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A member of a new VH gene family encodes antibromelinized mouse red blood cell autoantibodies Reininger, Luc; Kaushik, A.; Izui, Shozo; Jaton, J. C. 1988
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A two-step recognition of signal sequences determines the translocation efficiency of proteins Belin, Dominique; Bost, S.; Vassalli, Jean-Dominique; Strub, K. 1996
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Agenesis of human pancreas due to decreased half-life of insulin promoter factor 1 Schwitzgebel Luscher, Valérie; Mamin, Aline; Brun, Thierry; Ritz, Beate Andréa; ... Philippe, Jacques 2003
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Alternative ribosomal initiation gives rise to chicken brain-type creatine kinase isoproteins with heterogeneous amino termini Soldati, Thierry; Schäfer, B W; Perriard, J C 1990
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An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree Radhakrishna, U.; Senol, S.; Herken, H.; Gucuyener, K.; ... Antonarakis, Stylianos 2001
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An integrated encyclopedia of DNA elements in the human genome ENCODE Project Consortium 2012
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Analysis of TAP2 and HLA-DP gene polymorphism in psoriasis Fakler, J. W.; Schmitt-Egenolf, M.; Vejbaesya, S.; Boehncke, Wolf-Henning; ... Eiermann, T. H. 1994
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Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically Blouin, Jean-Louis; Binkert, F.; Antonarakis, Stylianos 1994
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Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse Rajput, B.; Marshall, A.; Killary, A. M.; Lalley, P. A.; ... Strickland, S. 1987
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Dependence of position-effect variegation in Drosophila on dose of a gene encoding an unusual zinc-finger protein Reuter, Gunter; Giarre, Marianna; Farah, Joseph; Gausz, Janos; ... Spierer, Pierre 1990
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Disease-causing mutations in the human genome Antonarakis, Stylianos; Krawczak, M.; Cooper, D. N. 2000
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DNA typing by microbead arrays and PCR-SSP: apparent false-negative or -positive hybridization or amplification signals disclose new HLA-B and -DRB1 alleles Rahal, M.; Kervaire, B.; Villard, Jean; Tiercy, Jean-Marie 2008
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Dominant-negative effects of a novel mutated Ins2 allele causes early-onset diabetes and severe beta-cell loss in Munich Ins2C95S mutant mice Herbach, Nadja; Rathkolb, Birgit; Kemter, Elisabeth; Pichl, Lisa; ... Wanke, Ruediger 2007
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Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1 Cironi, Luisa; Provero, Paolo; Riggi, Nicola; Janiszewska, Michalina; ... Stamenkovic, Ivan 2009
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Frequency of replication/transcription errors in (A)/(T) runs of human genes Giacobino, Ariane; Rossier, Colette; Papasavvas, M.; Antonarakis, Stylianos 2001
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Genes and loops in 320,000 base-pairs of the Drosophila melanogaster chromosome Mirkovitch, Jovan; Spierer, Pierre; Laemmli, Ulrich K. 1986
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Genetic implication of a novel thiamine transporter in human hypertension International Consortium for Blood Pressure Genome-Wide Association Studies 2014
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Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee White, J. A.; McAlpine, P. J.; Antonarakis, Stylianos; Cann, H.; ... Povey, S. 1997
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Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes Chen, H.; Lowther, W.; Avramopoulos, D.; Antonarakis, Stylianos 1994
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Inducible and irreversible control of gene expression using a single transgene Fuhrmann-Benzakein, Edya; Garcia, Irène; Pepper, Michael Sean; Vassalli, Jean-Dominique; Herrera, Pedro Luis 2000
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