User profiles for "author:Margolis RL"

Robert L Margolis

Professor, Tumor Initiation and Maintenance Program, Sanford-Burnham-Prebys Medical�…
Verified email at SBPdiscovery.org
Cited by 13947

Huntington disease: natural history, biomarkers and prospects for therapeutics

CA Ross, EH Aylward, EJ Wild, DR Langbehn…�- Nature Reviews�…, 2014 - nature.com
Huntington disease (HD) can be seen as a model neurodegenerative disorder, in that it is
caused by a single genetic mutation and is amenable to predictive genetic testing, with�…

[HTML][HTML] Neurobiology of schizophrenia

CA Ross, RL Margolis, SAJ Reading, M Pletnikov…�- Neuron, 2006 - cell.com
With its hallucinations, delusions, thought disorder, and cognitive deficits, schizophrenia
affects the most basic human processes of perception, emotion, and judgment. Evidence�…

G1 tetraploidy checkpoint and the suppression of tumorigenesis

RL Margolis, OD Lohez…�- Journal of cellular�…, 2003 - Wiley Online Library
Checkpoints suppress improper cell cycle progression to ensure that cells maintain the
integrity of their genome. During mitosis, a metaphase checkpoint requires the integration of�…

Opposite end assembly and disassembly of microtubules at steady state in vitro

RL Margolis, L Wilson�- Cell, 1978 - cell.com
Measurements of tubulin exchange into and from bovine brain microtubules at steady state
in vitro were made with 3H-GTP as a marker for tubulin addition to or loss from microtubules�…

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

SE Holmes, EE O'Hearn, MG McInnis…�- Nature�…, 1999 - nature.com
The genetic aetiologies of at least 20% of autosomal dominant spinocerebellar ataxias
(SCAs) have yet to be elucidated 1. We have recently identified a novel form of autosomal�…

Distinct specificity in the recognition of phosphoinositides by the pleckstrin homology domains of dynamin and Bruton's tyrosine kinase.

K Salim, MJ Bottomley, E Querfurth, MJ Zvelebil…�- The EMBO�…, 1996 - embopress.org
Pleckstrin homology (PH) domains may act as membrane localization modules through
specific interactions with phosphoinositide phospholipids. These interactions could�…

A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion

RL Margolis, E O'Hearn, A Rosenblatt…�- Annals of Neurology�…, 2001 - Wiley Online Library
Huntington's disease (HD) is an autosomal dominant disorder characterized by
abnormalities of movement, cognition, and emotion and selective atrophy of the striatum and�…

[HTML][HTML] Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract

CL Wellington, LM Ellerby, AS Hackam…�- Journal of Biological�…, 1998 - ASBMB
The neurodegenerative diseases Huntington disease, dentatorubropallidoluysian atrophy,
spinocerebellar atrophy type 3, and spinal bulbar muscular atrophy are caused by�…

Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions

S Engelender, Z Kaminsky, X Guo, AH Sharp…�- Nature�…, 1999 - nature.com
Parkinson disease (PD) is a neurodegenerative disease characterized by tremor,
bradykinesia, rigidity and postural instability. Post-mortem examination shows loss of�…

Tetraploid state induces p53-dependent arrest of nontransformed mammalian cells in G1

PR Andreassen, OD Lohez, FB Lacroix…�- Molecular biology of�…, 2001 - Am Soc Cell Biol
A “spindle assembly” checkpoint has been described that arrests cells in G1 following
inappropriate exit from mitosis in the presence of microtubule inhibitors. We have here�…