Inhibiting sphingosine kinase 2 mitigates mutant Huntingtin-induced neurodegeneration in neuron models of Huntington disease (English)
- New search for: Moruno-Manchon, J. F.
- New search for: Uzor, N. E.
- New search for: Blasco-Conesa, M. P.
- New search for: Mannuru, S.
- New search for: Putluri, N.
- New search for: Furr-Stimming, E. E.
- New search for: Tsvetkov, A. S.
- New search for: Moruno-Manchon, J. F.
- New search for: Uzor, N. E.
- New search for: Blasco-Conesa, M. P.
- New search for: Mannuru, S.
- New search for: Putluri, N.
- New search for: Furr-Stimming, E. E.
- New search for: Tsvetkov, A. S.
In:
HUMAN MOLECULAR GENETICS
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26
, 7
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1305-1317
;
2017
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ISSN:
- Article (Journal) / Print
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Title:Inhibiting sphingosine kinase 2 mitigates mutant Huntingtin-induced neurodegeneration in neuron models of Huntington disease
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Contributors:Moruno-Manchon, J. F. ( author ) / Uzor, N. E. ( author ) / Blasco-Conesa, M. P. ( author ) / Mannuru, S. ( author ) / Putluri, N. ( author ) / Furr-Stimming, E. E. ( author ) / Tsvetkov, A. S. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 26, 7 ; 1305-1317
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Publisher:
- New search for: Oxford University Press
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Publication date:2017-01-01
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Size:13 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 26, Issue 7
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.
- 1219
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Klinefelter syndrome comorbidities linked to increased X chromosome gene dosage and altered protein interactome activityBelling, K. / Russo, F. / Jensen, A. B. / Dalgaard, M. D. / Westergaard, D. / Rajpert-De Meyts, E. / Skakkebæk, N. E. / Juul, A. / Brunak, S. r. et al. | 2017
- 1230
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Therapeutic potential of AAV-mediated MMP-3 secretion from corneal endothelium in treating glaucomaO’Callaghan, J. / Crosbie, D. E. / Cassidy, P. S. / Sherwood, J. M. / Flügel-Koch, C. / Lütjen-Drecoll, E. / Humphries, M. M. / Reina-Torres, E. / Wallace, D. / Kiang, A. S. et al. | 2017
- 1247
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LRRK2(I2020T) functional genetic interactors that modify eye degeneration and dopaminergic cell loss in DrosophilaMarcogliese, P. C. / Abuaish, S. / Kabbach, G. / Abdel-Messih, E. / Seang, S. / Li, G. / Slack, R. S. / Haque, M. E. / Venderova, K. / Park, D. S. et al. | 2017
- 1258
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Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levelsShin, A. / Shin, B. / Shin, J. W. / Kim, K. H. / Atwal, R. S. / Hope, J. M. / Gillis, T. / Leszyk, J. D. / Shaffer, S. A. / Lee, R. et al. | 2017
- 1268
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Rdh10 loss-of-function and perturbed retinoid signaling underlies the etiology of choanal atresiaKurosaka, H. / Wang, Q. / Sandell, L. / Yamashiro, T. / Trainor, P. A. et al. | 2017
- 1280
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A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndromeTang, L. / Wu, X. / Zhang, H. / Lu, S. / Wu, M. / Shen, C. / Chen, X. / Wang, Y. / Wang, W. / Shen, Y. et al. | 2017
- 1294
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Opposing FlnA and FlnB interactions regulate RhoA activation in guiding dynamic actin stress fiber formation and cell spreadingHu, J. / Lu, J. / Goyal, A. / Wong, T. / Lian, G. / Zhang, J. / Hecht, J. L. / Feng, Y. / Sheen, V. L. et al. | 2017
- 1305
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Inhibiting sphingosine kinase 2 mitigates mutant Huntingtin-induced neurodegeneration in neuron models of Huntington diseaseMoruno-Manchon, J. F. / Uzor, N. E. / Blasco-Conesa, M. P. / Mannuru, S. / Putluri, N. / Furr-Stimming, E. E. / Tsvetkov, A. S. et al. | 2017
- 1318
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Sex specific activation of the ERα axis of the mitochondrial UPR (UPRmt) in the G93A-SOD1 mouse model of familial ALSRiar, A. K. / Burstein, S. R. / Palomo, G. M. / Arreguin, A. / Manfredi, G. / Germain, D. et al. | 2017
- 1328
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Mitochondrial complex II regulates a distinct oxygen sensing mechanism in monocytesSharma, S. / Wang, J. / Cortes Gomez, E. / Taggart, R. T. / Baysal, B. E. et al. | 2017
- 1340
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Fragile X related protein 1 (FXR1P) regulates proliferation of adult neural stem cellsPatzlaff, N. E. / Nemec, K. M. / Malone, S. G. / Li, Y. / Zhao, X. et al. | 2017
- 1353
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AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse modelVerhelle, A. / Nair, N. / Everaert, I. / Van Overbeke, W. / Supply, L. / Zwaenepoel, O. / Peleman, C. / Van Dorpe, J. / Lahoutte, T. / Devoogdt, N. et al. | 2017
- 1365
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Cowden syndrome-associated germline succinate dehydrogenase complex subunit D (SDHD) variants cause PTEN-mediated down-regulation of autophagy in thyroid cancer cellsYu, W. / Ni, Y. / Saji, M. / Ringel, M. D. / Jaini, R. / Eng, C. et al. | 2017
- 1376
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Gclc deficiency in mouse CNS causes mitochondrial damage and neurodegenerationFeng, W. / Rosca, M. / Fan, Y. / Hu, Y. / Feng, P. / Lee, H. G. / Monnier, V. M. / Fan, X. et al. | 2017
- 1391
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GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition lociJones, A. V. / Tilley, M. / Gutteridge, A. / Hyde, C. / Nagle, M. / Ziemek, D. / Gorman, D. / Fauman, E. B. / Chen, X. / Miller, M. R. et al. | 2017