Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy (English)
- New search for: Davies, J. E.
- New search for: Sarkar, S.
- New search for: Rubinsztein, D. C.
- New search for: Davies, J. E.
- New search for: Sarkar, S.
- New search for: Rubinsztein, D. C.
In:
HUMAN MOLECULAR GENETICS
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15
, 1
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23-31
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2006
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ISSN:
- Article (Journal) / Print
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Title:Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy
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Contributors:
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Published in:HUMAN MOLECULAR GENETICS ; 15, 1 ; 23-31
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Publisher:
- New search for: Oxford University Press
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Publication date:2006-01-01
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Size:9 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.8 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 15, Issue 1
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.
- 1
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IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancerAl-Zahrani, Ali / Sandhu, Manjinder S. / Luben, Robert N. / Thompson, Deborah / Baynes, Caroline / Pooley, Karen A. / Luccarini, Craig / Munday, Hannah / Perkins, Barbara / Smith, Paula et al. | 2006
- 11
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Loss of polycystin-1 or polycystin-2 results in dysregulated apolipoprotein expression in murine tissues via alterations in nuclear hormone receptorsAllen, Erica / Piontek, Klaus B. / Garrett-Mayer, Elizabeth / Garcia-Gonzalez, Miguel / Gorelick, Kerry Lee / Germino, Gregory G. et al. | 2006
- 23
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Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophyDavies, Janet E. / Sarkar, Sovan / Rubinsztein, David C. et al. | 2006
- 33
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Proteasome impairment does not contribute to pathogenesis in R6/2 Huntingtons disease mice: exclusion of proteasome activator REGg as a therapeutic targetBett, J. S. / Goellner, G. M. / Woodman, B. / Pratt, G. / Rechsteiner, M. / Bates, G. P. et al. | 2006
- 33
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Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington's disease mice: exclusion of proteasome activator REG{gamma} as a therapeutic targetBett, John S. / Goellner, Geoffrey M. / Woodman, Ben / Pratt, Gregory / Rechsteiner, Martin / Bates, Gillian P. et al. | 2006
- 45
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Telomere instability in the male germlineBaird, Duncan M. / Britt-Compton, Bethan / Rowson, Jan / Amso, Nazar N. / Gregory, Linda / Kipling, David et al. | 2006
- 53
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Intracerebral adeno-associated virus-mediated gene transfer in rapidly progressive forms of metachromatic leukodystrophySevin, Caroline / Benraiss, Abdellatif / Van Dam, Debby / Bonnin, Delphine / Nagels, Guy / Verot, Lucie / Laurendeau, Ingrid / Vidaud, Michel / Gieselmann, Volkmar / Vanier, Marie et al. | 2006
- 65
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Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodiesSun, Bo Wen / Yang, A. Cong / Feng, Yun / Sun, Yi Juan / Zhu, Yu fei / Zhang, Yi / Jiang, Hua / Li, Chun Liang / Gao, Fu Rong / Zhang, Zhi Hong et al. | 2006
- 77
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Polymorphisms in the PON gene cluster are associated with Alzheimer diseaseErlich, Porat M. / Lunetta, Kathryn L. / Cupples, L. Adrienne / Huyck, Matthew / Green, Robert C. / Baldwin, Clinton T. / Farrer, Lindsay A. / for the MIRAGE Study Group, et al. | 2006
- 87
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Identification and characterization of the methyl arginines in the fragile X mental retardation protein FmrpStetler, April / Winograd, Claudia / Sayegh, Joyce / Cheever, Anne / Patton, Erin / Zhang, Xing / Clarke, Steven / Ceman, Stephanie et al. | 2006
- 97
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Distinct expression profile in fumarate-hydratase-deficient uterine fibroidsVanharanta, Sakari / Pollard, Patrick J. / Lehtonen, Heli J. / Laiho, Päivi / Sjöberg, Jari / Leminen, Arto / Aittomäki, Kristiina / Arola, Johanna / Kruhoffer, Mogens / Ørntoft, Torben F. et al. | 2006
- 105
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Prevention of oculopharyngeal muscular dystrophy-associated aggregation of nuclear poly(A)-binding protein with a single-domain intracellular antibodyVerheesen, Peter / de Kluijver, Anna / van Koningsbruggen, Silvana / de Brij, Marjolein / de Haard, Hans J. / van Ommen, Gert-Jan B. / van der Maarel, Silvère M. / Verrips, C. Theo et al. | 2006
- 113
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Multidimensional genome scans identify the combinations of genetic loci linked to diabetes-related phenotypes in miceTogawa, Katsuhiko / Moritani, Maki / Yaguchi, Hiroshi / Itakura, Mitsuo et al. | 2006
- 129
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Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3Hernández-Deviez, Delia J. / Martin, Sally / Laval, Steven H. / Lo, Harriet P. / Cooper, Sandra T. / North, Kathryn N. / Bushby, Kate / Parton, Robert G. et al. | 2006
- 143
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Natural competence of mammalian mitochondria allows the molecular investigation of mitochondrial gene expressionKoulintchenko, Milana / Temperley, Richard J. / Mason, Penelope A. / Dietrich, André / Lightowlers, Robert N. et al. | 2006
- 155
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Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15Traherne, James A. / Barcellos, Lisa F. / Sawcer, Stephen J. / Compston, Alastair / Ramsay, Patricia P. / Hauser, Stephen L. / Oksenberg, Jorge R. / Trowsdale, John et al. | 2006
- 163
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Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2Hummelshoj, T. / Munthe-Fog, L. / Madsen, H.O. / Fujita, T. / Matsushita, M. / Garred, P. et al. | 2006
- R1
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Genome-wide location analysis: insights on transcriptional regulationHawkins, R. D. / Ren, B. et al. | 2006
- R9
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Influence of human genome polymorphism on gene expressionPastinen, T. / Ge, B. / Hudson, T. J. et al. | 2006
- R17
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Non-coding RNAMattick, J. S. / Makunin, I. V. et al. | 2006
- R31
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From genome to proteome: developing expression clone resources for the human genomeTemple, G. / Lamesch, P. / Milstein, S. / Hill, D. E. / Wagner, L. / Moore, T. / Vidal, M. et al. | 2006
- R45
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Ethical issues in medical-sequencing research: implications of genotype-phenotype studies for individuals and populationsFoster, M. W. / Sharp, R. R. et al. | 2006
- R51
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Evolution at the nucleotide level: the problem of multiple whole-genome alignmentDewey, C. N. / Pachter, L. et al. | 2006
- R57
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Structural variants: changing the landscape of chromosomes and design of disease studiesFeuk, L. / Marshall, C. R. / Wintle, R. F. / Scherer, S. W. et al. | 2006
- R67
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Lessons from studying monogenic disease for common diseasePeltonen, L. / Perola, M. / Naukkarinen, J. / Palotie, A. et al. | 2006
- R75
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Sleeping beauty: a novel cancer gene discovery toolDupuy, A. J. / Jenkins, N. A. / Copeland, N. G. et al. | 2006
- R81
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Integrating biological data through the genomeReeves, G. A. / Thornton, J. M. et al. | 2006
- R89
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Pharmacogenomics: from bedside to clinical practiceMarsh, S. / McLeod, H. L. et al. | 2006
- R95
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The emerging science of epigenomicsCallinan, P. A. / Feinberg, A. P. et al. | 2006