Literature DB >> 1853757

A candidate gene for X-linked spinal muscular atrophy.

K H Fischbeck1, D Souders, A La Spada.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1991        PMID： 1853757

Source DB:  PubMed          Journal:  Adv Neurol        ISSN： 0091-3952


× No keyword cloud information.
  6 in total

1.  Contractile dysfunction in muscle may underlie androgen-dependent motor dysfunction in spinal bulbar muscular atrophy.

Authors:  Kentaro Oki; Katherine Halievski; Laura Vicente; Youfen Xu; Donald Zeolla; Jessica Poort; Masahisa Katsuno; Hiroaki Adachi; Gen Sobue; Robert W Wiseman; S Marc Breedlove; Cynthia L Jordan
Journal:  J Appl Physiol (1985)       Date:  2015-02-05

Review 2.  Kennedy disease.

Authors:  K H Fischbeck
Journal:  J Inherit Metab Dis       Date:  1997-06       Impact factor: 4.982

3.  Neuromuscular junctions are pathological but not denervated in two mouse models of spinal bulbar muscular atrophy.

Authors:  Jessica E Poort; Mary B Rheuben; S Marc Breedlove; Cynthia L Jordan
Journal:  Hum Mol Genet       Date:  2016-08-04       Impact factor: 6.150

4.  Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases.

Authors:  Wojciech J Szlachcic; Pawel M Switonski; Małgorzata Kurkowiak; Kalina Wiatr; Maciej Figiel
Journal:  Mol Brain       Date:  2015-10-29       Impact factor: 4.041

Review 5.  Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions.

Authors:  April L Darling; Vladimir N Uversky
Journal:  Molecules       Date:  2017-11-24       Impact factor: 4.411

Review 6.  Mouse models of polyglutamine diseases: review and data table. Part I.

Authors:  Maciej Figiel; Wojciech J Szlachcic; Pawel M Switonski; Agnieszka Gabka; Wlodzimierz J Krzyzosiak
Journal:  Mol Neurobiol       Date:  2012-09-07       Impact factor: 5.590
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.