High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington’s disease CAG knock-in mice across multiple genetic backgrounds

Author:

Ament Seth A.12,Pearl Jocelynn R.13,Grindeland Andrea4,St. Claire Jason5,Earls John C.16,Kovalenko Marina5,Gillis Tammy5,Mysore Jayalakshmi5,Gusella James F.5,Lee Jong-Min5,Kwak Seung7,Howland David7,Lee Min Young1,Baxter David1,Scherler Kelsey1,Wang Kai1,Geman Donald8,Carroll Jeffrey B.9,MacDonald Marcy E.5,Carlson George4,Wheeler Vanessa C.5,Price Nathan D.1,Hood Leroy E.1

Affiliation:

1. Institute for Systems Biology, Seattle, WA, USA

2. Institute for Genome Sciences and Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD, USA

3. Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA, USA

4. McLaughlin Research Institute, Great Falls, MT, USA

5. Center for Human Genetic Research, Massachusetts General Hospital, Department of Neurology, Harvard Medical School, Boston, MA, USA

6. Department of Computer Science, University of Washington, Seattle, WA, USA

7. CHDI Management/CHDI Foundation, Princeton, NJ, USA

8. Department of Applied Mathematics and Statistics, Johns Hopkins University, Baltimore, MD, USA

9. Behavioral Neuroscience Program, Department of Psychology, Western Washington University, Bellingham, WA, USA

Funder

NIH

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference47 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes;The Huntington's Disease Collaborative Research Group;Cell,1993

2. Trinucleotide repeat length instability and age of onset in Huntington’s disease;Duyao;Nat. Genet,1993

3. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington’s disease;Andrew;Nat. Genet,1993

4. A new model for prediction of the age of onset and penetrance for Huntington’s disease based on CAG length;Langbehn;Clin. Genet,2004

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