Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1 (English)
- New search for: Watase, Kei
- New search for: Venken, Koen J. T.
- New search for: Sun, Yaling
- New search for: Orr, Harry T.
- New search for: Zoghbi, Huda Y.
- New search for: Watase, Kei
- New search for: Venken, Koen J. T.
- New search for: Sun, Yaling
- New search for: Orr, Harry T.
- New search for: Zoghbi, Huda Y.
In:
Human molecular genetics
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12
, 21
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2789-
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2003
- Article (Journal) / Electronic Resource
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Title:Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1
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Contributors:Watase, Kei ( author ) / Venken, Koen J. T. ( author ) / Sun, Yaling ( author ) / Orr, Harry T. ( author ) / Zoghbi, Huda Y. ( author )
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Published in:Human molecular genetics ; 12, 21 ; 2789-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-11-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 12, Issue 21
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 2733
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Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factorsMorabia, Alfredo / Cayanis, Eftihia / Costanza, Michael C. / Ross, Barbara M. / Flaherty, Maria Sol / Alvin, Gabriela B. / Das, Kamna / Gilliam, T. Conrad et al. | 2003
- 2745
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Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart StudyWilk, Jemma B. / DeStefano, Anita L. / Joost, Oscar / Myers, Richard H. / Cupples, L. Adrienne / Slater, Karen / Atwood, Larry D. / Heard-Costa, Nancy L. / Herbert, Alan / O'Connor, George T. et al. | 2003
- 2753
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Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common featureWang, Jiou / Slunt, Hilda / Gonzales, Victoria / Fromholt, David / Coonfield, Michael / Copeland, Neal G. / Jenkins, Nancy A. / Borchelt, David R. et al. | 2003
- 2765
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Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulinSaunders, Aleister J. / Bertram, Lars / Mullin, Kristina / Sampson, Andrew J. / Latifzai, Khushal / Basu, Sanjay / Jones, Jennifer / Kinney, Devon / MacKenzie-Ingano, Laura / Yu, Stephen et al. | 2003
- 2777
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Transgenic overexpression of caveolin-3 in the heart induces a cardiomyopathic phenotypeAravamudan, Bharathi / Volonte, Daniela / Ramani, Ravi / Gursoy, Erdal / Lisanti, Michael P. / London, Barry / Galbiati, Ferruccio et al. | 2003
- 2789
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Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1Watase, Kei / Venken, Koen J. T. / Sun, Yaling / Orr, Harry T. / Zoghbi, Huda Y. et al. | 2003
- 2797
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Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereociliaKarolyi, I. Jill / Probst, Frank J. / Beyer, Lisa / Odeh, Hana / Dootz, Gary / Cha, Kelly B. / Martin, Donna M. / Avraham, Karen B. / Kohrman, David / Dolan, David F. et al. | 2003
- 2807
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The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexesMacedo, Maria G. / Anar, Burcu / Bronner, Iraad F. / Cannella, Milena / Squitieri, Ferdinando / Bonifati, Vincenzo / Hoogeveen, André / Heutink, Peter / Rizzu, Patrizia et al. | 2003
- 2817
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A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)Nimmakayalu, Manjunath A. / Gotter, Anthony L. / Shaikh, Tamim H. / Emanuel, Beverly S. et al. | 2003
- 2827
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Early and reversible neuropathology induced by tetracycline-regulated lentiviral overexpression of mutant huntingtin in rat striatumRégulier, Etienne / Trottier, Yvon / Perrin, Valérie / Aebischer, Patrick / Déglon, Nicole et al. | 2003
- 2837
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Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseasesSiitonen, H. Annika / Kopra, Outi / Kääriäinen, Helena / Haravuori, Henna / Winter, Robin M. / Säämänen, Anna-Marja / Peltonen, Leena / Kestilä, Marjo et al. | 2003
- 2845
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Elucidation of ataxin-3 and ataxin-7 function by integrative bioinformaticsScheel, Hartmut / Tomiuk, Stefan / Hofmann, Kay et al. | 2003
- 2853
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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of {alpha}-dystroglycanLongman, Cheryl / Brockington, Martin / Torelli, Silvia / Jimenez-Mallebrera, Cecilia / Kennedy, Colin / Khalil, Nofal / Feng, Lucy / Saran, Ravindra K. / Voit, Thomas / Merlini, Luciano et al. | 2003
- 2863
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A central nervous system specific mouse model for thanatophoric dysplasia type IILin, Ti / Sandusky, Stacey B. / Xue, Haipeng / Fishbein, Kenneth W. / Spencer, Richard G. / Rao, Mahendra S. / Francomano, Clair A. et al. | 2003