Integrating with integrity (Englisch)
In:
NATURE GENETICS
;
42
, 1
;
1-1
;
2010
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ISSN:
- Aufsatz (Zeitschrift) / Print
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Titel:Integrating with integrity
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Erschienen in:NATURE GENETICS ; 42, 1 ; 1-1
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Verlag:
- Neue Suche nach: Nature Publishing Group
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Erscheinungsdatum:01.01.2010
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Format / Umfang:1 pages
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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: 576.5
- Weitere Informationen zu Dewey Decimal Classification
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Klassifikation:
DDC: 576.5 -
Datenquelle:
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Integrating with integrity| 2010
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No evidence for a role of CLCN2 variants in idiopathic generalized epilepsyNiemeyer, M. I. / Cid, L. P. / Sepulveda, F. V. / Blanz, J. / Auberson, M. / Jentsch, T. J. et al. | 2010
- 4
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Reassessing the abundance of H3K9me2 chromatin domains in embryonic stem cellsFilion, G. J. / van Steensel, B. et al. | 2010
- 5
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Reply to “Reassessing the abundance of H3K9me2 chromatin domains in embryonic stem cells”Wen, B. / Wu, H. / Shinkai, Y. / Irizarry, R. A. / Feinberg, A. P. et al. | 2010
- 6
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Evolutionary flux of canonical microRNAs and mirtrons in DrosophilaBerezikov, E. / Liu, N. / Flynt, A. S. / Hodges, E. / Rooks, M. / Hannon, G. J. / Lai, E. C. et al. | 2010
- 9
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Reply to “Evolutionary flux of canonical microRNAs and mirtrons in Drosophila”Lu, J. / Shen, Y. / Carthew, R. W. / Wang, S. M. / Wu, C. I. et al. | 2010
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Exome sequencing makes medical genomics a realityBiesecker, L. G. et al. | 2010
- 14
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Lung function and airway diseasesWeiss, S. T. et al. | 2010
- 16
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Getting connected in the globin interactomeRagoczy, T. / Groudine, M. et al. | 2010
- 19
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Research highlightsBahcall, O. / Colosimo, P. / Niemitz, E. / Vogan, K. et al. | 2010
- 21
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Variant in PNPLA3 is associated with alcoholic liver diseaseTian, C. / Stokowski, R. P. / Kershenobich, D. / Ballinger, D. G. / Hinds, D. A. et al. | 2010
- 24
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Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palateMangold, E. / Ludwig, K. U. / Birnbaum, S. / Baluardo, C. / Ferrian, M. / Herms, S. / Reutter, H. / de Assis, N. A. / Chawa, T. A. / Mattheisen, M. et al. | 2010
- 27
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A restricted spectrum of NRAS mutations causes Noonan syndromeCirstea, I. C. / Kutsche, K. / Dvorsky, R. / Gremer, L. / Carta, C. / Horn, D. / Roberts, A. E. / Lepri, F. / Merbitz-Zahradnik, T. / Konig, R. et al. | 2010
- 30
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Exome sequencing identifies the cause of a mendelian disorderNg, S. B. / Buckingham, K. J. / Lee, C. / Bigham, A. W. / Tabor, H. K. / Dent, K. M. / Huff, C. D. / Shannon, P. T. / Jabs, E. W. / Nickerson, D. A. et al. | 2010
- 36
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Genome-wide association study identifies five loci associated with lung functionRepapi, E. / Sayers, I. / Wain, L. V. / Burton, P. R. / Johnson, T. / Obeidat, M. e. / Zhao, J. H. / Ramasamy, A. / Zhai, G. / Vitart, V. et al. | 2010
- 45
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Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary functionHancock, D. B. / Eijgelsheim, M. / Wilk, J. B. / Gharib, S. A. / Loehr, L. R. / Marciante, K. D. / Franceschini, N. / van Durme, Y. M. / Chen, T. h. / Barr, R. G. et al. | 2010
- 53
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Preferential associations between co-regulated genes reveal a transcriptional interactome in erythroid cellsSchoenfelder, S. / Sexton, T. / Chakalova, L. / Cope, N. F. / Horton, A. / Andrews, S. / Kurukuti, S. / Mitchell, J. A. / Umlauf, D. / Dimitrova, D. S. et al. | 2010
- 62
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Geographical genomics of human leukocyte gene expression variation in southern MoroccoIdaghdour, Y. / Czika, W. / Shianna, K. V. / Lee, S. H. / Visscher, P. M. / Martin, H. C. / Miclaus, K. / Jadallah, S. J. / Goldstein, D. B. / Wolfinger, R. D. et al. | 2010
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The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetesWallace, C. / Smyth, D. J. / Maisuria-Armer, M. / Walker, N. M. / Todd, J. A. / Clayton, D. G. et al. | 2010
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Mutations in the formin gene INF2 cause focal segmental glomerulosclerosisBrown, E. J. / Schlondorff, J. S. / Becker, D. J. / Tsukaguchi, H. / Uscinski, A. L. / Higgs, H. N. / Henderson, J. M. / Pollak, M. R. et al. | 2010
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Somatic mutations of the Parkinson's disease–associated gene PARK2 in glioblastoma and other human malignanciesVeeriah, S. / Taylor, B. S. / Meng, S. / Fang, F. / Yilmaz, E. / Vivanco, I. / Janakiraman, M. / Schultz, N. / Hanrahan, A. J. / Pao, W. et al. | 2010
- 83
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Skp2 is required for survival of aberrantly proliferating Rb1-deficient cells and for tumorigenesis in Rb1+/− miceWang, H. / Bauzon, F. / Ji, P. / Xu, X. / Sun, D. / Locker, J. / Sellers, R. S. / Nakayama, K. / Nakayama, K. I. / Cobrinik, D. et al. | 2010
- 89
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Wt1 is required for cardiovascular progenitor cell formation through transcriptional control of Snail and E-cadherinMartinez-Estrada, O. M. / Lettice, L. A. / Essafi, A. / Guadix, J. A. / Slight, J. / Velecela, V. / Hall, E. / Reichmann, J. / Devenney, P. S. / Hohenstein, P. et al. | 2010