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mutation genome browser phenotype ucsc genome browser database variant information locus genome browser track locus variants track encode region sequence project table disease phencode blood example university encode project consortium color ¢ gure result deletion script institute data sources details page source query pennsylvania state university function 2002. patient apoa 5 gene 10.1002/ reference swiss-prot detail variation consortium grant issue genomic grant sponsor group recombination field hbvar cluster beta-globin entry coordinate element lsdb curators encode project fibrosis protein pahdb chromosome coordinates sponsor display ucsc tables genome research institute genome browser view system genphen k 562 cells nomenclature cfmdb medicine 2005. patrino phenotype data disease variants cause reference sequence blood group antigens
2 Most Recent Publications
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Control of peptide nanotube diameter by chemical modifications of an aromatic residue involved in a single close contact
(Article)
Tarabout, C. Roux, S. Buisson, D.A. Verbavatz, J.M. Petitjean, M. Valéry, C. Perrin, L. Rousseau, B. Artzner, F. Paternostre, M. Cintrat, J.C. Gobeaux, F. Fay, N. Pouget, E. Meriadec, C. Ligeti, M. Thomas, D. IJsselstijn, M. Besselievre, F. |
2011-05-10
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PhenCode: Connecting ENCODE data with mutations and phenotype
(Article)
Giardine, B. Riemer, C. Kern, A. Kuhn, R. Patrinos, G.P. Hughes, J. Higgs, D. Chui, D.H. Scriver, C.R. Phommarinh, M. Patnaik, S.K. Blumenfeld, O. Hefferon, T. Gottlieb, B. Vihinen, M. Väliaho, J. Kent, J. Miller, W. Hardison, R. Thomas, D. Hsu, F. Zielenski, J. Sang, Y. Elnitski, L. Cutting, G. Trumbower, H. |
2007-06-01
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