Zobrazeno 1 - 10
of 953
pro vyhledávání: '"GRANDCHAMP, B"'
Publikováno v:
In Solid State Electronics 2011 57(1):67-72
Autor:
Vuillaumier-Barrot, S., Bouchet-Seraphin, C., Chelbi, M., Eude-Caye, A., Charluteau, E., Besson, C., Quentin, S., Devisme, L., Le Bizec, C., Landrieu, P., Goldenberg, A., Maincent, K., Loget, P., Boute, O., Gilbert-Dussardier, B., Encha-Razavi, F., Gonzales, M., Grandchamp, B., Seta, N.
Publikováno v:
In Neuromuscular Disorders 2011 21(11):782-790
Autor:
Van Den Daele, W., Augendre, E., Le Royer, C., Damlencourt, J.-F., Grandchamp, B., Cristoloveanu, S.
Publikováno v:
In Solid State Electronics February 2010 54(2):205-212
Autor:
Romanjek, K., Augendre, E., Van Den Daele, W., Grandchamp, B., Sanchez, L., Le Royer, C., Hartmann, J.-M., Ghyselen, B., Guiot, E., Bourdelle, K., Cristoloveanu, S., Boulanger, F., Clavelier, L.
Publikováno v:
In Microelectronic Engineering 2009 86(7):1585-1588
Autor:
Grandchamp, B., Picat, C., Mignotte, V., Wilson, J. H. P., Velde, K. Te, Sandkuyl, L., Roméo, P. H., Goossens, M., Nordmann, Y.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1989 Jan . 86(2), 661-664.
Externí odkaz:
https://www.jstor.org/stable/33186
Publikováno v:
In Solid State Electronics June 2005 49(6):956-964
Autor:
Ibarrola-Villava M, Kumar R, Nagore E, Benfodda M, Guedj M, Gazal S, Hu HH, Guan J, Rachkonda PS, Descamps V, Basset-Seguin N, Bensussan A, Bagot M, Saiag P, Schadendorf D, Martin-Gonzalez M, Mayor M, Grandchamp B, Ribas G, Soufir N
Publikováno v:
INTERNATIONAL JOURNAL OF CANCER
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Multifactorial predisposition to melanoma includes genes involved in pigmentation, immunity and DNA repair. Nonetheless, missing heritability in melanoma is still important. We studied the role of 335 candidate SNPs in melanoma susceptibility by usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::95af33f74b738f1bc4a0c2a283280bbe
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1258
https://www.fundanet.incliva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1258
Autor:
Campagna, D.R., Bie, C.I. De, Schmitz-Abe, K., Sweeney, M., Sendamarai, A.K., Schmidt, P.J., Heeney, M.M., Yntema, H.G., Kannengiesser, C., Grandchamp, B., Niemeyer, C.M., Knoers, N.V.A.M., Swart, S., Marron, G., Wijk, R. van, Raymakers, R.A.P., May, A., Markianos, K., Bottomley, S.S., Swinkels, D.W., Fleming, M.D.
Publikováno v:
American Journal of Hematology, 89, 3, pp. 315-9
American Journal of Hematology, 89(3), 315-319. Wiley
American Journal of Hematology, 89, 315-9
American Journal of Hematology, 89(3), 315-319. Wiley
American Journal of Hematology, 89, 315-9
Contains fulltext : 137231.pdf (Publisher’s version ) (Open Access) X-linked sideroblastic anemia (XLSA) is the most common form of congenital sideroblastic anemia. In affected males, it is uniformly associated with partial loss-of-function missens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::43ab8da268bd4f2c357a1bf34806e7b1
https://hdl.handle.net/2066/137231
https://hdl.handle.net/2066/137231
Publikováno v:
Molecular Membrane Biology. 16:305-312
Hereditary spherocytosis (HS), a common human inherited haemolytic anaemia, is associated with partial deficiency of different erythrocyte membrane proteins. In a subset of dominant HS, a partial membrane expression deficiency of band 3, the erythroc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbabb96f7a45843b24d25522fc6e21f0
https://doi.org/10.1080/096876899294526
https://doi.org/10.1080/096876899294526