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Urokinase-type plasminogen activator and its receptor synergize to promote pathogenic proteolysis Zhou, Hong-Ming; Nichols, Anthony; Meda, Paolo; Vassalli, Jean-Dominique 2000
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The TATA-binding protein-associated factor yTafII19p functionally interacts with components of the global transcriptional regulator Ccr4-Not complex and physically interacts with the Not5 subunit Lemaire, Marc; Collart, Martine 2000
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The essential function of Not1 lies within the Ccr4-Not complex Maillet, Laurent Jean Marie; Tu, Chi; Hong, Y K; Shuster, E O; Collart, Martine 2000
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Both transmembrane domains of SecG contribute to signal sequence recognition by the Escherichia coli protein export machinery Bost, S.; Silva, Filo; Rudaz, C.; Belin, Dominique 2000
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Expression of an activated Notch4(int-3) oncoprotein disrupts morphogenesis and induces an invasive phenotype in mammary epithelial cells in vitro Soriano, Jesus; Uyttendaele, Hendrik; Kitajewski, Jan; Montesano, Roberto 2000
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Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases Ferreiro, A; Estournet, B; Chateau, D; Romero, N B; ... Fardeau, M 2000
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Heterologously expressed Staphylococcus aureus fibronectin-binding proteins are sufficient for invasion of host cells Sinha, B.; Francois, Patrice; Que, Y. A.; Hussain, M.; ... Herrmann, M. 2000
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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
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Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency Bartoloni, Lucia; Wattenhofer, M.; Kudoh, J.; Berry, A.; ... Antonarakis, Stylianos 2000
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Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity Blouin, Jean-Louis; Meeks, M.; Radhakrishna, U.; Sainsbury, A.; ... Antonarakis, Stylianos 2000
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Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome Chrast, R.; Scott, Hamish Steele; Madani, Rime; Huber, L.; ... Antonarakis, Stylianos 2000
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Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychological and language phenotypes Eliez, Stéphan; Palacio-Espasa, Francisco; Spira, A.; Lacroix, M.; ... Cramer, B. 2000
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Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes Pulver, A. E.; Mulle, J.; Nestadt, G.; Swartz, K. L.; ... McGrath, J. A. 2000
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Cultured arterial smooth muscle cells maintain distinct phenotypes when implanted into carotid artery Bochaton-Piallat, Marie-Luce; Clowes, A. W.; Clowes, M. M.; Fischer, J. W.; ... Gabbiani, Giulio 2001
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Mitogen-activated protein kinase phosphatase is required for genotoxic stress relief in Arabidopsis Ulm, Roman; Revenkova, E.; di Sansebastiano, G. P.; Bechtold, N.; Paszkowski, Jerzy 2001
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Primary immunodeficiency mutation databases Vihinen, M.; Arredondo-Vega, F. X.; Casanova, J. L.; Etzioni, A.; ... Smith, C. I. 2001
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Patterns of engraftment in different strains of immunodeficient mice reconstituted with human peripheral blood lymphocytes Berney, Thierry; Molano, R D; Pileggi, A; Cattan, P; ... Inverardi, L 2001
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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
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Fibrinogen gene mutations accounting for congenital afibrinogenemia Neerman Arbez, Marguerite 2001
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Directed inhibition of nuclear import in cellular hypertrophy Perez-Terzic, Carmen; Gacy, A. M.; Bortolon, R.; Dzeja, P. P.; ... Terzic, A. 2001
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Accuracy of two-dimensional electrophoresis for target discovery in human colorectal cancer Ott, Vincent Olivier; Guenther, K; Steinert, R; Tortola, S; ... Reymond, M A 2001
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In vivo emergence of subpopulations expressing teicoplanin or vancomycin resistance phenotypes in a glycopeptide-susceptible, methicillin-resistant strain of Staphylococcus aureus Vaudaux, Pierre; Francois, Patrice; Berger-Bachi, B.; Lew, Daniel Pablo 2001
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Chromosome 21: from sequence to applications Antonarakis, Stylianos 2001
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Differential gene expression studies to explore the molecular pathophysiology of Down syndrome Antonarakis, Stylianos; Lyle, Robert; Chrast, R.; Scott, Hamish Steele 2001
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Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia Bartoloni, Lucia; Blouin, Jean-Louis; Maiti, A. K.; Sainsbury, A.; ... Antonarakis, Stylianos 2001
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Beta-cell-targeted expression of a dominant-negative hepatocyte nuclear factor-1 alpha induces a maturity-onset diabetes of the young (MODY)3-like phenotype in transgenic mice Hagenfeldt-Johansson, K. A.; Herrera, Pedro Luis; Wang, Haiyan; Gjinovci, A.; ... Wollheim, Claes 2001
