Show items per page
Elements: 276
Page 1 on 6
 TitleAuthors / EditorsDate
add to browser selection
Normal phenotype with paternal uniparental isodisomy for chromosome 21 Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos 1993
add to browser selection
Soluble and cell-bound forms of steel factor activity play distinct roles in melanocyte precursor dispersal and survival on the lateral neural crest migration pathway Wehrle-Haller, Bernhard; Weston, J A 1995
add to browser selection
Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia Rogan, P. K.; Close, P.; Blouin, Jean-Louis; Seip, J. R.; ... Antonarakis, Stylianos 1995
add to browser selection
An in vivo pathway for disulfide bond isomerization in Escherichia coli Rietsch, A.; Belin, Dominique; Martin, N.; Beckwith, J. 1996
add to browser selection
Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus Karayiorgou, M.; Gogos, J. A.; Galke, B. L.; Jeffery, J. A.; ... Pulver, A. E. 1996
add to browser selection
The Johns Hopkins University Collaborative Schizophrenia Study: an epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes Pulver, A. E.; Wolyniec, P. S.; Housman, D.; Kazazian, H. H.; ... Kempf, L. 1996
add to browser selection
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
add to browser selection
Identification of HLA-DR and -DQ alleles conferring susceptibility to pollen allergy and pollen associated food allergy Boehncke, Wolf-Henning; Loeliger, C.; Kuehnl, P.; Kalbacher, H.; ... Gall, H. 1998
add to browser selection
Genotype-phenotype correlations in attenuated adenomatous polyposis coli Soravia, Claudio; Berk, T; Madlensky, L; Mitri, A; ... Bapat, B 1998
add to browser selection
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
add to browser selection
IgM anti-hepatitis C virus core antibodies as marker of recurrent hepatitis C after liver transplantation Negro, Francesco; Giostra, Emiliano; Rubbia-Brandt, Laura; Mentha, Gilles; ... Hadengue, Antoine 1998
add to browser selection
Randomized, placebo-controlled, double-blind trial to evaluate the efficacy of mupirocin for eradicating carriage of methicillin-resistant Staphylococcus aureus Harbarth, Stéphan Juergen; Dharan, S.; Liassine, N.; Herrault, Pascale; ... Pittet, Didier 1999
add to browser selection
Mutation analyses of North American APS-1 patients Heino, M.; Scott, Hamish Steele; Chen, Q.; Peterson, P.; ... Krohn, K. 1999
add to browser selection
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21 Antonarakis, Stylianos; Blouin, Jean-Louis; Lasseter, V. K.; Gehrig, Corinne; ... Pulver, A. E. 1999
add to browser selection
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations Radhakrishna, U.; Bornholdt, D.; Scott, Hamish Steele; Patel, U. C.; ... Antonarakis, Stylianos 1999
add to browser selection
Impact of drug resistance mutations on virologic response to salvage therapy. Swiss HIV Cohort Study Lorenzi, P.; Opravil, M.; Hirschel, Bernard; Chave, J. P.; ... Yerly Ferrillo, Sabine 1999
add to browser selection
Endogenous targets of transcriptional gene silencing in Arabidopsis Steimer, A.; Amedeo, P.; Afsar, K.; Fransz, P.; ... Paszkowski, Jerzy 2000
add to browser selection
Hepatitis C virus, the E2 envelope protein, and alpha-interferon resistance Abid, Karim; Quadri Defilippis, Rafael; Negro, Francesco 2000
add to browser selection
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping Kibar, Z.; Dube, M. P.; Powell, J.; McCuaig, C.; ... Rouleau, G. A. 2000
add to browser selection
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III Levinson, D. F.; Holmans, P.; Straub, R. E.; Owen, M. J.; ... Mallet, J. 2000
add to browser selection
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD) Maiti, A. K.; Bartoloni, Lucia; Mitchison, H. M.; Meeks, M.; ... Antonarakis, Stylianos 2000
add to browser selection
Hepatocyte steatosis is a cytopathic effect of hepatitis C virus genotype 3 Rubbia-Brandt, Laura; Quadri Defilippis, Rafael; Abid, Karim; Giostra, Emiliano; ... Negro, Francesco 2000
add to browser selection
A novel hepatitis C virus (HCV) subtype from Somalia and its classification into HCV clade 3 Abid, Karim; Quadri Defilippis, Rafael; Veuthey, Anne-Lise; Hadengue, Antoine; Negro, Francesco 2000
add to browser selection
Primary immunodeficiency mutation databases Vihinen, M.; Arredondo-Vega, F. X.; Casanova, J. L.; Etzioni, A.; ... Smith, C. I. 2001
add to browser selection
A worldwide analysis of AG molecular diversity inferred from serology Sanchez-Mazas, Alicia; Bütler-Brunner, E.; Bütler, R.; Calderón, R.; ... Langaney, André 2001
add to browser selection
Donor- and ligand-dependent differences in C-C chemokine receptor 5 reexpression Sabbe, Rebecca; Picchio, Gastón R; Pastore, Cristina; Chaloin, Olivier; ... Mosier, Donald E 2001
add to browser selection
