Literature DB >> 1827708

Molecular approaches to hereditary diseases of the nervous system: Huntington's disease as a paradigm.

N S Wexler1, E A Rose, D E Housman.   

Abstract

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Year:  1991        PMID： 1827708     DOI： 10.1146/annurev.ne.14.030191.002443

Source DB:  PubMed          Journal:  Annu Rev Neurosci        ISSN： 0147-006X            Impact factor:   12.449


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  16 in total

1.  Primary structure, chromosomal localization, and functional expression of a voltage-gated sodium channel from human brain.

Authors:  C M Ahmed; D H Ware; S C Lee; C D Patten; A V Ferrer-Montiel; A F Schinder; J D McPherson; C B Wagner-McPherson; J J Wasmuth; G A Evans
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-01       Impact factor: 11.205

2.  Testing for Huntington's disease.

Authors:  R Williamson
Journal:  BMJ       Date:  1992-06-20

Review 3.  Molecular biology of neurological diseases.

Authors:  W J Cumming
Journal:  Postgrad Med J       Date:  1992-04       Impact factor: 2.401

Review 4.  Dopamine receptor genes: new tools for molecular psychiatry.

Authors:  H B Niznik; H H Van Tol
Journal:  J Psychiatry Neurosci       Date:  1992-10       Impact factor: 6.186

5.  Molecular cloning, chromosomal mapping, and functional expression of human brain glutamate receptors.

Authors:  W Sun; A V Ferrer-Montiel; A F Schinder; J P McPherson; G A Evans; M Montal
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

Review 6.  The elimination of accumulated and aggregated proteins: a role for aggrephagy in neurodegeneration.

Authors:  Ai Yamamoto; Anne Simonsen
Journal:  Neurobiol Dis       Date:  2010-08-20       Impact factor: 5.996

Review 7.  The paradigm of Huntington's disease: therapeutic opportunities in neurodegeneration.

Authors:  Julie Leegwater-Kim; Jang-Ho J Cha
Journal:  NeuroRx       Date:  2004-01

8.  Synchrotron infrared microspectroscopy detecting the evolution of Huntington's disease neuropathology and suggesting unique correlates of dysfunction in white versus gray brain matter.

Authors:  Markus Bonda; Valérie Perrin; Bertrand Vileno; Heike Runne; Ariane Kretlow; László Forró; Ruth Luthi-Carter; Lisa M Miller; Sylvia Jeney
Journal:  Anal Chem       Date:  2011-09-22       Impact factor: 6.986

9.  A large number of protein expression changes occur early in life and precede phenotype onset in a mouse model for huntington disease.

Authors:  Claus Zabel; Lei Mao; Ben Woodman; Michael Rohe; Maik A Wacker; Yvonne Kläre; Andrea Koppelstätter; Grit Nebrich; Oliver Klein; Susanne Grams; Andrew Strand; Ruth Luthi-Carter; Daniela Hartl; Joachim Klose; Gillian P Bates
Journal:  Mol Cell Proteomics       Date:  2008-11-30       Impact factor: 5.911

10.  Factors associated with HD CAG repeat instability in Huntington disease.

Authors:  V C Wheeler; F Persichetti; S M McNeil; J S Mysore; S S Mysore; M E MacDonald; R H Myers; J F Gusella; N S Wexler
Journal:  J Med Genet       Date:  2007-07-27       Impact factor: 6.318
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