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Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposis Hutter, Pierre; Rey-Berthod, C; Chappuis, Pierre; Couturier, A; ... Soravia, Claudio 2001
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Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains Wattenhofer, M.; Shibuya, K.; Kudoh, J.; Lyle, Robert; ... Scott, Hamish Steele 2001
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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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Depletion of MOM1 in non-dividing cells of Arabidopsis plants releases transcriptional gene silencing Tariq, Muhammad; Habu, Yoshiki; Paszkowski, Jerzy 2002
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Two regulatory levels of transcriptional gene silencing in Arabidopsis Mittelsten Scheid, Ortrun; Probst, Aline V.; Afsar, Karin; Paszkowski, Jerzy 2002
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A new gene in Drosophila melanogaster, Ravus, the phantom of the modifier of position-effect variegation Su(var)3-7 Delattre, Marion; Spierer, Anne; Hulo, Nicolas; Spierer, Pierre 2002
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Interaction between Not1p, a component of the Ccr4-not complex, a global regulator of transcription, and Dhh1p, a putative RNA helicase Maillet, Laurent Jean Marie; Collart, Martine 2002
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Effect of rosiglitazone on the differential expression of diabetes-associated proteins in pancreatic islets of C57Bl/6 lep/lep mice Sanchez, Jean-Charles; Converset, Véronique; Nolan, Anna; Schmid, Gerhard; ... Cawthorne, Michael A 2002
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Calreticulin reveals a critical Ca(2+) checkpoint in cardiac myofibrillogenesis Li, Jian; Puceat, Michel; Perez-Terzic, Carmen; Mery, Annabelle; ... Jaconi, Marisa 2002
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A point mutant of GAP-43 induces enhanced short-term and long-term hippocampal plasticity Hulo, S.; Alberi, Stefano; Laux, T.; Muller, Dominique; Caroni, P. 2002
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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Ferreiro-girani, Ana; Monnier, Nicole; Romero, Norma B; Leroy, Jean-Paul; ... Guicheney, Pascale 2002
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Increased expression of clumping factor and fibronectin-binding proteins by hemB mutants of Staphylococcus aureus expressing small colony variant phenotypes Vaudaux, Pierre; Francois, Patrice; Bisognano, Carmelo; Kelley, William; ... Von Eiff, Christof 2002
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Analysis of HIV-1- and CMV-specific memory CD4 T-cell responses during primary and chronic infection Harari, Alexandre; Rizzardi, G. P.; Ellefsen, Kim; Ciuffreda, Donatella; ... Pantaleo, Giuseppe 2002
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Defective insulin secretion in pancreatic beta cells lacking type 1 IGF receptor Xuan, Shouhong; Kitamura, Tadahiro; Nakae, Jun; Politi, Katerina; ... Efstratiadis, Argiris 2002
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Autoantibodies to fibroblasts induce a proadhesive and proinflammatory fibroblast phenotype in patients with systemic sclerosis Chizzolini, Carlo; Raschi, Elena; Rezzonico, Roger Michel; Testoni, Cinzia; ... Meroni, Pier Luigi 2002
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Arterial smooth muscle cell heterogeneity: implications for atherosclerosis and restenosis development Hao, Hiroyuki; Gabbiani, Giulio; Bochaton-Piallat, Marie-Luce 2003
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Testis determination requires insulin receptor family function in mice Nef, Serge; Verma-Kurvari, Sunita; Merenmies, Jussi; Vassalli, Jean-Dominique; ... Parada, Luis F. 2003
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TGFbeta directs gene expression of activated microglia to an anti-inflammatory phenotype strongly focusing on chemokine genes and cell migratory genes Paglinawan, Rey; Malipiero, Ursula; Schlapbach, Ralph; Frei, Karl; ... Fontana, Adriano 2003
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A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24 de Mollerat, X. J.; Gurrieri, Fiorella; Morgan, C. T.; Sangiorgi, Eugenio; ... Schwartz, C. E. 2003
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Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome Deutsch, Samuel; Rideau, Alexandra; Bochaton-Piallat, Marie-Luce; Merla, Giuseppe; ... Beris, Photis 2003
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Acquired and reversible Pelger-Huët anomaly of polymorphonuclear neutrophils in three transplant patients receiving mycophenolate mofetil therapy Asmis, Lars; Hadaya, Karine; Majno, Pietro; Toso, Christian; ... Starobinski, Michel 2003
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Plasminogen mediates the pathological effects of urokinase-type plasminogen activator overexpression Bolon, Isabelle; Zhou, Hong-Ming; Charron, Yves; Wohlwend, Annelise Isabelle; Vassalli, Jean-Dominique 2004
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Formation of multivesicular endosomes in Dictyostelium Marchetti, Anna; Mercanti, Valentina; Cornillon, Sophie Marie; Alibaud, Laethitia; ... Cosson, Pierre 2004
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Phenotypic heterogeneity of dopa-responsive dystonia in monozygotic twins Grötzsch, H; Schnorf, H; Morris, M A; Moix, Isabelle; ... Burkhard, Pierre 2004
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