Inactivation of the Mouse Huntington's Disease Gene Homolog Hdh-Reference-Cited by-同舟云学术

Inactivation of the Mouse Huntington's Disease Gene Homolog Hdh

Published:1995-07-21 Issue:5222 Volume:269 Page:407-410
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Duyao Mabel P.¹,Auerbach Anna B.²,Ryan Angela¹,Persichetti Francesca¹,Barnes Glenn T.¹,McNeil Sandra M.¹,Ge Pei³,Vonsattel Jean-Paul³,Gusella James F.¹,Joyner Alexandra L.²,MacDonald Marcy E.¹

Affiliation:

1. Molecular Neurogenetics Unit, Massachusetts General Hospital, Charlestown, MA 02129, USA.

2. Division of Molecular and Developmental Biology, Mount Sinai Hospital, Toronto M5G1X5, Canada.

3. Laboratory for Molecular Neuropathology, Massachusetts General Hospital, Charlestown, MA 02129, USA.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference31 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

2. CELL 78: 23 (1994).

3. AMBROSE, C.M., STRUCTURE AND EXPRESSION OF THE HUNTINGTONS-DISEASE GENE - EVIDENCE AGAINST SIMPLE INACTIVATION DUE TO AN EXPANDED CAG REPEAT, SOMATIC CELL AND MOLECULAR GENETICS 20: 27 (1994).

4. BARNES, G.T., MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG (HDH), SOMATIC CELL AND MOLECULAR GENETICS 20: 87 (1994).

5. BLUM, M, GASTRULATION IN THE MOUSE - THE ROLE OF THE HOMEOBOX GENE GOOSECOID, CELL 69: 1097 (1992).

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