Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Emmanuel Collec"'
Autor:
Marine de Person, Thierry Billette de Villemeur, Lucie Dupuis, Fathi Moussa, Nadia Belmatoug, Emmanuel Collec, Nelly Reihani, Caroline Le Van Kim, Marc G. Berger, Mélanie Franco
Publikováno v:
American Journal of Hematology
American Journal of Hematology, Wiley, 2020, 95 (5), pp.483-491. ⟨10.1002/ajh.25744⟩
American Journal of Hematology, 2020, 95 (5), pp.483-491. ⟨10.1002/ajh.25744⟩
American Journal of Hematology, Wiley, 2020, 95 (5), pp.483-491. ⟨10.1002/ajh.25744⟩
American Journal of Hematology, 2020, 95 (5), pp.483-491. ⟨10.1002/ajh.25744⟩
Gaucher disease (GD) is a recessively inherited lysosomal storage disorder in which sphingolipids accumulates in the macrophages that transform into Gaucher cells. A growing body of evidence indicates that red blood cells (RBCs) represent important a
Autor:
Narla Mohandas, Xiuli An, Slim Azouzi, Caroline Le Van Kim, Emmanuel Collec, Yves Colin Aronovicz
Publikováno v:
British Journal of Haematology. 171:862-871
Introduction: Protein 4.1R is a cytoskeletal adaptor protein that is responsible for the control of the mechanical stability of erythrocyte membranes, and for the proper anchoring of transmembrane proteins to the membrane skeletal network. Analysis o
Autor:
Emmanuel Collec, Christiane Rose, Audrey Clapéron, Pierre Gane, Tanja Ouimet, Olivier F. Bertrand
Publikováno v:
Journal of Biological Chemistry. 280:21272-21283
The Kell blood group is a highly polymorphic system containing over 20 different antigens borne by the protein Kell, a 93-kDa type II glycoprotein that displays high sequence homology with members of the M13 family of zinc-dependent metalloproteases
Autor:
Jean-Pierre Cartron, Pierre Gane, Yves Colin, Emmanuel Collec, Wassim El Nemer, Caroline Le Van Kim
Publikováno v:
European Journal of Immunogenetics. 27:29-33
The McLeod syndrome is a rare X-linked recessive disorder characterized by blood group, neuromuscular and haematopoietic abnormalities. It is caused by XK gene defects and may include large deletions in the Xp21 region. Analysis of three unrelated Mc
Autor:
Jean-Pierre Cartron, Florence Carbonnet, Yves Colin, C. Le Van Kim, Emmanuel Collec, Olivier F. Bertrand, Claude Hattab
Publikováno v:
Immunogenetics. 50:16-21
The human Kx blood group antigen is carried by a 37,000 M(r) apparent molecular mass membrane polypeptide which is deficient in rare individuals with the McLeod syndrome. The X-linked human XK gene is transcribed in many tissues including adult skele
Autor:
Jean-Pierre Cartron, Emmanuel Collec, Olivier F. Bertrand, Caroline Le Van Kim, Florence Carbonnet, Claude Hattab
Publikováno v:
British Journal of Haematology. 96:857-863
The Kx protein is an erythrocyte membrane polypeptide which is deficient in rare individuals suffering from the McLeod syndrome. The gene encoding this protein has been recently cloned and the Kx protein independently purified as a covalent complex w
Autor:
Mélanie Franco, Philippe Connes, Emile van den Akker, Cyril Mignot, Thierry Billette de Villemeur, Marieke von Lindern, Yves Colin, Olivier Hermine, Emmanuel Collec, Nejma Ameziane, Nadia Belmatoug, Caroline Le Van Kim
Publikováno v:
Blood
Blood, American Society of Hematology, 2012, ?, pp.?-?
Blood, American Society of Hematology, 2013, 121, pp.546-555
Blood, 121(3), 546-555. American Society of Hematology
Blood, American Society of Hematology, 2012, ?, pp.?-?
Blood, American Society of Hematology, 2013, 121, pp.546-555
Blood, 121(3), 546-555. American Society of Hematology
Gaucher disease (GD) is a lysosomal storage disorder caused by glucocerebrosidase deficiency. It is notably characterized by splenomegaly, complex skeletal involvement, ischemic events of the spleen and bones, and the accumulation of Gaucher cells in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::782ea7a4e83e2133e4474985aa7f3562
https://hal.archives-ouvertes.fr/hal-00766815
https://hal.archives-ouvertes.fr/hal-00766815
Publikováno v:
Biochemical Journal
Biochemical Journal, Portland Press, 2011, 436 (3), pp.699-708. ⟨10.1042/BJ20101717⟩
Biochemical Journal, Portland Press, 2011, 436 (3), pp.699-708. ⟨10.1042/BJ20101717⟩
Lu/BCAM (Lutheran/basal cell-adhesion molecule) is a laminin 511/521 receptor expressed in erythroid and endothelial cells, and in epithelial tissues. The RK573–574 (Arg573-Lys574) motif of the Lu/BCAM cytoplasmic domain interacts with αI-spectrin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f36497c877cd2c84b158e2b077aabd0c
https://hal.archives-ouvertes.fr/hal-00596275/file/PEER_stage2_10.1042%2FBJ20101717.pdf
https://hal.archives-ouvertes.fr/hal-00596275/file/PEER_stage2_10.1042%2FBJ20101717.pdf
Autor:
Pierre Gane, Marie-Christine Lecomte, Didier Dhermy, Cécile Rahuel, Yves Colin, Emmanuel Collec, Wassim El Nemer, Caroline Le Van Kim, Jean-Pierre Cartron, Emilie Gauthier
Publikováno v:
Biochemical Journal
Biochemical Journal, Portland Press, 2006, 402 (2), pp.311-319. ⟨10.1042/BJ20060861⟩
Biochemical Journal, Portland Press, 2006, 402 (2), pp.311-319. ⟨10.1042/BJ20060861⟩
Lu (Lutheran) blood group and BCAM (basal cell adhesion molecule) antigens both reside on two gp (glycoprotein) isoforms, Lu and Lu(v13), that differ by the size of their cytoplasmic tail. They are receptors of laminin-10/11 and are expressed in RBCs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26e49d022fef228fe0eaa36c260f7c89
https://hal.archives-ouvertes.fr/hal-00478614
https://hal.archives-ouvertes.fr/hal-00478614
Publikováno v:
British journal of haematology. 93(2)
The Rh blood group antigens D, Cc and Ee are encoded by two related genes, RHD and RHCE. The RhG antigen (Rh12) is associated with the expression of RhC and/or RhD, except in rare variant red cells. Here we have determined the molecular basis of G ex