Contents Page (Englisch)
In:
HUMAN MOLECULAR GENETICS
;
23
, 16
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NP-NP
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2014
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ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:Contents Page
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Erschienen in:HUMAN MOLECULAR GENETICS ; 23, 16 ; 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
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Inhaltsverzeichnis – Band 23, Ausgabe 16
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Treatment with an antibody directed against Nogo-A delays disease progression in the SOD1G93A mouse model of Amyotrophic lateral sclerosisBros-Facer, V. / Krull, D. / Taylor, A. / Dick, J. R. / Bates, S. A. / Cleveland, M. S. / Prinjha, R. K. / Greensmith, L. et al. | 2014
- 4201
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Membrane recruitment of endogenous LRRK2 precedes its potent regulation of autophagySchapansky, J. / Nardozzi, J. D. / Felizia, F. / LaVoie, M. J. et al. | 2014
- 4215
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Tbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of masticationKong, P. / Racedo, S. E. / Macchiarulo, S. / Hu, Z. / Carpenter, C. / Guo, T. / Wang, T. / Zheng, D. / Morrow, B. E. et al. | 2014
- 4232
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RAD50 phosphorylation promotes ATR downstream signaling and DNA restart following replication stressGatei, M. / Kijas, A. W. / Biard, D. / Dörk, T. / Lavin, M. F. et al. | 2014
- 4249
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Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophyBoyer, J. G. / Deguise, M. O. / Murray, L. M. / Yazdani, A. / De Repentigny, Y. / Boudreau-Larivière, C. l. / Kothary, R. et al. | 2014
- 4260
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Regulation of a novel isoform of Receptor Expression Enhancing Protein REEP6 in rod photoreceptors by bZIP transcription factor NRLHao, H. / Veleri, S. / Sun, B. / Kim, D. S. / Keeley, P. W. / Kim, J. W. / Yang, H. J. / Yadav, S. P. / Manjunath, S. H. / Sood, R. et al. | 2014
- 4272
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Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformationsRussell, M. W. / Raeker, M. O. / Geisler, S. B. / Thomas, P. E. / Simmons, T. A. / Bernat, J. A. / Thorsson, T. / Innis, J. W. et al. | 2014
- 4285
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Cellular consequences of oxidative stress in riboflavin responsive multiple acyl-CoA dehydrogenation deficiency patient fibroblastsCornelius, N. / Corydon, T. J. / Gregersen, N. / Olsen, R. K. et al. | 2014
- 4302
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Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in XenopusRoberts, N. A. / Woolf, A. S. / Stuart, H. M. / Thuret, R. l. / McKenzie, E. A. / Newman, W. G. / Hilton, E. N. et al. | 2014
- 4315
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Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesisFlex, E. / Jaiswal, M. / Pantaleoni, F. / Martinelli, S. / Strullu, M. / Fansa, E. K. / Caye, A. l. / De Luca, A. / Lepri, F. / Dvorsky, R. et al. | 2014
- 4328
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Inhibition of soluble tumor necrosis factor is therapeutic in Huntington's diseaseHsiao, H. Y. / Chiu, F. L. / Chen, C. M. / Wu, Y. R. / Chen, H. M. / Chen, Y. C. / Kuo, H. C. / Chern, Y. et al. | 2014
- 4345
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Distinct pathways leading to TDP-43-induced cellular dysfunctionsYamashita, M. / Nonaka, T. / Hirai, S. / Miwa, A. / Okado, H. / Arai, T. / Hosokawa, M. / Akiyama, H. / Hasegawa, M. et al. | 2014
- 4357
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Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesisMcDonald, D. A. / Shi, C. / Shenkar, R. / Gallione, C. J. / Akers, A. L. / Li, S. / De Castro, N. / Berg, M. J. / Corcoran, D. L. / Awad, I. A. et al. | 2014
- 4371
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SIK1 localizes with nephrin in glomerular podocytes and its polymorphism predicts kidney injuryFerrandi, M. / Molinari, I. / Matafora, V. / Zerbini, G. / Trevisani, F. / Rastaldi, M. P. / Simonini, M. / Giardino, L. / Ferrari, P. / Manunta, P. et al. | 2014
- 4383
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WIP modulates dendritic spine actin cytoskeleton by transcriptional control of lipid metabolic enzymesFranco-Villanueva, A. / Fernández-López, E. a. / Gabandé-Rodríguez, E. / Bañón-Rodríguez, I. / Esteban, J. A. / Antón, I. s. / Ledesma, M. a. et al. | 2014
- 4396
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CHARGE and Kabuki syndromes: a phenotypic and molecular linkSchulz, Y. / Freese, L. / Mänz, J. / Zoll, B. / Völter, C. / Brockmann, K. / Bögershausen, N. / Becker, J. / Wollnik, B. / Pauli, S. et al. | 2014
- 4406
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NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndromeIzzo, A. / Manco, R. / Bonfiglio, F. / Calì, G. / De Cristofaro, T. / Patergnani, S. / Cicatiello, R. / Scrima, R. / Zannini, M. / Pinton, P. et al. | 2014
- 4420
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Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of ageDeelen, J. / Beekman, M. / Uh, H. W. / Broer, L. / Ayers, K. L. / Tan, Q. / Kamatani, Y. / Bennet, A. M. / Tamm, R. / Trompet, S. et al. | 2014
- 4433
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A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in KoreansKwak, S. H. / Park, Y. J. / Go, M. J. / Lee, K. E. / Kim, S. j. / Choi, H. S. / Kim, T. H. / Choi, S. H. / Lim, S. / Kim, K. W. et al. | 2014
- 4443
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Predicting HLA alleles from high-resolution SNP data in three Southeast Asian populationsPillai, N. E. / Okada, Y. / Saw, W. Y. / Ong, R. T. / Wang, X. / Tantoso, E. / Xu, W. / Peterson, T. A. / Bielawny, T. / Ali, M. et al. | 2014
- 4452
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Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male pubertyCousminer, D. L. / Stergiakouli, E. / Berry, D. J. / Ang, W. / Groen-Blokhuis, M. M. / Körner, A. / Siitonen, N. / Ntalla, I. / Marinelli, M. / Perry, J. R. et al. | 2014
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