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Neurology
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Gene expression studies

Citations 21-30 of 35 total displayed.

Past content (since Oct 2002):

CLINICAL/SCIENTIFIC NOTES
MUTATIONS IN VAPB ARE NOT ASSOCIATED WITH SPORADIC ALS
J. Kirby, C.A.A. Hewamadduma, J. A. Hartley, H. C. Nixon, H. Evans, R. R. Wadhwa, C. Kershaw, P. G. Ince, and P. J. Shaw
Neurology 2007; 68: 1951-1953. [Full text] [PDF]  

ARTICLES
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
H. Engels, A. Brockschmidt, A. Hoischen, C. Landwehr, K. Bosse, C. Walldorf, G. Toedt, B. Radlwimmer, P. Propping, P. Lichter, and R. G. Weber
Neurology 2007; 68: 743-750. [Abstract] [Full text] [PDF]  

EDITORIALS
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
Steven A. Greenberg and George W. Padberg
Neurology 2007; 68: 544-545. [Full text] [PDF]  

ARTICLES
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
R. J. Osborne, S. Welle, S. L. Venance, C. A. Thornton, and R. Tawil
Neurology 2007; 68: 569-577. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Diminished somatostatin gene expression in individuals with HIV and major depressive disorder
I. P. Everall, S. Salaria, J. H. Atkinson, C. Young, J. Corbeil, I. Grant, E. Masliah, and from the HNRC
Neurology 2006; 67: 1867-1869. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Multiplex analysis of expression of three IFNß-induced genes in antibody-positive MS patients
Andrew R. Pachner, Kavitha Narayan, and Elena Pak
Neurology 2006; 66: 444-446. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Matrilin-2 expression distinguishes clinically relevant subsets of pilocytic astrocytoma
M. K. Sharma, M. A. Watson, M. Lyman, A. Perry, K. D. Aldape, F. Deák, and D. H. Gutmann
Neurology 2006; 66: 127-130. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies
E. H. Sherr, R. Owen, D. G. Albertson, D. Pinkel, P. D. Cotter, A. M. Slavotinek, S. W. Hetts, R. J. Jeremy, G. Schilmoeller, K. Schilmoeller, M. Wakahiro, and A. J. Barkovich
Neurology 2005; 65: 1496-1498. [Abstract] [Full text] [PDF]  

ARTICLES
Expression of protein kinase C isoforms and interleukin-1ß in myofibrillar myopathy
G. Vattemi, P. Tonin, M. Mora, M. Filosto, L. Morandi, C. Savio, I. Dal Pra, N. Rizzuto, and G. Tomelleri
Neurology 2004; 62: 1778-1782. [Abstract] [Full text] [PDF]  

ARTICLES
Large-scale disruption of microtubule pathways in morphologically normal human spastin muscle
A. Molon, S. Di Giovanni, Y. W. Chen, P. M. Clarkson, C. Angelini, E. Pegoraro, and E. P. Hoffman
Neurology 2004; 62: 1097-1104. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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