Specific splice variants are associated with Parkinson's disease-Reference-Cited by-同舟云学术

Specific splice variants are associated with Parkinson's disease

Published:2013-09-20 Issue:12 Volume:28 Page:1724-1727
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Santiago Jose A.¹,Scherzer Clemens R.²,Potashkin Judith A.¹²,

Affiliation:

1. Department of Cellular and Molecular Pharmacology; The Chicago Medical School; Rosalind Franklin University of Medicine and Science; North Chicago Illinois USA

2. The Neurogenomics Laboratory; Harvard Medical School and Brigham and Women's Hospital; Cambridge Massachusetts USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference12 articles.

1. Molecular markers of early Parkinson's disease based on gene expression in blood;Scherzer;Proc Natl Acad Sci U S A,2007

2. A molecular signature in blood identifies early Parkinson's disease;Molochnikov;Mol Neurodegener,2012

3. Exon arrays reveal alternative splicing aberrations in Parkinson's disease leukocytes;Soreq;Neurodegener Dis,2012

4. Biosignatures for Parkinson's disease and atypical parkinsonian disorders patients;Potashkin;PloS One,2012

5. Association of SNCA with Parkinson: replication in the Harvard NeuroDiscovery Center Biomarker Study;Ding;Mov Disord,2011

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