Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders

被引：0

作者：

Mang Ching Lai

Anne-Laure Bechy

Franziska Denk

Emma Collins

Maria Gavriliouk

Judith B. Zaugg

Brent J. Ryan

Richard Wade-Martins

Tara M. Caffrey

机构：

[1] University of Oxford,Department of Physiology, Anatomy and Genetics

[2] European Molecular Biology Laboratory,Oxford Parkinson’s Disease Centre

[3] University of Oxford,undefined

来源：

Molecular Neurodegeneration | / 12卷

关键词：

Tau; Progressive supranuclear palsy; Alzheimer’s disease; Corticobasal degeneration; Parkinson’s disease;

D O I：

暂无

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摘要：

引用

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[1]

Abecasis GR(2012)An integrated map of genetic variation from 1,092 human genomes Nature 491 56-65

[2]

Auton A(2008)Microarray technology and applications in the arena of genome-wide association Clin Chem 54 1116-1124

[3]

Brooks LD(2003)The international HapMap project Nature 426 789-796

[4]

DePristo MA(2001)Initial sequencing and analysis of the human genome Nature 409 860-921

[5]

Durbin RM(2009)Human genetic variation and its contribution to complex traits Nat Rev Genet 10 241-251

[6]

Handsaker RE(2010)A map of human genome variation from population-scale sequencing Nature 467 1061-1073

[7]

Kang HM(2012)Linking disease associations with regulatory information in the human genome Genome Res 22 1748-1759

[8]

Marth GT(2011)Principles for the post-GWAS functional characterization of cancer risk loci Nat Genet 43 513-518

[9]

McVean GA(2012)Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression Nat Genet 44 1191-1198

[10]

Consortium GP(2009)The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer Nat Genet 41 882-884