Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Melissa Mathieu"'
Autor:
Annie Reynolds, Joanne Berghout, Irena Kirillova, John B. Wallingford, Pierre Drapeau, Jonathan R. McDearmid, Zoha Kibar, Elena Torban, Melissa Mathieu, Patrizia De Marco, Julie M. Hayes, Elisa Merello, Philippe Gros, Valeria Capra
Publikováno v:
New England Journal of Medicine. 356:1432-1437
Neural-tube defects such as anencephaly and spina bifida constitute a group of common congenital malformations caused by complex genetic and environmental factors. We have identified three mutations in the VANGL1 gene in patients with familial types
Publikováno v:
Blood Cells, Molecules, and Diseases. 35:212-216
DMT1 (Nramp2, Slc11a2) mediates iron uptake at the intestinal brush border and across the membrane of acidified endosomes. A single patient with severe microcytic anemia and iron overload was recently reported to carry a mutation in exon 12 of DMT1 (
Autor:
Mélissa Mathieu, Natacha Cotta-Grand, Jean-François Daudelin, Salix Boulet, Réjean Lapointe, Nathalie Labrecque
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30139 (2012)
The identification of the signals that should be provided by antigen-presenting cells (APCs) to induce a CD8(+) T cell response in vivo is essential to improve vaccination strategies using antigen-loaded APCs. Although dendritic cells have been exten
Externí odkaz:
https://doaj.org/article/91e852c2b4a5496db91c145bf8a29c82