Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Marie-Genevieve Mattei"'
Autor:
James MUNDAY, Sheena KERR, Jian NI, Ann L. CORNISH, Jiquan Q. ZHANG, Gavin NICOLL, Helen FLOYD, Marie-Genevieve MATTEI, Paul MOORE, Ding LIU, Paul R. CROCKER
Publikováno v:
Biochemical Journal. 355:489-497
Here we characterize Siglec-10 as a new member of the Siglec family of sialic acid-binding Ig-like lectins. A full-length cDNA was isolated from a human spleen library and the corresponding gene identified. Siglec-10 is predicted to contain five extr
Autor:
Marie Genevieve Mattei, Marc Merten, Wafa Kammouni, Wanda Renaud, Françoise Birg, Catherine Figarella
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology. 15:520-528
Infection with the wild type SV40 virus was used to transform primary cultures of human tracheal gland serous (HTGS) cells. Over 80 different cell lines were obtained, but the majority had lost some of their epithelial and secretory features. However
Publikováno v:
Biochemistry. 33:15204-15214
Dipeptidyl peptidase IV (DPP IV, EC 3.4.14.5) is an ectopeptidase whose expression is modulated during thymocyte differentiation and T cell activation. We describe here the organization of the mouse DPP IV gene. This gene, which encompasses more than
Autor:
Kenneth S. Kurtz, Robert E. Burgeson, Marian E. Durkin, Reidar Albrechtsen, Ulla M. Wewer, Marie-France Champliaud, Marie-Genevieve Mattei, Donald R. Gerecke
Publikováno v:
Genomics. 24:243-252
Overlapping cDNA clones that encode the full-length human laminin beta 2 chain, formerly called the S chain, were isolated. The cDNA of 5680 nt contains a 5391-nt open reading frame encoding 1797 amino acids. At the amino terminus is a 32-amino-acid
Publikováno v:
Journal of Biological Chemistry. 269:7520-7526
To date, five distinct alpha chains have been identified in basement membrane collagen IV. We have cloned a gene encoding a new alpha chain belonging to basement membrane collagen IV by cDNA isolation under low stringency conditions. Isolation of ove
Autor:
Luis A. Diaz, Jouni Uitto, Mon-Li Chu, Daisuke Sawamura, George J. Giudice, Kehua Li, Marie Genevieve Mattei
Publikováno v:
Journal of Biological Chemistry. 266:24064-24069
We have recently isolated a 1.0-kilobase (kb) cDNA encoding 180-kDa bullous pemphigoid antigen (BPAG2), an autoantigen in blistering skin disease, bullous pemphigoid (Giudice, G. J., Squiquera, H. L., Elias, P. M., and Diaz, L. (1991) J. Clin. Invest
Autor:
Marc Delepine, Samuel F. Berkovic, Caroline Seegmuller, Pierre Cau, Nicolas Lévy, Danièle Depétris, Anne de Saint Martin, Marie-Genevieve Mattei, Nadine Bruneau, Ingrid E. Scheffer, Christian Marescaux, Bernd A. Neubauer, Andrée Robaglia-Schlupp, Annick Massacrier, Edouard Hirsch, Christophe Caloustian, Mark Lathrop, Rivka Ravid, Patrice Roll, Pierre Szepetowski, Elisabeth Flori, Marie-Noëlle Metz-Lutz, Maria-Paola Valenti, Sandrine Pereira, Gabrielle Rudolf, Christophe Beclin, Sarah Jamali, Arnaud Lemainque, Nathalie Roeckel-Trevisiol, Barbara Royer
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15(7), pp.1195-207
Human Molecular Genetics, 2006, 15(7), pp.1195-207
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15(7), pp.1195-207
Human Molecular Genetics, 2006, 15(7), pp.1195-207
The rolandic and sylvian fissures divide the human cerebral hemispheres and the adjacent areas participate in speech processing. The relationship of rolandic (sylvian) seizure disorders with speech and cognitive impairments is well known, albeit poor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f85126b537563dd3f0051e8ba377d8
https://hal.archives-ouvertes.fr/hal-00089725
https://hal.archives-ouvertes.fr/hal-00089725
Autor:
Hans R. Schöler, Roberto Di Lauro, Claudio Arra, Konstantinos Anastassiadis, Elio Biffali, Vincenzo Macchia, Angela Mariano, Catherine E. Ovitt, Alina Rodriguez-Mallon, Marie Genevieve Mattei, Paolo Emidio Macchia, Mario De Felice
Publikováno v:
ResearcherID
Alteration of thyroid gland morphogenesis (thyroid dysgenesis) is a frequent human malformation. Among the one in three to four thousand newborns in which congenital hypothyroidism is detected, 80% have either an ectopic, small and sublingual thyroid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::575be6a05c72e36f6d0c8cae9a8fdd47
http://hdl.handle.net/11588/149248
http://hdl.handle.net/11588/149248
Publikováno v:
Genomics. 16(3)
Autor:
Majambu Mbikay, Suzanne Benjannet, Marie Genevieve Mattei, Nabil G. Seidah, Laszlo Gaspar, M. Chrétien
Publikováno v:
Scopus-Elsevier
The chromosomal localization of the genes coding for the pro-protein and pro-hormone convertases PC1, PC2, and Furin has been achieved by in situ hybridization. The genes for PC1 and PC2 were located on human chromosomes 5q15-21 and 20p11.1-11.2, res