Polyglutamine repeats in neurodegenerative diseases

AP Lieberman, VG Shakkottai… - Annual Review of …, 2019 - annualreviews.org
Among the age-dependent protein aggregation disorders, nine neurodegenerative diseases
are caused by expansions of CAG repeats encoding polyglutamine (polyQ) tracts. We …

Curcumin, gut microbiota, and neuroprotection

F Di Meo, S Margarucci, U Galderisi, S Crispi, G Peluso - Nutrients, 2019 - mdpi.com
Curcumin, a nontoxic, naturally occurring polyphenol, has been recently proposed for the
management of neurodegenerative and neurological diseases. However, a discrepancy …

Metabotropic glutamate receptors and neurodegenerative diseases

FM Ribeiro, LB Vieira, RGW Pires, RP Olmo… - Pharmacological …, 2017 - Elsevier
Glutamate is the most important excitatory neurotransmitter of the mammalian central
nervous system (CNS), playing an important role in memory, synaptic plasticity and neuronal …

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

L Mangiarini, K Sathasivam, M Seller, B Cozens… - Cell, 1996 - cell.com
Huntington's disease (HD) is one of an increasing number of neurodegenerative disorders
caused by a CAG/polyglutamine repeat expansion. Mice have been generated that are …

Use of Caenorhabditis elegans as a model to study Alzheimer's disease and other neurodegenerative diseases

AG Alexander, V Marfil, C Li - Frontiers in genetics, 2014 - frontiersin.org
Advances in research and technology has increased our quality of life, allowed us to combat
diseases, and achieve increased longevity. Unfortunately, increased longevity is …

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32. 1

Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa… - Nature …, 1994 - nature.com
We have identified a novel gene containing CAG repeats and mapped it to chromosome
14q32. 1, the genetic locus for Machado-Joseph disease (MJD). In normal individuals the …

Trinucleotide repeat disorders

HT Orr, HY Zoghbi - Annu. Rev. Neurosci., 2007 - annualreviews.org
The discovery that expansion of unstable repeats can cause a variety of neurological
disorders has changed the landscape of disease-oriented research for several forms of …

Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

J Nasir, SB Floresco, JR O'Kusky, VM Diewert… - Cell, 1995 - cell.com
Targeted Disruption of the Huntington's Disease Gene Results in Embryonic Lethality and
Behavioral and Morphological Changes in Page 1 Cell, Vol. 81,811-823, June 2, 1995 …

Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia

SE Browne, AC Bowling, U Macgarvey… - Annals of Neurology …, 1997 - Wiley Online Library
The etiology of the selective neuronal death that occurs in Huntington's disease (HD) is
unknown. Several lines of evidence implicate the involvement of energetic defects and …

Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

S Zeitlin, JP Liu, DL Chapman, VE Papaioannou… - Nature …, 1995 - nature.com
The expansion of GAG triplet repeats in the translated region of the human HD gene,
encoding a protein (huntingtin) of unknown function, is a dominant mutation leading to …