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Scholar Results 1 - 10 of about 74 citing Siderowf: Update on Parkinson disease. (0.09 sec) 

Molecular pathways of neurodegeneration in Parkinson's disease

- sciencesignaling.org
TM Dawson, VL Dawson - Science Signaling, 2003 - stkemag.highwire.org
Abstract: Parkinson's disease (PD) is a complex disorder with many different
causes, yet they may intersect in common pathways, raising the possibility that
neuroprotective agents may have broad applicability in the treatment of PD. ...
Cited by 644 - Related articles - BL Direct - All 15 versions

Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: …

- jneurosci.org
KL Lim, K Chew, JMM Tan, C Wang, KKK … - Journal of Neuroscience, 2005 - Soc Neuroscience
It is widely accepted that the familial Parkinson's disease (PD)-linked gene
product, parkin, functions as a ubiquitin ligase involved in protein turnover
via the ubiquitin-proteasome system. Substrates ubiquitinated by parkin are ...
Cited by 109 - Related articles - All 6 versions

Copper homeostasis and neurodegenerative disorders (Alzheimer's, prion, and Parkinson's …

- hamilton.edu [PDF] 
E Gaggelli, H Kozlowski, D Valensin, G … - Chem. Rev, 2006 - pubs.acs.org
Gianni Valensin (born 1946) received his degree in Chemistry from the University
of Florence, Italy, in 1970. He was appointed Full Professor of Physical
Chemistry in 1986 at the University of Basilicata, Italy, and, later, Full ...
Cited by 105 - Related articles - All 8 versions

{alpha}-Synuclein and Parkinson's disease

- fasebj.org
A Recchia, P Debetto, A Negro, D GUIDOLIN … - The FASEB Journal, 2004 - FASEB
Alpha-synuclein ( -syn) is a small soluble protein expressed primarily at
presynaptic terminals in the central nervous system. Interest in -syn has
increased dramatically after the discovery of a relationship between its ...
Cited by 65 - Related articles - BL Direct - All 3 versions

Familial-associated mutations differentially disrupt the solubility, localization, binding and …

- oxfordjournals.org
SR Sriram, X Li, HS Ko, KKK Chung, E Wong … - Human Molecular Genetics, 2005 - Oxford Univ Press
Mutations in parkin are largely associated with autosomal recessive juvenile
parkinsonism. The underlying mechanism of pathogenesis in parkin-associated
Parkinson's disease (PD) is thought to be due to the loss of parkin's E3 ...
Cited by 62 - Related articles - BL Direct - All 7 versions

Early environmental origins of neurodegenerative disease in later life


PJ Landrigan, B Sonawane, RN Butler, L … - Environmental health perspectives, 2005 - pubmedcentral.nih.gov
Parkinson disease (PD) and Alzheimer disease (AD), the two most common
neurodegenerative disorders in American adults, are of purely genetic origin in
a minority of cases and appear in most instances to arise through ...
Cited by 61 - Related articles - BL Direct - All 17 versions

Glutathione depletion resulting in selective mitochondrial complex I inhibition in …


M Hsu, B Srinivas, J Kumar, R Subramanian, … - Journal of neurochemistry, 2005 - interscience.wiley.com
An early biochemical change in the Parkinsonian substantia nigra (SN) is
reduction in total glutathione (GSH + GSSG) levels in affected dopaminergic
neurons prior to depletion in mitochondrial complex I activity, dopamine ...
Cited by 48 - Related articles - All 4 versions

Alterations in the solubility and intracellular localization of parkin by several familial …


C Wang, JMM Tan, MWL Ho, N Zaiden, SH … - Journal of neurochemistry, 2005 - interscience.wiley.com
Mutations in the parkin gene, which encodes a ubiquitin ligase, are currently
recognized as the main contributor to familial forms of Parkinson's disease
(PD). A simple assumption about the effects of PD-linked mutations in ...
Cited by 48 - Related articles - All 5 versions

Gene therapy of the brain: the trans-vascular approach


F Schlachetzki, Y Zhang, RJ Boado, WM … - Neurology, 2004 - AAN Enterprises
Many chronic neurologic diseases do not respond to small molecule therapeutics,
and have no effective long-term therapy. Gene therapy offers the promise of an
effective cure for both genetic and acquired brain disease. However, the ...
Cited by 39 - Related articles - BL Direct - All 4 versions

Neuroprotection by iron chelator against proteasome inhibitor-induced nigral degeneration


X Zhang, W Xie, S Qu, T Pan, X Wang, W Le - Biochemical and Biophysical Research …, 2005 - Elsevier
The cause of the neurodegenerative process in Parkinson's disease (PD) remains
unclear, but evidence suggests that failure of the ubiquitin–proteasome system
may play a major role in the pathogenesis of the disease. Iron is believed ...
Cited by 30 - Related articles - All 4 versions


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