Kết quả tìm kiếm - Barbier, Mathieu
- Đang hiển thị 1 - 7 kết quả của 7
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1
Response to Park et al. Bằng Barbier, Mathieu, Davoine, Claire Sophie, Brice, Alexis, Durr, Alexandra
Được phát hành 2021Text -
2
CD1 Gene Polymorphisms and Phenotypic Variability in X-Linked Adrenoleukodystrophy Bằng Barbier, Mathieu, Sabbagh, Audrey, Kasper, Edwige, Asheuer, Muriel, Ahouansou, Ornella, Pribill, Ingrid, Forss-Petter, Sonja, Vidaud, Michel, Berger, Johannes, Aubourg, Patrick
Được phát hành 2012Text -
3
Gene expression analysis reveals early changes in several molecular pathways in cerebral malaria-susceptible mice versus cerebral malaria-resistant mice Bằng Delahaye, Nicolas F, Coltel, Nicolas, Puthier, Denis, Barbier, Mathieu, Benech, Philippe, Joly, Florence, Iraqi, Fuad A, Grau, Georges E, Nguyen, Catherine, Rihet, Pascal
Được phát hành 2007Text -
4
Platelets Alter Gene Expression Profile in Human Brain Endothelial Cells in an In Vitro Model of Cerebral Malaria Bằng Barbier, Mathieu, Faille, Dorothée, Loriod, Béatrice, Textoris, Julien, Camus, Claire, Puthier, Denis, Flori, Laurence, Wassmer, Samuel Crocodile, Victorero, Geneviève, Alessi, Marie-Christine, Fusaï, Thierry, Nguyen, Catherine, Grau, Georges E., Rihet, Pascal
Được phát hành 2011Text -
5
Factors influencing the age at onset in familial frontotemporal lobar dementia: Important weight of genetics Bằng Barbier, Mathieu, Camuzat, Agnès, Houot, Marion, Clot, Fabienne, Caroppo, Paola, Fournier, Clémence, Rinaldi, Daisy, Pasquier, Florence, Hannequin, Didier, Pariente, Jérémie, Larcher, Kathy, Brice, Alexis, Génin, Emmanuelle, Sabbagh, Audrey, Le Ber, Isabelle
Được phát hành 2017Text -
6
Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias Bằng Fournier, Clémence, Anquetil, Vincent, Camuzat, Agnès, Stirati-Buron, Sandrine, Sazdovitch, Véronique, Molina-Porcel, Laura, Turbant, Sabrina, Rinaldi, Daisy, Sánchez-Valle, Raquel, Barbier, Mathieu, Latouche, Morwena, Stevanin, Giovanni, Seilhean, Danielle, Brice, Alexis, Duyckaerts, Charles, Le Ber, Isabelle
Được phát hành 2018Text -
7
MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections Bằng Barbier, Mathieu, Gross, Marie-Sylvie, Aubart, Mélodie, Hanna, Nadine, Kessler, Ketty, Guo, Dong-Chuan, Tosolini, Laurent, Ho-Tin-Noe, Benoit, Regalado, Ellen, Varret, Mathilde, Abifadel, Marianne, Milleron, Olivier, Odent, Sylvie, Dupuis-Girod, Sophie, Faivre, Laurence, Edouard, Thomas, Dulac, Yves, Busa, Tiffany, Gouya, Laurent, Milewicz, Dianna M., Jondeau, Guillaume, Boileau, Catherine
Được phát hành 2014Text