The polyglutamine neurodegenerative protein ataxin-3 binds polyubiquitylated proteins and has ubiquitin protease activity (English)
- New search for: Burnett, Barrington
- New search for: Li, Fusheng
- New search for: Pittman, Randall N.
- New search for: Burnett, Barrington
- New search for: Li, Fusheng
- New search for: Pittman, Randall N.
In:
Human molecular genetics
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12
, 23
;
3195-
;
2003
- Article (Journal) / Electronic Resource
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Title:The polyglutamine neurodegenerative protein ataxin-3 binds polyubiquitylated proteins and has ubiquitin protease activity
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Contributors:
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Published in:Human molecular genetics ; 12, 23 ; 3195-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-12-01
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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 23
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.
- 3043
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A mutation in the canine BHD gene is associated with hereditary multifocal renal cystadenocarcinoma and nodular dermatofibrosis in the German Shepherd dogLingaas, Frode / Comstock, Kenine E. / Kirkness, Ewen F. / Sørensen, Anita / Aarskaug, Tone / Hitte, Christophe / Nickerson, Michael L. / Moe, Lars / Schmidt, Laura S. / Thomas, Rachael et al. | 2003
- 3055
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A frameshifting mutation in CHRNE unmasks skipping of the preceding exonOhno, Kinji / Milone, Margherita / Shen, Xin-Ming / Engel, Andrew G. et al. | 2003
- 3067
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The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporterChen, Li-Sheng / Tassone, Flora / Sahota, Parminder / Hagerman, Paul J. et al. | 2003
- 3075
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Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c geneJohnson, Kenneth R. / Gagnon, Leona H. / Webb, Lisa S. / Peters, Luanne L. / Hawes, Norman L. / Chang, Bo / Zheng, Qing Yin et al. | 2003
- 3087
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Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPsMazroui, Rachid / Huot, Marc-Etienne / Tremblay, Sandra / Boilard, Nathalie / Labelle, Yves / Khandjian, Edouard W. et al. | 2003
- 3097
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Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathyLe Corvoisier, Philippe / Park, Hyun-Young / Carlson, Kerri M. / Marchuk, Douglas A. / Rockman, Howard A. et al. | 2003
- 3109
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Analysis of mammalian proteins involved in chromatin modification reveals new metaphase centromeric proteins and distinct chromosomal distribution patternsCraig, Jeffrey M. / Earle, Elizabeth / Canham, Paul / Wong, Lee H. / Anderson, Melissa / Choo, K.H. Andy et al. | 2003
- 3123
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Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNACerrato, Flavia / Dean, Wendy / Davies, Karen / Kagotani, Kazuhiro / Mitsuya, Kohzoh / Okumura, Katsuzumi / Riccio, Andrea / Reik, Wolf et al. | 2003
- 3133
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Fine mapping of the {alpha}-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigreesErtekin-Taner, Nilüfer / Ronald, James / Asahara, Hideaki / Younkin, Linda / Hella, Maria / Jain, Shushant / Gnida, Eugene / Younkin, Samuel / Fadale, Daniel / Ohyagi, Yasumasa et al. | 2003
- 3145
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The usefulness of different density SNP maps for disease association studies of common variantsWang, William Y. S. / Todd, John A. et al. | 2003
- 3151
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Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effectsHennah, William / Varilo, Teppo / Kestilä, Marjo / Paunio, Tiina / Arajärvi, Ritva / Haukka, Jari / Parker, Alex / Martin, Rory / Levitzky, Steve / Partonen, Timo et al. | 2003
- 3161
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Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulationFernández-Sánchez, Maria Elena / Criado-García, Olga / Heath, Karen E. / García-Fojeda, Belén / Medraño-Fernández, Iria / Gomez-Garre, Pilar / Sanz, Pascual / Serratosa, José María / Rodríguez de Córdoba, Santiago et al. | 2003
- 3173
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Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)de Pontual, Loïc / Népote, Virginie / Attié-Bitach, Tania / Al Halabiah, Hassan / Trang, Ha / Elghouzzi, Vincent / Levacher, Béatrice / Benihoud, Karim / Augé, Joëlle / Faure, Christophe et al. | 2003
- 3181
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Plectin 5'-transcript diversity: short alternative sequences determine stability of gene products, initiation of translation and subcellular localization of isoformsRezniczek, Günther A. / Abrahamsberg, Christina / Fuchs, Peter / Spazierer, Daniel / Wiche, Gerhard et al. | 2003
- 3195
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The polyglutamine neurodegenerative protein ataxin-3 binds polyubiquitylated proteins and has ubiquitin protease activityBurnett, Barrington / Li, Fusheng / Pittman, Randall N. et al. | 2003