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INFRAFRONTIER quality principles in systemic phenotyping.
Mamm Genome. 2022 Mar;33(1):120-122. doi: 10.1007/s00335-021-09892-2. Epub 2021 Jul 30.
Mamm Genome. 2022.
PMID: 34328547
Free PMC article.
Review.
Rapid in vivo analysis of mutant forms of the LAT adaptor using Pax5-Lat double-deficient pro-B cells.
Ardouin L, Rolink AG, Mura AM, Gommeaux J, Melchers F, Busslinger M, Malissen M, Malissen B.
Ardouin L, et al. Among authors: mura am.
Eur J Immunol. 2005 Mar;35(3):977-86. doi: 10.1002/eji.200425836.
Eur J Immunol. 2005.
PMID: 15719364
Free article.
Item in Clipboard
Induction of T helper type 2 immunity by a point mutation in the LAT adaptor.
Aguado E, Richelme S, Nuñez-Cruz S, Miazek A, Mura AM, Richelme M, Guo XJ, Sainty D, He HT, Malissen B, Malissen M.
Aguado E, et al. Among authors: mura am.
Science. 2002 Jun 14;296(5575):2036-40. doi: 10.1126/science.1069057.
Science. 2002.
PMID: 12065839
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Linker for activation of T cells integrates positive and negative signaling in mast cells.
Malbec O, Malissen M, Isnardi I, Lesourne R, Mura AM, Fridman WH, Malissen B, Daëron M.
Malbec O, et al. Among authors: mura am.
J Immunol. 2004 Oct 15;173(8):5086-94. doi: 10.4049/jimmunol.173.8.5086.
J Immunol. 2004.
PMID: 15470052
Free article.
Item in Clipboard
LAT regulates gammadelta T cell homeostasis and differentiation.
Nuñez-Cruz S, Aguado E, Richelme S, Chetaille B, Mura AM, Richelme M, Pouyet L, Jouvin-Marche E, Xerri L, Malissen B, Malissen M.
Nuñez-Cruz S, et al. Among authors: mura am.
Nat Immunol. 2003 Oct;4(10):999-1008. doi: 10.1038/ni977. Epub 2003 Sep 14.
Nat Immunol. 2003.
PMID: 12970761
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T cell development and T cell responses in mice with mutations affecting tyrosines 292 or 315 of the ZAP-70 protein tyrosine kinase.
Magnan A, Di Bartolo V, Mura AM, Boyer C, Richelme M, Lin YL, Roure A, Gillet A, Arrieumerlou C, Acuto O, Malissen B, Malissen M.
Magnan A, et al. Among authors: mura am.
J Exp Med. 2001 Aug 20;194(4):491-505. doi: 10.1084/jem.194.4.491.
J Exp Med. 2001.
PMID: 11514605
Free PMC article.
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Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
Arimura T, Helbling-Leclerc A, Massart C, Varnous S, Niel F, Lacène E, Fromes Y, Toussaint M, Mura AM, Keller DI, Amthor H, Isnard R, Malissen M, Schwartz K, Bonne G.
Arimura T, et al. Among authors: mura am.
Hum Mol Genet. 2005 Jan 1;14(1):155-69. doi: 10.1093/hmg/ddi017. Epub 2004 Nov 17.
Hum Mol Genet. 2005.
PMID: 15548545
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