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Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III. Pietrys, Danuta; Balwierz, Walentyna; Iwaniec, Teresa; Vorjohann, Silja; ... Undas, Anetta 2011
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Treatment of congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2008
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To aggregate or not to aggregate Neerman Arbez, Marguerite 2007
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Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review Nagler, Michael; Kremer Hovinga, Johanna A; Alberio, Lorenzo; Peter-Salonen, Kristiina; ... Lämmle, Bernhard 2016
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Thromboelastographic phenotypes of fibrinogen and its variants: clinical and non-clinical implications Galanakis, Dennis K; Neerman Arbez, Marguerite; Brennan, Stephen; Rafailovich, Miriam; ... Scharrer, Inge 2014
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The molecular basis of inherited afibrinogenaemia Neerman Arbez, Marguerite 2001
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The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103 Neerman Arbez, Marguerite; Antonarakis, Stylianos; Blouin, Jean-Louis; Zeinali, S.; ... Tuddenham, E. G. 1997
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The GM2-1 ganglioside islet autoantigen in insulin-dependent diabetes mellitus is expressed in secretory granules and is not beta-cell specific Dotta, F.; Previti, M.; Neerman Arbez, Marguerite; Dionisi, S.; ... Halban, Philippe A. 1998
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The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster Neerman Arbez, Marguerite; Antonarakis, Stylianos; Honsberger, A.; Morris, Michael Andréw 1999
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Targeted mutation of zebrafish fga models human congenital afibrinogenemia Fish, Richard; Di Sanza, Corinne; Neerman Arbez, Marguerite 2014
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Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis Lebreton, A; Casini, Alessandro; Alhayek, R; Kouteich, K L; ... De Moerloose, Philippe 2015
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Slow cleavage at the proinsulin B-chain/connecting peptide junction associated with low levels of endoprotease PC1/3 in transformed beta cells Neerman Arbez, Marguerite; Sizonenko, S. V.; Halban, Philippe A. 1993
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Severe factor XI deficiency in a Lebanese family: identification of a novel missense mutation (Trp501Cys) in the catalytic domain De Moerloose, Philippe; Germanos-Haddad, Myrna; Boehlen, Françoise; Neerman Arbez, Marguerite 2004
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Severe bleeding and miscarriages in a hypofibrinogenemic woman heterozygous for the gamma Ala82Gly mutation Zdziarska, Joanna; Undas, Anetta; Basa, Joanna; Iwaniec, Teresa; ... Neerman Arbez, Marguerite 2009
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Regulation of fibrinogen production by microRNAs Fort, Alexandre; Borel, Christelle; Migliavacca, Eugenia; Antonarakis, Stylianos; ... Neerman Arbez, Marguerite 2010
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Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia Vu, Dung; Di Sanza, Corinne; Caille, Dorothee; De Moerloose, Philippe; ... Neerman Arbez, Marguerite 2005
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Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia Casini, Alessandro; Vilar, Rui; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite 2017
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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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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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Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: a systematic literature review Valiton, Vivian; Hugon-Rodin, Justine; Fontana, Pierre; Neerman Arbez, Marguerite; Casini, Alessandro 2019
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Novel, non-crinophagic, degradation of connecting peptide in transformed pancreatic beta cells Neerman Arbez, Marguerite; Halban, Philippe A. 1993
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Natural history of patients with congenital dysfibrinogenemia Casini, Alessandro; Blondon, Marc; Lebreton, Aurelien; Koegel, Jeremie; ... De Moerloose, Philippe 2015
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Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations Neerman Arbez, Marguerite; De Moerloose, Philippe 2007
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Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia Neerman Arbez, Marguerite; De Moerloose, Philippe; Bridel, C.; Honsberger, A.; ... Morris, Michael Andréw 2000
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Mutational epidemiology of congenital fibrinogen disorders Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite 2018
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Mutation of the translation initiation codon in FGA causes congenital afibrinogenemia Tirefort, Yordanka; Alson, Olivat Rakoto; De Moerloose, Philippe; Neerman Arbez, Marguerite 2012
