Editorial Board (Englisch)
In:
HUMAN MOLECULAR GENETICS
;
23
, 18
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NP-NP
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2014
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ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:Editorial Board
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Erschienen in:HUMAN MOLECULAR GENETICS ; 23, 18 ; NP-NP
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Verlag:
- Neue Suche nach: Oxford University Press
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Erscheinungsdatum:01.01.2014
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Format / Umfang:NP-NP
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ISSN:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Print
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Sprache:Englisch
- Neue Suche nach: 572.8
- Weitere Informationen zu Dewey Decimal Classification
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Klassifikation:
DDC: 572.8 -
Datenquelle:
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Inhaltsverzeichnis – Band 23, Ausgabe 18
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- 4745
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Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamicsBricceno, K. V. / Martinez, T. / Leikina, E. / Duguez, S. / Partridge, T. A. / Chernomordik, L. V. / Fischbeck, K. H. / Sumner, C. J. / Burnett, B. G. et al. | 2014
- 4758
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Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2Fogel, B. L. / Cho, E. / Wahnich, A. / Gao, F. / Becherel, O. J. / Wang, X. / Fike, F. / Chen, L. / Criscuolo, C. / De Michele, G. et al. | 2014
- 4770
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Cisd2 modulates the differentiation and functioning of adipocytes by regulating intracellular Ca2+ homeostasisWang, C. H. / Chen, Y. F. / Wu, C. Y. / Wu, P. C. / Huang, Y. L. / Kao, C. H. / Lin, C. H. / Kao, L. S. / Tsai, T. F. / Wei, Y. H. et al. | 2014
- 4786
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Rapid depletion of muscle progenitor cells in dystrophic mdx/utrophin−/− miceLu, A. / Poddar, M. / Tang, Y. / Proto, J. D. / Sohn, J. / Mu, X. / Oyster, N. / Wang, B. / Huard, J. et al. | 2014
- 4801
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A unique gene expression signature associated with serotonin 2C receptor RNA editing in the prefrontal cortex and altered in suicideDi Narzo, A. F. / Kozlenkov, A. / Roussos, P. / Hao, K. / Hurd, Y. / Lewis, D. A. / Sibille, E. / Siever, L. J. / Koonin, E. / Dracheva, S. et al. | 2014
- 4814
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The genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's diseaseLinnertz, C. / Lutz, M. W. / Ervin, J. F. / Allen, J. / Miller, N. R. / Welsh-Bohmer, K. A. / Roses, A. D. / Chiba-Falek, O. et al. | 2014
- 4822
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Connective tissue alterations in Fkbp10−/− miceLietman, C. D. / Rajagopal, A. / Homan, E. P. / Munivez, E. / Jiang, M. M. / Bertin, T. K. / Chen, Y. / Hicks, J. / Weis, M. / Eyre, D. et al. | 2014
- 4832
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Morpholino antisense oligonucleotides targeting intronic repressor Element1 improve phenotype in SMA mouse modelsOsman, E. Y. / Miller, M. R. / Robbins, K. L. / Lombardi, A. M. / Atkinson, A. K. / Brehm, A. J. / Lorson, C. L. et al. | 2014
- 4846
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The genetic landscape of infantile spasmsMichaud, J. L. / Lachance, M. / Hamdan, F. F. / Carmant, L. / Lortie, A. / Diadori, P. / Major, P. / Meijer, I. A. / Lemyre, E. / Cossette, P. et al. | 2014
- 4859
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Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegiaPérez-BrangulÃ, F. / Mishra, H. K. / Prots, I. / Havlicek, S. / Kohl, Z. / Saul, D. / Rummel, C. / Dorca-Arevalo, J. / Regensburger, M. / Graef, D. et al. | 2014
- 4875
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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotypeAmbrosini, E. / Sicca, F. / Brignone, M. S. / D'Adamo, M. C. / Napolitano, C. / Servettini, I. / Moro, F. / Ruan, Y. / Guglielmi, L. / Pieroni, S. et al. | 2014
- 4887
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A Parkinson's disease gene regulatory network identifies the signaling protein RGS2 as a modulator of LRRK2 activity and neuronal toxicityDusonchet, J. / Li, H. / Guillily, M. / Liu, M. / Stafa, K. / Derada Troletti, C. / Boon, J. Y. / Saha, S. / Glauser, L. / Mamais, A. et al. | 2014
- 4906
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Genetic deletion of TNFRII gene enhances the Alzheimer-like pathology in an APP transgenic mouse model via reduction of phosphorylated IκBαJiang, H. / He, P. / Xie, J. / Staufenbiel, M. / Li, R. / Shen, Y. et al. | 2014
- 4919
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An mTOR anti-sense oligonucleotide decreases polycystic kidney disease in mice with a targeted mutation in Pkd2Ravichandran, K. / Zafar, I. / He, Z. / Doctor, R. B. / Moldovan, R. / Mullick, A. E. / Edelstein, C. L. et al. | 2014
- 4932
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Calpain inhibition reduces ataxin-3 cleavage alleviating neuropathology and motor impairments in mouse models of Machado–Joseph diseaseSimões, A. T. / Gonçalves, N. l. / Nobre, R. J. / Duarte, C. B. / Pereira de Almeida, L. s. et al. | 2014
- 4945
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Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegansJuang, B. T. / Ludwig, A. L. / Benedetti, K. L. / Gu, C. / Collins, K. / Morales, C. / Asundi, A. / Wittmann, T. / L'Etoile, N. / Hagerman, P. J. et al. | 2014
- 4960
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Parkin-mediated reduction of nuclear and soluble TDP-43 reverses behavioral decline in symptomatic miceWenqiang, C. / Lonskaya, I. / Hebron, M. L. / Ibrahim, Z. / Olszewski, R. T. / Neale, J. H. / Moussa, C. E. et al. | 2014
- 4970
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Comparison of epigenetic mediator expression and function in mouse and human embryonic blastomeresChavez, S. L. / McElroy, S. L. / Bossert, N. L. / De Jonge, C. J. / Rodriguez, M. V. / Leong, D. E. / Behr, B. / Westphal, L. M. / Reijo Pera, R. A. et al. | 2014
- 4985
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X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansionAdihe Lokanga, R. / Zhao, X. N. / Entezam, A. / Usdin, K. et al. | 2014
- 4995
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Genetically altering organismal metabolism by leptin-deficiency benefits a mouse model of amyotrophic lateral sclerosisLim, M. A. / Bence, K. K. / Sandesara, I. / Andreux, P. n. / Auwerx, J. / Ishibashi, J. / Seale, P. / Kalb, R. G. et al. | 2014
- 5009
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Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemiaHouten, S. M. / Denis, S. / te Brinke, H. / Jongejan, A. / van Kampen, A. H. / Bradley, E. J. / Baas, F. / Hennekam, R. C. / Millington, D. S. / Young, S. P. et al. | 2014
- 5017
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Pharmacogenomics: novel loci identification via integrating gene differential analysis and eQTL analysisQiu, W. / Rogers, A. J. / Damask, A. / Raby, B. A. / Klanderman, B. J. / Duan, Q. L. / Tyagi, S. / Niu, S. / Anderson, C. / Cahir-Mcfarland, E. et al. | 2014
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