J. Cooper

发表

Interference by Huntingtin and Atrophin-1 with CBP-Mediated Transcription Leading to Cellular Toxicity

C A Ross, C. Ross, S. Tsuji, 2001, Science.

Polyglutamine pathogenesis.

D. Borchelt, C. Ross, R. Margolis, 1999, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Inducible PC12 cell model of Huntington's disease shows toxicity and decreased histone acetylation

C. Ross, A. Sawa, M. F. Peters, 2003, Neuroreport.

Polyglutamine Repeat Length-Dependent Proteolysis of Huntingtin

C. Ross, W. Richards, G. Bitan, 2002, Neurobiology of Disease.

Title Polyglutamine repeat length-dependent proteolysis of huntingtin Permalink

C. Ross, W. Richards, G. Bitan, 2002 .

Corrigendum: Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin (Human Molecular Genetics (1999) 8 (397-407))

D. Borchelt, D. Price, C. Ross, 1999 .

Loss of MiR-7 regulation leads to α-synuclein accumulation and 1 dopaminergic neuronal loss in vivo.

J. Cooper, M. Caldwell, M. O'Neill, 2017 .

Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization

S. Snyder, C. Ross, A. Sawa, 1999, Nature Medicine.

Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture.

C A Ross, D. Borchelt, C. Ross, 1998, Human molecular genetics.

Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin.

D. Borchelt, D. Price, C. Ross, 1999, Human molecular genetics.

Huntingtin-associated protein 1 (HAP1) binds to a Trio-like polypeptide, with a rac1 guanine nucleotide exchange factor domain.

P. Worley, C. Ross, G. Lyford, 1997, Human molecular genetics.

Characterization of Huntingtin Pathologic Fragments in Human Huntington Disease, Transgenic Mice, and Cell Models

D. Borchelt, C. Ross, Andrew T. N. Tebbenkamp, 2007, Journal of neuropathology and experimental neurology.

Wild-Type Huntingtin Protects from Apoptosis Upstream of Caspase-3

A. Hackam, M. Hayden, E. Clementi, 2000, The Journal of Neuroscience.

Nuclear Accumulation of Truncated Atrophin-1 Fragments in a Transgenic Mouse Model of DRPLA

D. Borchelt, D. Price, C. Ross, 1999, Neuron.

Pathogenesis of neurodegenerative diseases associated with expanded glutamine repeats: new answers, new questions.

C. Ross, R. Margolis, A. Sharp, 1998, Progress in brain research.

Nuclear Targeting of Mutant Huntingtin Increases Toxicity

C. Ross, T. Dawson, V. Dawson, 1999, Molecular and Cellular Neuroscience.