Related references
Note: Only part of the references are listed.Abnormal morphology of peripheral cell tissues from patients with Huntington disease
Ferdinando Squitieri et al.
JOURNAL OF NEURAL TRANSMISSION (2010)
DNA instability in replicating Huntington's disease lymphoblasts
Milena Cannella et al.
BMC MEDICAL GENETICS (2009)
Impaired PGC-1α function in muscle in Huntington's disease
Rajnish K. Chaturvedi et al.
HUMAN MOLECULAR GENETICS (2009)
Evidence of apoptosis and mitochondrial abnormalities in peripheral blood cells of Huntington's disease patients
Sandra Almeida et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)
Huntington's disease:: from huntingtin function and dysfunction to therapeutic strategies
M. Borrell-Pages et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2006)
Genotype-dependent priming to self- and xeno-cannibalism in heterozygous and homozygous lymphoblasts from patients with Huntington's disease
Elisabetta Mormone et al.
JOURNAL OF NEUROCHEMISTRY (2006)
Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin
Rona K. Graham et al.
CELL (2006)
Severe ultrastructural mitochondrial changes in lymphoblasts homozygous for Huntington disease mutation
F Squitieri et al.
MECHANISMS OF AGEING AND DEVELOPMENT (2006)
Huntingtin fragmentation and increased caspase 3, 8 and 9 activities in lymphoblasts with heterozygous and homozygous Huntington's disease mutation
V Maglione et al.
MECHANISMS OF AGEING AND DEVELOPMENT (2006)
Expression pattern of apoptosis-related markers in Huntington's disease
JC Vis et al.
ACTA NEUROPATHOLOGICA (2005)
The gender effect in juvenile Huntington disease patients of Italian origin
M Cannella et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2004)
Autophagosome-like vacuole formation in Huntington's disease lymphoblasts
E Nagata et al.
NEUROREPORT (2004)
Huntingtin and its role in neuronal degeneration
SH Li et al.
NEUROSCIENTIST (2004)
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
F Squitieri et al.
BRAIN (2003)
Comparison of huntingtin proteolytic fragments in human lymphoblast cell lines and human brain
T Toneff et al.
JOURNAL OF NEUROCHEMISTRY (2002)
Loss of normal huntingtin function: new developments in Huntington's disease research
E Cattaneo et al.
TRENDS IN NEUROSCIENCES (2001)
Wild-type huntingtin reduces the cellular toxicity of mutant huntingtin in vivo
BR Leavitt et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Mutant huntingtin enhances excitotoxic cell death
MM Zeron et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2001)
Minocycline inhibits caspase-1 and caspase-3 expression and delays mortality in a transgenic mouse model of Huntington disease
M Chen et al.
NATURE MEDICINE (2000)
Inhibiting caspase cleavage of huntingtin reduces toxicity and aggregate formation in neuronal and nonneuronal cells
CL Wellington et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Share Paper