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Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins Vu, Dung; Neerman Arbez, Marguerite 2007
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Molecular basis of fibrinogen deficiency Neerman Arbez, Marguerite 2006
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Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes Neerman Arbez, Marguerite; De Moerloose, Philippe; Honsberger, A.; Parlier, G.; ... Morris, Michael Andréw 2001
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Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency Neerman Arbez, Marguerite; Johnson, K. M.; Morris, Michael Andréw; McVey, J. H.; ... Tuddenham, E. G. 1999
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Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants Vu, Dung; Di Sanza, Corinne; Neerman Arbez, Marguerite 2008
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Loss of Dicer in Sertoli cells has a major impact on the testicular proteome of mice Papaioannou, Marilena D; Lagarrigue, Mélanie; Vejnar, Charles; Rolland, Antoine D; ... Nef, Serge 2011
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Local chromatin interactions contribute to expression of the fibrinogen gene cluster Espitia Jaimes, Cindy; Fish, Richard; Neerman Arbez, Marguerite 2018
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Levels of the conversion endoproteases PC1 (PC3) and PC2 distinguish between insulin-producing pancreatic islet beta cells and non-beta cells Neerman Arbez, Marguerite; Cirulli, V.; Halban, Philippe A. 1994
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Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders Neerman Arbez, Marguerite; De Moerloose, Philippe; Casini, Alessandro 2016
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Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes Lukowski, Samuel; Fish, Richard; Martin-Levilain, Juliette; Gonelle-Gispert, Carmen; ... Neerman Arbez, Marguerite 2015
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Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes Lukowski, Samuel; Fish, Richard; Martin-Levilain, Juliette; Gonelle-Gispert, Carmen; ... Neerman Arbez, Marguerite 2015
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Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects Miesbach, Wolfgang; Scharrer, Inge; Henschen, Agnes; Neerman Arbez, Marguerite; ... Galanakis, Dennis 2010
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Inactivation of AMMECR1 is associated with growth, bone, and heart alterations Moysés-Oliveira, Mariana; Giannuzzi, Giuliana; Fish, Richard; Rosenfeld, Jill A; ... Reymond, Alexandre 2018
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In vitro rescue of FGA deletion by lentiviral transduction of afibrinogenemic patient's hepatocytes Stroka, Deborah; Keogh, Adrian; Vu, Dung; Fort, Alexandre; ... Neerman Arbez, Marguerite 2014
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Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12 Friedli, Marc; Guipponi, Michel; Bertrand, Sonia; Bertrand, Daniel; ... Reymond, Alexandre 2003
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Identification of a novel F11 missense mutation (Ile463Ser) in a family with congenital factor XI deficiency Tirefort, Yordanka; Uhr, Mario R; Neerman Arbez, Marguerite; De Moerloose, Philippe 2012
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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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Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature Casini, Alessandro; Sokollik, C; Lukowski, Samuel; Lurz, E; ... Neerman Arbez, Marguerite 2015
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Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion Vu, Dung; De Moerloose, Philippe; Batorova, A.; Lazur, J.; ... Neerman Arbez, Marguerite 2005
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Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob 'A' Vorjohann, Silja; Fish, Richard; Biron-Andreani, Christine; Nagaswami, Chandrasekaran; ... Neerman Arbez, Marguerite 2010
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Human proinsulin conversion in the regulated and the constitutive pathways of transfected AtT20 cells Irminger, Jean-Claude; Vollenweider, F. M.; Neerman Arbez, Marguerite; Halban, Philippe A. 1994
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Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiency Germanos-Haddad, Myrna; De Moerloose, Philippe; Boehlen, Françoise; Peyvandi, Flora; Neerman Arbez, Marguerite 2005
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Homophenotypic Aalpha R16H fibrinogen (Kingsport): uniquely altered polymerization associated with slower fibrinopeptide A than fibrinopeptide B release Galanakis, D. K.; Neerman Arbez, Marguerite; Scheiner, Tomas; Henschen, Agnes; ... Weisel, J. W. 2007
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High incidence of ectopic nucleolar organizer regions in human testicular tumors Neerman Arbez, Marguerite; Delozier-Blanchet, C. D.; Bolle, J. F.; Rondez, R.; Morris, Michael Andréw 1993
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