Resultats de la cerca - Jolene R. Guide
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1
Msh2 Acts in Medium-Spiny Striatal Neurons as an Enhancer of CAG Instability and Mutant Huntingtin Phenotypes in Huntington’s Disease Knock-In Mice per Marina Kovalenko, Ella Dragileva, Jason St. Claire, Tammy Gillis, Jolene R. Guide, Jaclyn New, Hualing Dong, Raju Kucherlapati, Melanie H. Kucherlapati, Michelle E. Ehrlich, Jong‐Min Lee, Vanessa C. Wheeler
Publicat 2012Artigo -
2
Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families per Ian Blumenthal, Ashok Ragavendran, Serkan Erdin, Lambertus Klei, Aarathi Sugathan, Jolene R. Guide, Poornima Manavalan, Julian Q. Zhou, Vanessa C. Wheeler, Joshua Z. Levin, Carl Ernst, Kathryn Roeder, Bernie Devlin, James F. Gusella, Michael E. Talkowski
Publicat 2014Artigo -
3
Mismatch Repair Genes Mlh1 and Mlh3 Modify CAG Instability in Huntington's Disease Mice: Genome-Wide and Candidate Approaches per Ricardo Mouro Pinto, Ella Dragileva, Andrew Kirby, Alejandro Lloret, Edith Lopez, Jason St. Claire, Gagan B. Panigrahi, Caixia Hou, Kim Holloway, Tammy Gillis, Jolene R. Guide, Paula E. Cohen, Guo‐Min Li, Christopher E. Pearson, Mark J. Daly, Vanessa C. Wheeler
Publicat 2013Artigo -
4
Large-Scale Phenotyping of an Accurate Genetic Mouse Model of JNCL Identifies Novel Early Pathology Outside the Central Nervous System per John F. Staropoli, Larissa A. Haliw, Sunita Biswas, Lillian Garrett, Sabine M. Hölter, Lore Becker, Sergej Skosyrski, Patricia da Silva‐Buttkus, Julia Calzada‐Wack, Frauke Neff, Birgit Rathkolb, Jan Rozman, Anja Schrewe, Thure Adler, Oliver Puk, Minxuan Sun, Jack Favor, Ildikó Rácz, Raffi Bekeredjian, Dirk H. Busch, Jochen Graw, Martin Klingenspor, Thomas Klopstock, Eckhard Wolf, Wolfgang Wurst, Andreas Zimmer, Edith Lopez, Hayat Harati, Eric Hill, Daniela S. Krause, Jolene R. Guide, Ella Dragileva, Evan Gale, Vanessa C. Wheeler, Rose‐Mary Boustany, Diane E. Brown, Sylvie Breton, Klaus Rüether, Valérie Gailus‐Durner, Helmut Fuchs, Martin Hrabě de Angelis, Susan L. Cotman
Publicat 2012Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Allele
DNA mismatch repair
DNA repair
Disease
Huntingtin
Internal medicine
MSH2
Medicine
Mutant
Trinucleotide repeat expansion
Autism
Cell biology
Congenic
Copy-number variation
Cre recombinase
Developmental psychology
Endocrinology
Ferritin
Gene duplication
Genetically modified mouse
Genome
Hematocrit
Huntingtin Protein
Huntington's disease
Locus (genetics)
MLH1
Mean corpuscular volume