Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases (English)
- New search for: Branco, J.
- New search for: Al-Ramahi, I.
- New search for: Ukani, L.
- New search for: Perez, A. M.
- New search for: Fernandez-Funez, P.
- New search for: Rincon-Limas, D.
- New search for: Botas, J.
- New search for: Branco, J.
- New search for: Al-Ramahi, I.
- New search for: Ukani, L.
- New search for: Perez, A. M.
- New search for: Fernandez-Funez, P.
- New search for: Rincon-Limas, D.
- New search for: Botas, J.
In:
HUMAN MOLECULAR GENETICS
;
17
, 3
;
376-390
;
2008
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ISSN:
- Article (Journal) / Print
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Title:Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases
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Contributors:Branco, J. ( author ) / Al-Ramahi, I. ( author ) / Ukani, L. ( author ) / Perez, A. M. ( author ) / Fernandez-Funez, P. ( author ) / Rincon-Limas, D. ( author ) / Botas, J. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 17, 3 ; 376-390
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Publisher:
- New search for: Oxford University Press
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Publication date:2008-01-01
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Size:15 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 17, Issue 3
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.
- 331
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Genetic determinants of emotionality and stress response in AcB/BcA recombinant congenic mice and in silico evidence of convergence with cardiovascular candidate genesThifault, Stéphane / Ondrej, Seda / Sun, Yulin / Fortin, Anny / Skamene, Emil / Lalonde, Robert / Tremblay, Johanne / Hamet, Pavel et al. | 2008
- 345
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Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxicTakahashi, Toshiaki / Kikuchi, Shinya / Katada, Shinichi / Nagai, Yoshitaka / Nishizawa, Masatoyo / Onodera, Osamu et al. | 2008
- 357
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Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgeryLabarque, Veerle / Freson, Kathleen / Thys, Chantal / Wittevrongel, Christine / Hoylaerts, Marc F. / De Vos, Rita / Goemans, Nathalie / Van Geet, Chris et al. | 2008
- 367
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Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of Charcot-Marie-Tooth type 2ADetmer, Scott A. / Velde, Christine Vande / Cleveland, Don W. / Chan, David C. et al. | 2008
- 376
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Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseasesBranco, Joana / Al-Ramahi, Ismael / Ukani, Lubna / Pérez, Alma M. / Fernandez-Funez, Pedro / Rincón-Limas, Diego / Botas, Juan et al. | 2008
- 391
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In vivo YY1 knockdown effects on genomic imprintingKim, Joomyeong / Kim, Jeong Do et al. | 2008
- 402
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Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activityNornes, Svanhild / Newman, Morgan / Verdile, Giuseppe / Wells, Simon / Stoick-Cooper, Cristi L. / Tucker, Ben / Frederich-Sleptsova, Inna / Martins, Ralph / Lardelli, Michael et al. | 2008
- 413
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Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressureFava, C. / Montagnana, M. / Rosberg, L. / Burri, P. / Almgren, P. / Jönsson, A. / Wanby, P. / Lippi, G. / Minuz, P. / Hulthèn, L.U. et al. | 2008
- 419
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Germline mutations of MEK in cardio-facio-cutaneous syndrome are sensitive to MEK and RAF inhibition: implications for therapeutic optionsSenawong, Thanaset / Phuchareon, Janyaporn / Ohara, Osamu / McCormick, Frank / Rauen, Katherine A. / Tetsu, Osamu et al. | 2008
- 431
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Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseasesTan, Jeanne M.M. / Wong, Esther S.P. / Kirkpatrick, Donald S. / Pletnikova, Olga / Ko, Han Seok / Tay, Shiam-Peng / Ho, Michelle W.L. / Troncoso, Juan / Gygi, Steven P. / Lee, Michael K. et al. | 2008
- 440
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Genomic and functional profiling of human Down syndrome neural progenitors implicates S100B and aquaporin 4 in cell injuryEsposito, Giuseppe / Imitola, Jaime / Lu, Jie / De Filippis, Daniele / Scuderi, Caterina / Ganesh, Vijay S. / Folkerth, Rebecca / Hecht, Jonathan / Shin, Soojung / Iuvone, Teresa et al. | 2008
- 458
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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophreniaKirov, George / Gumus, Dilihan / Chen, Wei / Norton, Nadine / Georgieva, Lyudmila / Sari, Murat / ODonovan, Michael C / Erdogan, Fikret / Owen, Michael J / Ropers, Hans-Hilger et al. | 2008
- 466
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Copy-number variation in control population cohortsPinto, Dalila / Marshall, Christian / Feuk, Lars / Scherer, Stephen W. et al. | 2008
- 468
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Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cellsKandert, Sebastian / Lüke, Yvonne / Kleinhenz, Tobias / Neumann, Sascha / Lu, Wenshu / Jaeger, Verena M. / Munck, Martina / Wehnert, Manfred / Müller, Clemens R. / Zhou, Zhongjun et al. | 2008