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 TitleAuthors / EditorsDate
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A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients Masternak, Krzysztof; Barras, Emmanuele; Zufferey, Madeleine; Conrad, Bernard; ... Reith, Walter 1998
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A highly recombinogenic system for the recovery of infectious Sendai paramyxovirus from cDNA: generation of a novel copy-back nondefective interfering virus Garcin, Dominique; Pelet, Thierry; Calain, Philippe; Roux, Laurent; ... Kolakofsky, Daniel 1995
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A role for the alphavbeta3 integrin in the transmigration of monocytes Weerasinghe, D.; McHugh, K. P.; Ross, F. P.; Brown, E. J.; ... Imhof, Beat 1998
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A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y Chen, H.; Rossier, Colette; Morris, Michael Andréw; Scott, Hamish Steele; ... Antonarakis, Stylianos 1999
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Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency Villard, Jean; Reith, Walter; Barras, Emmanuele; Gos, A.; ... Mach, Bernard 1997
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Cartography of methicillin-resistant S. aureus transcripts: detection, orientation and temporal expression during growth phase and stress conditions Beaume, Marie-Emilie; Hernandez, David; Farinelli, Laurent Luca Denis; Deluen, Cecile; ... Francois, Patrice 2010
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ChT1, an Ig superfamily molecule required for T cell differentiation Katevuo, K.; Imhof, Beat; Boyd, R.; Chidgey, A.; ... Vainio, O. 1999
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Cloning and functional characterization of mammalian homologues of the COPII component Sec23 Paccaud, Jean-Pierre; Reith, Walter; Carpentier, J. L.; Ravazzola, M.; ... Orci, Lelio 1996
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Cloning of a novel human neural cell adhesion molecule gene (NCAM2) that maps to chromosome region 21q21 and is potentially involved in Down syndrome Giacobino, Ariane; Chen, H.; Antonarakis, Stylianos 1997
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De novo generation of a non-segmented negative strand RNA virus with a bicistronic gene Touzelet, Olivier; Loukili, Noureddine; Pelet, Thierry; Fairley, Derek; ... Power, Ultan F. 2009
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Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene Hutter, P.; Antonarakis, Stylianos; Delozier-Blanchet, C. D.; Morris, Michael Andréw 1994
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Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients Abdel Wahab, Magy; De Moerloose, Philippe; Fish, R. J.; Neerman Arbez, Marguerite 2010
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Localization of 102 exons to a 2.5 Mb region involved in Down syndrome Lucente, D.; Chen, H. M.; Shea, D.; Samec, S. N.; ... McCormick, M. K. 1995
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Microbial surveillance during human pancreatic islet isolation Bucher, Pascal Alain Robert; Mathe, Zoltan; Bosco, Domenico; Oberholzer, José; ... Berney, Thierry 2004
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prdl-a, a gene marker for hydra apical differentiation related to triploblastic paired-like head-specific genes Gauchat-Feiss, Dominique Madeleine; Kreger, S; Holstein, T; Galliot, Brigitte 1998
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Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw 2003
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Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions Denoeud, France; Kapranov, Philipp; Ucla, Catherine; Frankish, Adam; ... Reymond, Alexandre 2007
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Renal and cardiac endothelial heterogeneity impact acute vascular rejection in pig-to-baboon xenotransplantation Knosalla, C.; Yazawa, K.; Behdad, A.; Bodyak, N.; ... Robson, S. C. 2009
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Splicing factor SF3a60 is the mammalian homologue of PRP9 of S.cerevisiae: the conserved zinc finger-like motif is functionally exchangeable in vivo Kraemer, Angela; Legrain, P; Mulhauser, Frank; Groening, Karsten Johannes; ... Bilbe, G 1994
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Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1) Roessler, E.; Mittaz, L.; Du, Y.; Scott, Hamish Steele; ... Antonarakis, Stylianos 1999
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The 21q22.1 STS marker, VN02 (EST00541 cDNA), is part of the 3' sequence of the human Na+/myo-inositol cotransporter (SLC5A3) gene Berry, G. T.; Mallee, J. J.; Blouin, Jean-Louis; Antonarakis, Stylianos 1996
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The hepatitis C virus core protein indirectly induces alpha-smooth muscle actin expression in hepatic stellate cells via interleukin-8 Clement, Sophie; Pascarella, Stephanie; Conzelmann, Stéphanie; Gonelle-Gispert, Carmen; ... Negro, Francesco 2010
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Two isoforms of a human intersectin (ITSN) protein are produced by brain-specific alternative splicing in a stop codon Guipponi, Michel; Scott, Hamish Steele; Chen, H.; Schebesta, A.; ... Antonarakis, Stylianos 1998