Literature DB >> 11898503

A molecular basis for hereditary motor and sensory neuropathy disorders.

M E Shy1, J Balsamo, J Lilien, J Kamholz.   

Abstract

Charcot-Marie-Tooth disease (CMT), or inherited peripheral neuropathies, is one of the most frequent genetically inherited neurologic disorders, with a prevalence of approximately one in 2500 people. CMT is usually inherited in an autosomal dominant fashion, although X-linked and recessive forms of CMT also exist. Over the past several years, considerable progress has been made toward understanding the genetic causes of many of the most frequent forms of CMT, particularly those caused by mutations in Schwann cell genes inducing the demyelinating forms of CMT, also known as CMT1. Because the genetic cause of these disorders is known, it is now possible to study how mutations in genes encoding myelin proteins cause neuropathy. Identifying these mechanisms will be important both for understanding demyelination and for developing future treatments for CMT.

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Year:  2001        PMID: 11898503     DOI: 10.1007/s11910-001-0079-6

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  95 in total

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Journal:  Ann Neurol       Date:  1994-09       Impact factor: 10.422

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Journal:  Brain       Date:  1999-08       Impact factor: 13.501

7.  Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele.

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Journal:  J Neurosci Res       Date:  1997-09-15       Impact factor: 4.164

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Journal:  J Cell Biol       Date:  1996-09       Impact factor: 10.539

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Journal:  Nature       Date:  1994-10-27       Impact factor: 49.962

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  7 in total

1.  Rapamycin activates autophagy and improves myelination in explant cultures from neuropathic mice.

Authors:  Sunitha Rangaraju; Jonathan D Verrier; Irina Madorsky; Jessica Nicks; William A Dunn; Lucia Notterpek
Journal:  J Neurosci       Date:  2010-08-25       Impact factor: 6.167

2.  Conduction block in PMP22 deficiency.

Authors:  Yunhong Bai; Xuebao Zhang; Istvan Katona; Mario Andre Saporta; Michael E Shy; Heather A O'Malley; Lori L Isom; Ueli Suter; Jun Li
Journal:  J Neurosci       Date:  2010-01-13       Impact factor: 6.167

3.  Pharmacological induction of the heat shock response improves myelination in a neuropathic model.

Authors:  Sunitha Rangaraju; Irina Madorsky; Jocelyn Go Pileggi; Adeela Kamal; Lucia Notterpek
Journal:  Neurobiol Dis       Date:  2008-07-08       Impact factor: 5.996

4.  Mutations in the cytoplasmic domain of P0 reveal a role for PKC-mediated phosphorylation in adhesion and myelination.

Authors:  W Xu; M Shy; J Kamholz; L Elferink; G Xu; J Lilien; J Balsamo
Journal:  J Cell Biol       Date:  2001-10-22       Impact factor: 10.539

5.  The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease.

Authors:  Axel Niemann; Nina Huber; Konstanze M Wagner; Christian Somandin; Michael Horn; Frédéric Lebrun-Julien; Brigitte Angst; Jorge A Pereira; Hartmut Halfter; Hans Welzl; M Laura Feltri; Lawrence Wrabetz; Peter Young; Carsten Wessig; Klaus V Toyka; Ueli Suter
Journal:  Brain       Date:  2014-01-29       Impact factor: 13.501

6.  Myelin protein zero/P0 phosphorylation and function require an adaptor protein linking it to RACK1 and PKC alpha.

Authors:  Ana-Maria Gaboreanu; Ronald Hrstka; Wenbo Xu; Michael Shy; John Kamholz; Jack Lilien; Janne Balsamo
Journal:  J Cell Biol       Date:  2007-05-14       Impact factor: 10.539

7.  Myelin Pathology: Involvement of Molecular Chaperones and the Promise of Chaperonotherapy.

Authors:  Federica Scalia; Antonella Marino Gammazza; Everly Conway de Macario; Alberto J L Macario; Francesco Cappello
Journal:  Brain Sci       Date:  2019-10-30
  7 in total

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