The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes Bruneau, Sylvia; Johnson, Kenneth R.; Yamamoto, Masakazu; Kuroiwa, Atsushi; Duboule, Denis 2001
add to browser selection
Fibrinogen gene mutations accounting for congenital afibrinogenemia Neerman Arbez, Marguerite 2001
add to browser selection
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness Masmoudi, S.; Antonarakis, Stylianos; Schwede, T.; Ghorbel, A. M.; ... Guipponi, Michel 2001
add to browser selection
Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study Eliez, Stéphan; Antonarakis, Stylianos; Morris, Michael Andréw; Dahoun, S. P.; Reiss, A. L. 2001
add to browser selection
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
add to browser selection
Nosocomial outbreak of multiple bloodborne viral infections Yerly Ferrillo, Sabine; Quadri Defilippis, Rafael; Negro, Francesco; Posfay Barbe, Klara; ... Perrin, Luc 2001
add to browser selection
Liver disease in pediatric patients with cystic fibrosis is associated with glutathione S-transferase P1 polymorphism Henrion-Caude, Alexandra; Flamant, Cyril; Roussey, Michel; Housset, Chantal; ... Clement, Annick 2002
add to browser selection
Chronic graft dysfunction in renal transplant patients: potential role of plasminogen activator inhibitor type 1 Lahlou, Anis; Peraldi, Marie-Noelle; Thervet, Eric; Flahault, Antoine; ... Rondeau, Eric 2002
add to browser selection
Kjellin's syndrome: fundus autofluorescence, angiographic, and electrophysiologic findings Frisch, Inez B; Haag, Peter; Steffen, Heimo; Weber, Bernhard H F; Holz, Frank G 2002
add to browser selection
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro Guipponi, Michel; Vuagniaux, Gregoire; Wattenhofer, Marie; Shibuya, Kazunori; ... Rossier, B. C. 2002
add to browser selection
Testis determination requires insulin receptor family function in mice Nef, Serge; Verma-Kurvari, Sunita; Merenmies, Jussi; Vassalli, Jean-Dominique; ... Parada, Luis F. 2003
add to browser selection
Genetic and environmental risk factors for oral anticoagulant overdose Verstuyft, C.; Robert, A.; Morin, S.; Loriot, Marie-Anne; ... Becquemont, L. 2003
add to browser selection
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia Lewis, C. M.; Blouin, Jean-Louis; Antonarakis, Stylianos 2003
add to browser selection
Specific BACE1 genotypes provide additional risk for late-onset Alzheimer disease in APOE epsilon 4 carriers Gold, Gabriel; Blouin, Jean-Louis; Herrmann, François; Michon, Agnès; ... Antonarakis, Stylianos 2003
add to browser selection
Failures of 1 week on, 1 week off antiretroviral therapies in a randomized trial Ananworanich, Jintanat; Nuesch, Reto; Le Braz, Michelle; Chetchotisakd, Ploechan; ... Yerly Ferrillo, Sabine 2003
add to browser selection
PSC-RANTES blocks R5 human immunodeficiency virus infection of Langerhans cells isolated from individuals with a variety of CCR5 diplotypes Kawamura, Tatsuyoshi; Bruce, Shannon E; Abraha, Awet; Sugaya, Makoto; ... Blauvelt, Andrew 2004
add to browser selection
Structure of Pseudomonas aeruginosa populations analyzed by single nucleotide polymorphism and pulsed-field gel electrophoresis genotyping Morales, Gracia; Wiehlmann, Lutz; Gudowius, Peter; Van Delden, Christian; ... Rojo, Fernando 2004
add to browser selection
Characterization of cell-to-cell signaling-deficient Pseudomonas aeruginosa strains colonizing intubated patients Denervaud, Valerie; TuQuoc, Patrick; Blanc, Dominique; Favre-Bonte, Sabine Adelaide Eugenie; ... Van Delden, Christian 2004
add to browser selection
Association of the connexin36 gene with juvenile myoclonic epilepsy Mas, Christophe; Taske, N.; Deutsch, Samuel; Guipponi, Michel; ... Meda, Paolo 2004
add to browser selection
Pax2 mutant mice display increased number and size of islets of Langerhans but no change in insulin and glucagon content Zaiko, Maia; Estreicher, Anne; Ritz-Laser, Beate; Herrera, Pedro Luis; ... Philippe, Jacques 2004
add to browser selection
Codeine intoxication associated with ultrarapid CYP2D6 metabolism Gasche, Yvan; Daali, Youssef; Fathi, Marc; Chiappe, Alberto; ... Desmeules, Jules Alexandre 2004
add to browser selection
Infrequent transmission of HIV-1 drug-resistant variants Yerly Ferrillo, Sabine; Jost, Stéphanie; Telenti, Amalio; Flepp, Markus; ... Perrin, Luc 2004
add to browser selection
The Ccr4-Not complex independently controls both Msn2-dependent transcriptional activation--via a newly identified Glc7/Bud14 type I protein phosphatase module--and TFIID promoter distribution Lenssen, Eve; James, Nicole; Pedruzzi, Ivo; Dubouloz, Frédérique; ... De Virgilio, Claudio 2005
add to browser selection
Use of an automated multiple-locus, variable-number tandem repeat-based method for rapid and high-throughput genotyping of Staphylococcus aureus isolates Francois, Patrice; Huyghe, Antoine; Charbonnier, Yvan; Bento, Manuela; ... Schrenzel, Jacques 2005
<< previous | 1 | 2 | 3 | 4 | 5 | 6 |