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Gene expression studies
Citations 21-30 of 34 total displayed.
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Past content
(since Oct 2002):
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- 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.
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- EDITORIALS
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
- Steven A. Greenberg and George W. Padberg
Neurology 2007; 68: 544-545.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- 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.
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- BRIEF COMMUNICATIONS
Ullrich disease due to deficiency of collagen VI in the sarcolemma
- H. Ishikawa, K. Sugie, K. Murayama, A. Awaya, Y. Suzuki, S. Noguchi, Y. K. Hayashi, I. Nonaka, and I. Nishino
Neurology 2004; 62: 620-623.
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