W. Gripp, Andrea Gropman, Andrea Hanson‐Kahn, David J. Harris, Mark A. Hayden, R. Sean Hill, Ron Hochstenbach, Jodi D. Hoffman, Robert J. Hopkin, Monika Weisz Hubshman, A. Micheil Innes, Mira Irons, Melita Irving, Jessie C. Jacobsen, Sandra Janssens, Tamison Jewett, John P. Johnson, Marjolijn C.J. Jongmans, Stephen G. Kahler, David A. Koolen, Jerome Korzelius, Peter M. Kroisel, Yves Lacassie, William Lawless, Emmanuelle Lemyre, Kathleen A. Leppig, Alex V. Levin, Haibo Li, Hong Li, Eric C. Liao, Cynthia Lim, Edward J. Lose, Diane Lucente, Michael J. Macera, Poornima Manavalan, Giorgia Mandrile, Carlo Marcelis, Lauren Margolin, Tamara Mason, Diane Masser‐Frye, Michael McClellan, Cinthya J. Zepeda Mendoza, Björn Menten, Sjors Middelkamp, Liya Regina Mikami, Emily Moe, Shehla Mohammed, Tarja Mononen, Megan Mortenson
Izdano 2016Artigo
Iskalna orodja:
Sorodne teme
Biology
Gene
Genetics
Allele
Disease
Huntington's disease
Medicine
Mutant
Trinucleotide repeat expansion
Gene expression
Huntingtin
Huntingtin Protein
Locus (genetics)
Molecular biology
Pathology
Phenotype
Polyglutamine tract
Abnormality
Breakpoint
Cell biology
Chromosome
Coding region
Compound heterozygosity
Computational biology
Copy-number variation
Dominance (genetics)
Exon
Gene product
Genome
Haplotype