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A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

Terri G. Thompson
Christine J. DiDonato
John J. Wasmuth
Research01 Jan 1995
Nature Genetics

Volume: 9, P: 56-62
SMN oligomerization defect correlates with spinal muscular atrophy severity

Christian L. Lorson
John Strasswimmer
Elliot J. Androphy
Research01 May 1998
Nature Genetics

Volume: 19, P: 63-66
Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1

Karen Duff
Chris Eckman
Steven Younkin
Research24 Oct 1996
Nature

Volume: 383, P: 710-713
Hypermethylation trigger of the glutathione-S-transferase gene (GSTP1) in prostate cancer cells

Jenny Z Song
Clare Stirzaker
Susan J Clark
Research18 Feb 2002
Oncogene

Volume: 21, P: 1048-1061
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Leonard van den Berg, Roel Ophoff and colleagues present a genome-wide association study of sporadic amyotrophic lateral sclerosis. The work uncovers associated SNPs at 9p21.2 and an associated locus at 19p13.3 mapping to the UNC13A gene.

Michael A van Es
Jan H Veldink
Leonard H van den Berg
Research06 Sept 2009
Nature Genetics

Volume: 41, P: 1083-1087
Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates

Fibrillar polyglutamine aggregates are taken up by mammalian cells in culture and associate with aggresomes that contain both proteasome subunits and chaperones. Aggresomes also recruit soluble proteins that share the same amyloidogenic sequences as the internalised polyglutamine aggregates.

Pei-Hsien Ren
Jane E. Lauckner
Ron R. Kopito
Research18 Jan 2009
Nature Cell Biology

Volume: 11, P: 219-225
Alterations in the p16^INK4a and p53 tumor suppressor genes of hTERT-immortalized human fibroblasts

Jane R Noble
Ze-Huai Zhong
Roger R Reddel
Research26 Jan 2004
Oncogene

Volume: 23, P: 3116-3121

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A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

SMN oligomerization defect correlates with spinal muscular atrophy severity

Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1

Hypermethylation trigger of the glutathione-S-transferase gene (GSTP1) in prostate cancer cells

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates

Alterations in the p16^INK4a and p53 tumor suppressor genes of hTERT-immortalized human fibroblasts

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A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients

SMN oligomerization defect correlates with spinal muscular atrophy severity

Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1

Hypermethylation trigger of the glutathione-S-transferase gene (GSTP1) in prostate cancer cells

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

Cytoplasmic penetration and persistent infection of mammalian cells by polyglutamine aggregates

Alterations in the p16INK4a and p53 tumor suppressor genes of hTERT-immortalized human fibroblasts

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Alterations in the p16^INK4a and p53 tumor suppressor genes of hTERT-immortalized human fibroblasts