[HTML][HTML] Neurodegenerative diseases–is metabolic deficiency the root cause?
VR Muddapu, SAP Dharshini… - Frontiers in …, 2020 - frontiersin.org
Neurodegenerative diseases, including Alzheimer, Parkinson, Huntington, and amyotrophic
lateral sclerosis, are a prominent class of neurological diseases currently without a cure …
lateral sclerosis, are a prominent class of neurological diseases currently without a cure …
Huntington's disease: mechanisms of pathogenesis and therapeutic strategies
M Jimenez-Sanchez, F Licitra… - Cold Spring …, 2017 - perspectivesinmedicine.cshlp.org
Huntington's disease is a late-onset neurodegenerative disease caused by a CAG
trinucleotide repeat in the gene encoding the huntingtin protein. Despite its well-defined …
trinucleotide repeat in the gene encoding the huntingtin protein. Despite its well-defined …
[HTML][HTML] Cell type-specific transcriptomics reveals that mutant huntingtin leads to mitochondrial RNA release and neuronal innate immune activation
The mechanisms by which mutant huntingtin (mHTT) leads to neuronal cell death in
Huntington's disease (HD) are not fully understood. To gain new molecular insights, we …
Huntington's disease (HD) are not fully understood. To gain new molecular insights, we …
[HTML][HTML] The neuroprotective effects of fisetin, a natural flavonoid in neurodegenerative diseases: Focus on the role of oxidative stress
Oxidative stress (OS) disrupts the chemical integrity of macromolecules and increases the
risk of neurodegenerative diseases. Fisetin is a flavonoid that exhibits potent antioxidant …
risk of neurodegenerative diseases. Fisetin is a flavonoid that exhibits potent antioxidant …
Molecular mechanisms and potential therapeutical targets in Huntington's disease
C Zuccato, M Valenza, E Cattaneo - Physiological reviews, 2010 - journals.physiology.org
Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG repeat
expansion in the gene encoding for huntingtin protein. A lot has been learned about this …
expansion in the gene encoding for huntingtin protein. A lot has been learned about this …
Enriched environments, experience-dependent plasticity and disorders of the nervous system
J Nithianantharajah, AJ Hannan - Nature Reviews Neuroscience, 2006 - nature.com
Behavioural, cellular and molecular studies have revealed significant effects of enriched
environments on rodents and other species, and provided new insights into mechanisms of …
environments on rodents and other species, and provided new insights into mechanisms of …
[HTML][HTML] Comprehensive behavioral and molecular characterization of a new knock-in mouse model of Huntington's disease: zQ175
LB Menalled, AE Kudwa, S Miller, J Fitzpatrick… - PloS one, 2012 - journals.plos.org
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder
characterized by motor, cognitive and psychiatric manifestations. Since the mutation …
characterized by motor, cognitive and psychiatric manifestations. Since the mutation …
[HTML][HTML] Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes
Hd iPsc Consortium - Cell stem cell, 2012 - cell.com
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an
expanded stretch of CAG trinucleotide repeats that results in neuronal dysfunction and …
expanded stretch of CAG trinucleotide repeats that results in neuronal dysfunction and …
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
C Zuccato, A Ciammola, D Rigamonti, BR Leavitt… - Science, 2001 - science.org
Huntingtin is a 350-kilodalton protein of unknown function that is mutated in Huntington's
disease (HD), a neurodegenerative disorder. The mutant protein is presumed to acquire a …
disease (HD), a neurodegenerative disorder. The mutant protein is presumed to acquire a …
Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines
AV Panov, CA Gutekunst, BR Leavitt, MR Hayden… - Nature …, 2002 - nature.com
Huntington's disease (HD) is caused by an expansion of exonic CAG triplet repeats in the
gene encoding huntingtin protein (Htt), but the mechanisms by which this mutant protein …
gene encoding huntingtin protein (Htt), but the mechanisms by which this mutant protein …