A Novel System for the Quantification of the ADCC Activity of Therapeutic Antibodies

Autor: Christophe Lallemand, Feifei Liang, Flore Staub, Maud Simansour, Benoit Vallette, Lue Huang, Rosa Ferrando-Miguel, Michael G. Tovey

Publikováno v: Journal of Immunology Research, Vol 2017 (2017)

Novel ADCC effector cells expressing the V-variant or F-variant of FcγRIIIa (CD16a) and firefly luciferase under the control of a chimeric promoter incorporating recognition sequences for the principal transcription factors involved in FcγRIIIa sig

Externí odkaz: https://doaj.org/article/d64915da9b914ef28ce21a669e7787eb

GermlineSFTPA1mutation in familial idiopathic interstitial pneumonia and lung cancer

Autor: Serge Amselem, Alice De Ligniville, Dominique Valeyre, Nadia Nathan, Bruno Copin, Annick Clement, Nathalie Kuziner, Thierry Chinet, Valérie Nau, Florence Dastot-Le Moal, Raphael Borie, Clément Picard, Lamisse Mansour Hendili, Violaine Giraud, Hilario Nunes, Laurent Gouya, Aurore Coulomb, Louis-Jean Couderc, Bruno Crestani, Martine Reynaud Gaubert, Sylvie Tissier, Maud Simansour, Marie Legendre, Philippe Duquesnoy, Caroline Kannengiesser, Laurie Galeron

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, 2016, 25 (8), pp.1457-1467. ⟨10.1093/hmg/ddw014⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (8), pp.1457-1467. ⟨10.1093/hmg/ddw014⟩

Background: Idiopathic interstitial pneumonia (IIP) comprise a heterogeneous group of rare lung parenchyma disorders with high morbidity and mortality. They have been associated with an increased frequency of lung cancer. A genetic cause is identifie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::115e145c9af4b97be5795db26c4ecf04
https://doi.org/10.1093/hmg/ddw014

First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond–Blackfan anemia

Autor: Lydie, Da Costa, Genevieve, Chanoz-Poulard, Maud, Simansour, Martine, French, Raymonde, Bouvier, Fabienne, Prieur, Nathalie, Couque, Anne Lise, Delezoide, Thierry, Leblanc, Narla, Mohandas, Renaud, Touraine

Publikováno v: American journal of hematology. 88(4)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::82b67bf8a71088a623131b9b9dc319e5
https://pubmed.ncbi.nlm.nih.gov/23349008

Diamond-Blackfan anemia, ribosome and erythropoiesis

Autor: Hélène Moniz, Narla Mohandas, Maud Simansour, L. Da Costa, Thierry Leblanc, G. Tchernia

Publikováno v: Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 17(3)

Diamond-Blackfan anemia is a rare inherited bone marrow failure syndrome (five to seven cases per million live births) characterized by an aregenerative, usually macrocytic anemia with an absence or less than 5% of erythroid precursors (erythroblasto

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec58a92dbf8afdfb72eb5e046d1c4d9
https://pubmed.ncbi.nlm.nih.gov/20655265

Disorders of sex development and Diamond-Blackfan anemia: is there an association?

Autor: Brigitte Mignot, Anne-Marie Bertrand, Julia Hoefele, Thierry Leblanc, Martin Alberer, Maud Simansour, Lydie Da Costa, Gil Tchernia, Maximilian Stehr, Hans-Peter Schwarz

Publikováno v: Pediatric nephrology (Berlin, Germany). 25(7)

Diamond-Blackfan anemia (DBA) is a rare disorder characterized by congenital pure red cell aplasia. Mutations in ribosomal protein S19 (RPS19) have been identified in 25% of DBA patients. More recently, mutations in other ribosomal protein genes, nam

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c57aa0ca1b3460a591a91f4f66a2f714
https://pubmed.ncbi.nlm.nih.gov/20358230