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 TitleAuthors / EditorsDate
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A liver enhancer in the fibrinogen gene cluster Fort, Alexandre; Fish, Richard; Attanasio, Catia; Dosch, Roland; ... Neerman Arbez, Marguerite 2011
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A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis Robert-Ebadi, Helia; Le Querrec, Agnès; De Moerloose, Philippe; Gandon-Laloum, Sylvie; ... Neerman Arbez, Marguerite 2008
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A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite 2011
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A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream Robert-Ebadi, Helia; De Moerloose, Philippe; El Khorassani, M.; El Khattab, M.; Neerman Arbez, Marguerite 2009
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A novel regulatory element between the human FGA and FGG genes Fish, Richard; Neerman Arbez, Marguerite 2012
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Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T Attanasio, Catia; De Moerloose, Philippe; Antonarakis, Stylianos; Morris, Michael Andréw; Neerman Arbez, Marguerite 2001
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Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène Vu, Dung; Neerman Arbez, Marguerite 2006
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Apprentissage par problèmes des sciences médicales de base : les années précliniques (Bachelor) Baroffio Barbier, Anne; Neerman Arbez, Marguerite; Gallay, Christophe; Bernheim, Laurent 2011
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C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human Bontems, Franck; Fish, Richard; Rossitto-Borlat, Irène; Lembo, Frédérique; ... Lane, Lydie 2014
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Characterisation of a novel nonsense mutation in FGG (Fibrinogen Poznan) causing hypofibrinogenaemia with a mild bleeding tendency Zawilska, Krystyna; Undas, Anetta; Fish, R. J.; Molendowicz-Portala, Lucyna; ... Neerman Arbez, Marguerite 2010
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Clinical Consequences and Molecular Bases of Low Fibrinogen Levels Neerman Arbez, Marguerite; Casini, Alessandro 2018
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Clinical Features and Management of Congenital Fibrinogen Deficiencies Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite 2016
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Coexisting dysfibrinogenemia (gamma Arg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete) Travlou, A.; Gialeraki, A.; Merkouri, E.; Politou, M.; ... Neerman Arbez, Marguerite 2010
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Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient Farah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2006
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Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2003
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Congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2009
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Congenital fibrinogen disorders: an update De Moerloose, Philippe; Casini, Alessandro; Neerman Arbez, Marguerite 2013
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Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian Family Tchou, Isabelle; Neerman Arbez, Marguerite; Beris, Photis 2011
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Decreased plasmin resistance by clots of a homophenotypic Aalpha R 16H fibrinogen (Kingsport, slower fibrinopeptide A than fibrinopeptide B release) Galanakis, D. K.; Neerman Arbez, Marguerite; Kudryk, Bohdan; Henschen, Agnes 2010
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Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency Nyfeler, Beat; Kamiya, Yukiko; Boehlen, Françoise; Yamamoto, Kazuo; ... Neerman Arbez, Marguerite 2008
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Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia Neerman Arbez, Marguerite; Honsberger, A.; Antonarakis, Stylianos; Morris, Michael Andréw 1999
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Des-(27-31)C-peptide. A novel secretory product of the rat pancreatic beta cell produced by truncation of proinsulin connecting peptide in secretory granules Verchere, C. B.; Paoletta, M.; Neerman Arbez, Marguerite; Rose, Keith; ... Halban, Philippe A. 1996
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Developmental expression and organisation of fibrinogen genes in the zebrafish Fish, Richard; Vorjohann, Silja; Bena, Frédérique; Fort, Alexandre; Neerman Arbez, Marguerite 2012
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DNA Methylation Profiling of the Fibrinogen Gene Landscape in Human Cells and during Mouse and Zebrafish Development Vorjohann, Silja; Pitetti, Jean-Luc; Nef, Serge; Gonelle-Gispert, Carmen; ... Neerman Arbez, Marguerite 2013
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Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management Casini, Alessandro; Neerman Arbez, Marguerite; Ariëns, R A; De Moerloose, Philippe 2015
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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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FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations Casini, Alessandro; Lukowski, Samuel; Quintard, V Louvain; Crutu, A; ... Neerman Arbez, Marguerite 2014
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Fibrinogen and the risk of thrombosis De Moerloose, Philippe; Boehlen, Françoise; Neerman Arbez, Marguerite 2010
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Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis Rubbia-Brandt, Laura; Neerman Arbez, Marguerite; Rougemont, A. L.; Male, P. J.; Spahr, Laurent 2006
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Fibrinogen Gdansk: hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro) Mital, Andrzej; Undas, Anetta; Neerman Arbez, Marguerite; Hellmann, Andrzej 2012
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Fibrinogen gene mutations accounting for congenital afibrinogenemia Neerman Arbez, Marguerite 2001
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Fibrinogen gene regulation Fish, Richard; Neerman Arbez, Marguerite 2012
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Fibrinogen geneva II: a new congenitally abnormal fibrinogen alpha chain (Gly17Asp) with a review of similar mutations resulting in abnormal knob A. Casini, Alessandro; De Maistre, Emmanuel; Casini-Stuppi, Virginie; Fontana, Pierre; ... De Moerloose, Philippe 2014
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Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function Undas, Anetta; Zdziarska, Joanna; Iwaniec, Teresa; Stepien, Ewa; ... Neerman Arbez, Marguerite 2009
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Functional characterisation of plasma fibrin clots in Polish carriers of fibrinogen gammaArg275His mutation (fibrinogen Zabrze) Undas, Anetta; Pastuszczak, Maciej; Iwaniec, Teresa; Kapelak, Krystyna; Neerman Arbez, Marguerite 2010
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Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation Casini, Alessandro; Brungs, T; Lavenu-Bombled, C; Vilar, R; ... De Moerloose, Philippe 2017
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Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemia Tchou, Isabelle; Diepold, Myriam; Pilotto, P. A.; Swinkels, Dorine; ... Beris, Photis 2009
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Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis Tajdar, Mercedeh; Orlando, Christelle; Casini, Alessandro; Herpol, Margaux; ... Jochmans, Kristin 2017
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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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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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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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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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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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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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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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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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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 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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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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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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