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 TitleAuthors / EditorsDate
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 Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A Lakich, D.; Kazazian, H. H.; Antonarakis, Stylianos; Gitschier, J. 1993
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 TGF-beta 1 influences the relative development of the exocrine and endocrine pancreas in vitro Sanvito, F.; Herrera, Pedro Luis; Huarte, Joachim; Nichols, A.; ... Vassalli, Jean-Dominique 1994
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 Dinucleotide repeat polymorphism within ERCC5 gene Samec, S.; Clarkson, S. G.; Blaschak, J.; Chakravarti, A.; ... Antonarakis, Stylianos 1994
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 The large subunit of HIV-1 reverse transcriptase interacts with beta-actin Hottiger, M.; Gramatikoff, K.; Georgiev, O.; Chaponnier, Christine; ... Hubscher, U. 1995
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 Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A. 1995
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 Identification of the ligand-binding domain of the surface-located fibrinogen receptor (clumping factor) of Staphylococcus aureus McDevitt, D.; Francois, Patrice; Vaudaux, Pierre; Foster, T. J. 1995
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 The 5' ends of Hantaan virus (Bunyaviridae) RNAs suggest a prime-and-realign mechanism for the initiation of RNA synthesis Garcin, Dominique; Lezzi, M; Dobbs, M; Elliott, R M; ... Kolakofsky, Daniel 1995
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 Use of Amplified Fragment Length Polymorphism in Molecular Typing of Legionella pneumophila and Application to Epidemiological Studies Valsangiacomo, Claudio; Baggi, Franca; Gaia, Valeria; Balmelli, Tiziano; ... Piffaretti, Jean-Claude 1995
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 The rat hepatic leukemia factor (HLF) gene encodes two transcriptional activators with distinct circadian rhythms, tissue distributions and target preferences Falvey, Eileen Elisabeth; Fleury Olela, Fabienne; Schibler, Ulrich 1995
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 Transgenic analysis of a potential Hoxd-11 limb regulatory element present in tetrapods and fish Beckers, Johannes; Gerard, Matthieu; Duboule, Denis 1996
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 The human lanosterol synthase gene maps to chromosome 21q22.3 Young, M.; Chen, H.; Lalioti, M. D.; Antonarakis, Stylianos 1996
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 The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3 Lalioti, M. D.; Gos, A.; Green, M. R.; Rossier, Colette; ... Antonarakis, Stylianos 1996
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 YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome Nadal, M.; Mila, M.; Pritchard, M.; Mur, A.; ... Estivill, X. 1996
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 Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21 Blouin, Jean-Louis; Duriaux Sail, Geneviève; Chen, H.; Gos, A.; ... Antonarakis, Stylianos 1996
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 A low-fibronectin-binding mutant of Staphylococcus aureus 879R4S has Tn918 inserted into its single fnb gene Greene, C.; Vaudaux, Pierre; Francois, Patrice; Proctor, R. A.; ... Foster, T. J. 1996
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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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 Isolation of a human gene (HES1) with homology to an Escherichia coli and a zebrafish protein that maps to chromosome 21q22.3 Scott, Hamish Steele; Chen, H.; Rossier, Colette; Lalioti, M. D.; Antonarakis, Stylianos 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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 PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy Guicheney, P; Vignier, N; Zhang, X; He, Y; ... Tryggvason, K 1998
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 An improved method for isolation of microvascular endothelial cells from normal and inflamed human lung Lou, Jinning; Mili, Nabil; Decrind, Christophe Jean-Yves; Donati, Yves Richard; ... Grau, Georges 1998
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