Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Céline Duhamel"'
Autor:
Thibault Hirsch, Damien Neyens, Céline Duhamel, Alexandre Bayard, Christophe Vanhaver, Mathieu Luyckx, Francisco Sala de Oyanguren, Claude Wildmann, Nicolas Dauguet, Jean-Luc Squifflet, Virginie Montiel, Mélanie Deschamps, Pierre van der Bruggen
Publikováno v:
Cell Reports, Vol 43, Iss 7, Pp 114401- (2024)
Summary: Human CD8 tumor-infiltrating lymphocytes (TILs) with impaired effector functions and PD-1 expression are categorized as exhausted. However, the exhaustion-like features reported in TILs might stem from their activation rather than the conseq
Externí odkaz:
https://doaj.org/article/0f085d4caac14811beacbcd7a9577525
Autor:
Damien Neyens, Thibault Hirsch, Achraqat Abdel Aziz Issa Abdel Hadi, Nicolas Dauguet, Christophe Vanhaver, Alexandre Bayard, Claude Wildmann, Mathieu Luyckx, Jean-Luc Squifflet, Quentin D’Hondt, Céline Duhamel, Antoine Huaux, Virginie Montiel, Mélanie Dechamps, Pierre van der Bruggen
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionThe transcription factor HELIOS is primarily known for its expression in CD4 regulatory T cells, both in humans and mice. In mice, HELIOS is found in exhausted CD8 T cells. However, information on human HELIOS+ CD8 T cells is limited and
Externí odkaz:
https://doaj.org/article/1b8bb38eba084558be37214e1573ea67
Autor:
Simon Boussion, Sandra Whalen, Tania Attié-Bitach, Pierre-Simon Jouk, Dominique Carles, Sarah Grotto, Fabienne Escande, Florence Petit, Anne Bazin, Fanny Pelluard, Sylvie Manouvrier-Hanu, Louise Devisme, Perrine Brunelle, Yves Alembik, Céline Duhamel, Jamal Ghoumid, Thomas Smol, Charlotte Mechler, Alice Goldenberg, Laurence Loeuillet, Maryse Bonnière, Geneviève Baujat, Caroline Michot, Cyril Goizet, Philippe Carassou, Anne-Sophie Jourdain, Agnès Guichet, Audrey Putoux
Publikováno v:
Human mutationREFERENCES. 41(7)
Thrombocytopenia-absent radius (TAR) syndrome is characterized by radial defect and neonatal thrombocytopenia. It is caused by biallelic variants of RBM8A gene (1q21.1) with the association of a null allele and a hypomorphic noncoding variant. RBM8A