Neuropathology and Genetics of Cerebroretinal Vasculopathies-Reference-Cited by-同舟云学术

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Neuropathology and Genetics of Cerebroretinal Vasculopathies

Published:2014-09 Issue:5 Volume:24 Page:510-518
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Kolar Grant R.¹,Kothari Parul H.²,Khanlou Negar³,Jen Joanna C.⁴,Schmidt Robert E.⁵,Vinters Harry V.³⁴

Affiliation:

1. Department of Pathology; Saint Louis University School of Medicine; St. Louis MO

2. Department of Genetics; Washington University in St. Louis; St. Louis MO

3. Departments of Pathology and Laboratory Medicine (Neuropathology); University of California Los Angeles (UCLA); Los Angeles CA

4. Neurology; David Geffen School of Medicine; Ronald Reagan UCLA Medical Center; University of California Los Angeles (UCLA); Los Angeles CA

5. Division of Neuropathology; Washington University in St. Louis; St. Louis MO

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bpa.12178/fullpdf

Reference30 articles.

1. The exonuclease TREX1 is in the SET complex and acts in concert with NM23-H1 to degrade DNA during granzyme A-mediated cell death;Chowdhury;Mol Cell,2006

2. Novel ophthalmological features in hereditary endotheliopathy with retinopathy, nephropathy and stroke syndrome;Cohn;Clin Experiment Ophthalmol,2005

3. Mutations in the gene encoding the 3“-5” DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus;Crow;Nat Genet,2006

4. TREX2 exonuclease defective cells exhibit double-strand breaks and chromosomal fragments but not Robertsonian translocations;Dumitrache;Mutat Res,2009

5. Cerebroretinal vasculopathy. A new hereditary syndrome;Grand;Ophthalmology,1988

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