Zobrazeno 1 - 10
of 51
pro vyhledávání: '"E. Quelvennec"'
Publikováno v:
Tissue Antigens. 57:200-207
The Martinican population is mainly the product of admixture between African people and French Caucasians. The aim of the present study is to investigate at the DNA level the polymorphism of HLA class I (HLA-A, HLA-B) and class II (HLA-DRB1, DQB1 and
Autor:
Virginie Gandemer, E. Quelvennec, Patrice Poulain, J. Renouard, M. C. Laurent, G. Semana, E. Le Gall, Cécile Kaplan
Publikováno v:
British Journal of Haematology. 104:878-885
In a prospective study between 1993 and 1998, data was collected from 46 pregnant women and subsequently from their babies. 25 pregnant women with active autoimmune thrombocytopenic purpura (AITP) or a history of AITP (group A) and 21 pregnant women
Autor:
Michel Clanet, E Quelvennec, S. Eichenbaum, Françoise Clerget-Darpoux, Gilles Edan, M.-P. Roth, Gilbert Semana, J. Yaouanq
Publikováno v:
Science. 276:661-665
In their Perspective “The future of genetic studies of complex human diseases ([13 Sept., p. 1516][1]), Neil Risch and Kathleen Merikangas emphasize that such studies might benefit greatly from approaches based on gametic disequilibrium. Recent gen
Autor:
A. Parissiadis, Valérie Dubois, G. Dautin, Christophe Picard, C. Giannoli, Anne Cesbron, G. Semana, L. Absi, O. Toutirais, Virginie Renac, Françoise Hau, Florent Delbos, E. Quelvennec, Daniel Hanau
Publikováno v:
Transfusion Clinique et Biologique. 20:290-291
Autor:
G. Edan, E. Quelvennec, Gilbert Semana, Fabrice Jugdé, Mehdi Alizadeh, O. Bera, P. Cabre, D. Smadja
Publikováno v:
Tissue antigens. 61(2)
Among candidate genes involved in multiple sclerosis (MS) genetic susceptibility, MHC genes and particularly HLA-DRB1*1501–DQB1*0602 haplotype play a major role. Based on the strong linkage disequilibrium observed in Caucasians between DRB1*1501 an
Publikováno v:
Tissue antigens. 57(3)
The Martinican population is mainly the product of admixture between African people and French Caucasians. The aim of the present study is to investigate at the DNA level the polymorphism of HLA class I (HLA-A, HLA-B) and class II (HLA-DRB1, DQB1 and
Autor:
M N Bonnard, Y. Pawlotsky, Pascal Guggenbuhl, J Yaouanq, Gilbert Semana, Aleth Perdriger, E Quelvennec, Gérard Chalès
Publikováno v:
Rheumatology
Rheumatology, Oxford University Press (OUP), 1999, 38 (5), pp.448-52. ⟨10.1093/rheumatology/38.5.448⟩
Rheumatology, 1999, 38 (5), pp.448-52. ⟨10.1093/rheumatology/38.5.448⟩
Rheumatology, Oxford University Press (OUP), 1999, 38 (5), pp.448-52. ⟨10.1093/rheumatology/38.5.448⟩
Rheumatology, 1999, 38 (5), pp.448-52. ⟨10.1093/rheumatology/38.5.448⟩
Objective. HLA DM is a non-classical major histocompatibility complex (MHC) class II molecule that has been shown to facilitate peptide loading with classical class II molecules. Methods. In this study, we analysed the polymorphism in exon 3 of HLA D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f025c1ca8014fdd861c7801aeba7b106
https://hal.archives-ouvertes.fr/hal-00992068
https://hal.archives-ouvertes.fr/hal-00992068
Autor:
V, Gandemer, C, Kaplan, E, Quelvennec, P, Poulain, M C, Laurent, G, Semana, J, Renouard, E, Le Gall
Publikováno v:
British journal of haematology. 104(4)
In a prospective study between 1993 and 1998, data was collected from 46 pregnant women and subsequently from their babies. 25 pregnant women with active autoimmune thrombocytopenic purpura (AITP) or a history of AITP (group A) and 21 pregnant women
Autor:
S, Jean, E, Quelvennec, M, Alizadeh, P, Guggenbuhl, B, Birebent, A, Perdriger, B, Grosbois, P Y, Pawlotsky, G, Semana
Publikováno v:
Clinical and experimental rheumatology. 16(6)
Sjögren's syndrome (SS) is a chronic autoimmune disease with a genetic component. Among the genetic factors, the role of HLA class II genes has been suggested and a positive association with DRB1*03 allele has been described. However, there is no co
Autor:
D, Heresbach, A, Ababou, A, Bourienne, M, Alizadeh, E, Quelvennec, M, Pagenault, A, Dabadie, N H, Berre, J P, Campion, B, Launois, M, Gosselin, B, Genetet, J F, Bretagne, G, Semana
Publikováno v:
Gastroenterologie clinique et biologique. 21(8-9)
Multiplex family studies have excluded chromosome 6 as a candidate gene of susceptibility to inflammatory bowel disease. However, one recent study suggested that a gene involved in the pathogenesis of Crohn's disease is located on chromosome 6 confer