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 TitleAuthors / EditorsDate
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Trans-splicing mutants of Chlamydomonas reinhardtii Goldschmidt-Clermont, Michel P.; Girard, Jacqueline; Choquet, Yves Marcel; Rochaix, Jean-David 1990
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A unique chicken B-creatine kinase gene gives rise to two B-creatine kinase isoproteins with distinct N termini by alternative splicing Wirz, T; Brändle, U; Soldati, Thierry; Hossle, J P; Perriard, J C 1990
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Chloroplast ribosomal intron of Chlamydomonas reinhardtii: in vitro self-splicing, DNA endonuclease activity and in vivo mobility Duerrenberger, Franz; Rochaix, Jean-David 1991
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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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Essential domains of the PRP21 splicing factor are implicated in the binding to PRP9 and PRP11 proteins and are conserved through evolution Rain, J C; Tartakoff, A M; Kraemer, Angela; Legrain, P 1996
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Mammalian splicing factor SF1 is encoded by variant cDNAs and binds to RNA Backes, Silke; Gruter, Patric Gerold; Bilbe, Graeme; Kraemer, Angela 1996
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Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1) Lalioti, M. D.; Mirotsou, M.; Buresi, C.; Peitsch, M. C.; ... Antonarakis, Stylianos 1997
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Expression of leptin receptor mRNA (long form splice variant) in the human cerebellum Savioz, Armand; Charnay, Yves; Huguenin, C; Graviou, Christelle; ... Bouras, Constantin 1997
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Coordination of Nuclear and Chloroplast Gene Expression in Plant Cells Goldschmidt-Clermont, Michel P. 1997
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Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester storage disease in unrelated compound heterozygous and hemizygous individuals Ries, S; Büchler, C; Schindler, G; Aslanidis, C; ... Schmitz, G 1998
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Conservation of functional domains involved in RNA binding and protein-protein interactions in human and Saccharomyces cerevisiae pre-mRNA splicing factor SF1 Rain, J C; Rafi, Zahra; Rhani, Zakaria; Legrain, P; Kraemer, Angela 1998
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Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia Savioz, Armand; Kovari, Eniko Veronika; Anastasiu, R; Rossier, Colette; ... Leuba, G 2000
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mRNA export: travelling with DEAD box proteins Linder, Patrick; Stutz, Françoise 2001
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Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA) Attanasio, Catia; David, Armelle; Neerman Arbez, Marguerite 2003
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Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells Neerman Arbez, Marguerite; Germanos-Haddad, Myrna; Tzanidakis, Konstantinos; Vu, Dung; ... De Moerloose, Philippe 2004
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Cellular viral rebound after cessation of potent antiretroviral therapy predicted by levels of multiply spliced HIV-1 RNA encoding nef Fischer, Marek; Joos, Beda; Hirschel, Bernard; Bleiber, Gabriela; ... Gunthard, Huldrych 2004
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Human splicing factor SF3a, but not SF1, is essential for pre-mRNA splicing in vivo Tanackovic Abbas-Terki, Goranka; Kraemer, Angela 2005
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Structure-function analysis of the U2 snRNP-associated splicing factor SF3a Kraemer, Angela; Ferfoglia, Fabio; Huang, Ching-Jung; Mulhaupt, Flore; ... Tanackovic Abbas-Terki, Goranka 2005
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DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects Hornef, Nada; Olbrich, Heike; Horvath, Judit; Zariwala, M. A.; ... Omran, Heymut 2006
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Molecular basis of fibrinogen deficiency Neerman Arbez, Marguerite 2006
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