Literature DB >> 15018843

Mutant genes responsible for Parkinson's disease.

Weidong Le1, Stanley H Appel.   

Abstract

Recent progress has documented the presence of at least 10 disease-related genes or loci linked to Parkinson's disease. Analysis of the genotypes and phenotypes of these mutant genes has revealed a broad spectrum of clinical and pathological presentations, many of which share a common feature of alteration in the ubiquitin proteasome system. Further understanding of the pathogenesis of these inherited cases of Parkinson's disease and development of transgenic animal models bearing these mutations should provide novel insight into the causes of nigral cell death and meaningful strategies for future therapy.

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Year:  2004        PMID: 15018843     DOI: 10.1016/j.coph.2003.09.005

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  6 in total

Review 1.  Ubiquitin-proteasome system as a modulator of cell fate.

Authors:  Simon J Thompson; Liam T Loftus; Michelle D Ashley; Robert Meller
Journal:  Curr Opin Pharmacol       Date:  2007-11-05       Impact factor: 5.547

Review 2.  Neuroproteomics as a promising tool in Parkinson's disease research.

Authors:  Ilse S Pienaar; William M U Daniels; Jürgen Götz
Journal:  J Neural Transm (Vienna)       Date:  2008-06-04       Impact factor: 3.575

Review 3.  Dealing with misfolded proteins: examining the neuroprotective role of molecular chaperones in neurodegeneration.

Authors:  Yousuf O Ali; Brandon M Kitay; R Grace Zhai
Journal:  Molecules       Date:  2010-10-08       Impact factor: 4.411

Review 4.  Are heat shock proteins therapeutic target for Parkinson's disease?

Authors:  Guang-Rui Luo; Sheng Chen; Wei-Dong Le
Journal:  Int J Biol Sci       Date:  2006-10-15       Impact factor: 6.580

5.  Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.

Authors:  Balaji S Srinivasan; Jaleh Doostzadeh; Farnaz Absalan; Sharareh Mohandessi; Roxana Jalili; Saharnaz Bigdeli; Justin Wang; Jaydev Mahadevan; Caroline L G Lee; Ronald W Davis; J William Langston; Mostafa Ronaghi
Journal:  Hum Mutat       Date:  2009-02       Impact factor: 4.878

6.  Whole exome sequencing identified a new compound heterozygous PRKN mutation in a Chinese family with early-onset Parkinson's disease.

Authors:  Tianbai Li; Daqing Kou; Yanhua Cui; Weidong Le
Journal:  Biosci Rep       Date:  2020-05-29       Impact factor: 3.840

  6 in total

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