Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in Drosophila (English)
- New search for: Humphrey, D. M.
- New search for: Parsons, R. B.
- New search for: Ludlow, Z. N.
- New search for: Riemensperger, T.
- New search for: Esposito, G.
- New search for: Verstreken, P.
- New search for: Jacobs, H. T.
- New search for: Birman, S.
- New search for: Hirth, F.
- New search for: Humphrey, D. M.
- New search for: Parsons, R. B.
- New search for: Ludlow, Z. N.
- New search for: Riemensperger, T.
- New search for: Esposito, G.
- New search for: Verstreken, P.
- New search for: Jacobs, H. T.
- New search for: Birman, S.
- New search for: Hirth, F.
In:
HUMAN MOLECULAR GENETICS
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21
, 12
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2698-2712
;
2012
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ISSN:
- Article (Journal) / Print
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Title:Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in Drosophila
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Contributors:Humphrey, D. M. ( author ) / Parsons, R. B. ( author ) / Ludlow, Z. N. ( author ) / Riemensperger, T. ( author ) / Esposito, G. ( author ) / Verstreken, P. ( author ) / Jacobs, H. T. ( author ) / Birman, S. ( author ) / Hirth, F. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 21, 12 ; 2698-2712
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Publisher:
- New search for: Oxford University Press
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Publication date:2012-01-01
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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 21, Issue 12
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.
- 2619
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Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cellsZuercher, J. / Fritzsche, M. / Feil, S. / Mohn, L. / Berger, W. et al. | 2012
- 2631
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Human and mouse ZFY genes produce a conserved testis-specific transcript encoding a zinc finger protein with a short acidic domain and modified transactivation potentialDecarpentrie, F. / Vernet, N. x. / Mahadevaiah, S. K. / Longepied, G. / Streichemberger, E. / Aknin-Seifer, I. / Ojarikre, O. A. / Burgoyne, P. S. / Metzler-Guillemain, C. / Mitchell, M. J. et al. | 2012
- 2646
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Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosisBras, J. / Verloes, A. / Schneider, S. A. / Mole, S. E. / Guerreiro, R. J. et al. | 2012
- 2651
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Disruption and therapeutic rescue of autophagy in a human neuronal model of Niemann Pick type C1Ordonez, M. P. / Roberts, E. A. / Kidwell, C. U. / Yuan, S. H. / Plaisted, W. C. / Goldstein, L. S. et al. | 2012
- 2663
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Genetic ablation of Pals1 in retinal progenitor cells models the retinal pathology of Leber congenital amaurosisCho, S. H. / Kim, J. Y. / Simons, D. L. / Song, J. Y. / Le, J. H. / Swindell, E. C. / Jamrich, M. / Wu, S. M. / Kim, S. et al. | 2012
- 2677
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Imprinting control region (ICR) of the Peg3 domainKim, J. / Ekram, M. B. / Kim, H. / Faisal, M. / Frey, W. D. / Huang, J. M. / Tran, K. / Kim, M. M. / Yu, S. et al. | 2012
- 2688
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Friedreich's ataxia reveals a mechanism for coordinate regulation of oxidative metabolism via feedback inhibition of the SIRT3 deacetylaseWagner, G. R. / Pride, P. M. / Babbey, C. M. / Payne, R. M. et al. | 2012
- 2698
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Alternative oxidase rescues mitochondria-mediated dopaminergic cell loss in DrosophilaHumphrey, D. M. / Parsons, R. B. / Ludlow, Z. N. / Riemensperger, T. / Esposito, G. / Verstreken, P. / Jacobs, H. T. / Birman, S. / Hirth, F. et al. | 2012
- 2713
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Impaired neurotransmission in ether lipid-deficient nerve terminalsBrodde, A. / Teigler, A. / Brugger, B. / Lehmann, W. D. / Wieland, F. / Berger, J. / Just, W. W. et al. | 2012
- 2725
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Neuropathogenic role of adenylate kinase-1 in Aβ-mediated tau phosphorylation via AMPK and GSK3βPark, H. / Kam, T. I. / Kim, Y. / Choi, H. / Gwon, Y. / Kim, C. / Koh, J. Y. / Jung, Y. K. et al. | 2012
- 2738
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Response to DNA damage of CHEK2 missense mutations in familial breast cancerRoeb, W. / Higgins, J. / King, M. C. et al. | 2012
- 2745
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The zinc finger protein ZPR1 is a potential modifier of spinal muscular atrophyAhmad, S. / Wang, Y. / Shaik, G. M. / Burghes, A. H. / Gangwani, L. et al. | 2012
- 2759
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Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in humanRoux-Buisson, N. / Cacheux, M. / Fourest-Lieuvin, A. / Fauconnier, J. / Brocard, J. / Denjoy, I. / Durand, P. / Guicheney, P. / Kyndt, F. / Leenhardt, A. et al. | 2012
- 2768
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Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sitesHannan, F. M. / Nesbit, M. A. / Zhang, C. / Cranston, T. / Curley, A. J. / Harding, B. / Fratter, C. / Rust, N. / Christie, P. T. / Turner, J. J. et al. | 2012
- 2779
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DISC1 variants 37W and 607F disrupt its nuclear targeting and regulatory role in ATF4-mediated transcriptionMalavasi, E. L. / Ogawa, F. / Porteous, D. J. / Millar, J. K. et al. | 2012
- 2793
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Respiratory syncytial virus potentiates ABCA3 mutation-induced loss of lung epithelial cell differentiationKaltenborn, E. / Kern, S. x. / Frixel, S. / Fragnet, L. / Conzelmann, K. K. / Zarbock, R. / Griese, M. et al. | 2012
- 2807
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Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6Strokin, M. / Seburn, K. L. / Cox, G. A. / Martens, K. A. / Reiser, G. et al. | 2012
- 2815
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Statistical colocalization of monocyte gene expression and genetic risk variants for type 1 diabetesWallace, C. / Rotival, M. / Cooper, J. D. / Rice, C. M. / Yang, J. H. / McNeill, M. / Smyth, D. J. / Niblett, D. / Cambien, F. x. / Tiret, L. et al. | 2012
- 2825
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Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-upMartin, J. E. / Broen, J. C. / Carmona, F. D. / Teruel, M. / Simeon, C. P. / Vonk, M. C. / van ‘ / t Slot, R. / Rodriguez-Rodriguez, L. / Vicente, E. et al. | 2012
- 2836
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A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucomaOsman, W. / Low, S. K. / Takahashi, A. / Kubo, M. / Nakamura, Y. et al. | 2012
- 2843
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Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patientsHumphreys, R. / Zheng, W. / Prince, L. S. / Qu, X. / Brown, C. / Loomes, K. / Huppert, S. S. / Baldwin, S. / Goudy, S. et al. | 2012
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