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Gene expression studies
Citations 1-10 of 22 total displayed.
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Most recent content
(15 Jul 2008):
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- ARTICLES
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
- B. A. Neubauer, S. Waldegger, J. Heinzinger, A. Hahn, G. Kurlemann, B. Fiedler, F. Eberhard, H. Muhle, U. Stephani, S. Garkisch, O. Eeg-Olofsson, U. Müller, and T. Sander
Neurology 2008; 71: 177-183.
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Past content
(since Oct 2002):
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- EDITORIALS
Association, expression, pathobiology: Is too much tau in PD a blueprint for genetic association?
- Andrew Singleton and Huw Morris
Neurology 2008; 71: 11-12.
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- ARTICLES
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
- J. E. Tobin, J. C. Latourelle, M. F. Lew, C. Klein, O. Suchowersky, H. A. Shill, L. I. Golbe, M. H. Mark, J. H. Growdon, G. F. Wooten, B. A. Racette, J. S. Perlmutter, R. Watts, M. Guttman, K. B. Baker, S. Goldwurm, G. Pezzoli, C. Singer, M. H. Saint-Hilaire, A. E. Hendricks, S. Williamson, M. W. Nagle, J. B. Wilk, T. Massood, J. M. Laramie, A. L. DeStefano, I. Litvan, G. Nicholson, A. Corbett, S. Isaacson, D. J. Burn, P. F. Chinnery, P. P. Pramstaller, S. Sherman, J. Al-hinti, E. Drasby, M. Nance, A. T. Moller, K. Ostergaard, R. Roxburgh, B. Snow, J. T. Slevin, F. Cambi, J. F. Gusella, and R. H. Myers
Neurology 2008; 71: 28-34.
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- ARTICLES
Paraoxonase 1 (PON1) organophosphate hydrolysis is not reduced in ALS
- A. -M. Wills, J. E. Landers, H. Zhang, R. J. Richter, A. J. Caraganis, M. E. Cudkowicz, C. E. Furlong, and R. H. Brown, Jr
Neurology 2008; 70: 929-934.
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- CLINICAL/SCIENTIFIC NOTES
CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA
- T. Obi, K. Nishioka, O. A. Ross, T. Terada, K. Yamazaki, A. Sugiura, M. Takanashi, K. Mizoguchi, H. Mori, Y. Mizuno, and N. Hattori
Neurology 2008; 70: 238-241.
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- VIEWS & REVIEWS
Parkinson disease, 10 years after its genetic revolution: Multiple clues to a complex disorder
- Christine Klein and Michael G. Schlossmacher
Neurology 2007; 69: 2093-2104.
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- ARTICLES
GNE protein expression and subcellular distribution are unaltered in HIBM
- S. Krause, A. Aleo, S. Hinderlich, L. Merlini, I. Tournev, M. C. Walter, Z. Argov, S. Mitrani-Rosenbaum, and H. Lochmüller
Neurology 2007; 69: 655-659.
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- 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.
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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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