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Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosage

Author
KUHN, Alexandre1 2 ; GOLDSTEIN, Darlene R1 ; HANNAN, Anthony J10 9 ; HAYDEN, Michael R6 ; LEAVITT, Blair R6 ; DUNNETT, Stephen B3 ; FERRANTE, Robert J11 ; ALBIN, Roger12 ; SHELBOURNE, Peggy13 ; DELORENZI, Mauro2 ; AUGOOD, Sarah J8 ; FAULL, Richard L. M14 ; HODGES, Angela3 4 ; OLSON, James M5 ; BATES, Gillian P7 ; JONES, Lesley3 ; LUTHI-CARTER, Ruth1 ; STRAND, Andrew D5 ; SENGSTAG, Thierry2 ; KOOPERBERG, Charles5 ; BECANOVIC, Kristina6 ; POULADI, Mahmoud A6 ; SATHASIVAM, Kirupa7 ; CHA, Jang-Ho J8
[1] Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland
[2] National Center of Competence in Research (NCCR) Molecular Oncology, Swiss Institute of Experimental Cancer Research (ISREC) and Swiss Institute of Bioinformatics (SIB), 1066 Epalinges, Switzerland
[3] Departments of Psychological Medicine and Medical Genetics, Wales College of Medicine and School of Biosciences, Cardiff University, Heath Park, Cardiff CF14 4XN, Wales, United Kingdom
[4] Department of Psychological Medicine, Institute of Psychiatry, King's College London, London SE5 8AF, United Kingdom
[5] Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States
[6] Department of Medical Genetics, University of British Columbia, and Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, Vancouver, BC, V5Z 4H4, Canada
[7] Department of Medical and Molecular Genetics, King's College London School of Medicine, London SE1 9RT, United Kingdom
[8] MassGeneral Institute of Neurodegenerative Disease (MIND), Massachusetts General Hospital, Charlestown, MA 02129, United States
[9] University Laboratory of Physiology, Oxford OX1 3PT, United Kingdom
[10] Howard Florey Institute, National Neuroscience Facility, University of Melbourne, VIC 3010, Australia
[11] Bedford Veterans Affairs Medical Center and Departments of Neurology, Pathology, Psychiatry, Boston University School of Medicine, Bedford, MA 07130, United States
[12] Geriatrics Research, Education, and Clinical Center, Ann Arbor Veterans Affairs Medical Center and Department of Neurology, University of Michigan, United States
[13] Division of Molecular Genetics, Faculty of Biomedical and Life Sciences, University of Glasgow, Glasgow G11 6NU, Scotland, United Kingdom
[14] Department of Anatomy with Radiology, University of Auckland, Private Bag 92019, Auckland, New Zealand
Source

Human molecular genetics (Print). 2007, Vol 16, Num 15, pp 1845-1861, 17 p ; ref : 57 ref

ISSN
0964-6906
Scientific domain
Genetics
Publisher
Oxford University Press, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Chorée Huntington Encéphale pathologie Expression génique Génétique Homme Huntingtine Mutation Souris Extrapyramidal syndrome Maladie dégénérative Maladie héréditaire Mammalia Rodentia Système nerveux central pathologie Système nerveux pathologie Vertebrata
Keyword (en)
Huntington disease Cerebral disorder Gene expression Genetics Human Huntingtin Mutation Mouse Extrapyramidal syndrome Degenerative disease Genetic disease Mammalia Rodentia Central nervous system disease Nervous system diseases Vertebrata
Keyword (es)
Corea Huntington Encéfalo patología Expresión genética Genética Hombre Huntingtina Mutación Ratón Extrapiramidal síndrome Enfermedad degenerativa Enfermedad hereditaria Mammalia Rodentia Sistema nervosio central patología Sistema nervioso patología Vertebrata
Classification
Pascal
002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A04 Molecular and cellular biology

Pascal
002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases

Discipline
Eukaryotes genetics. Biological and molecular evolution Molecular and cell biology Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
19031190

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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