Kết quả tìm kiếm - Sandrine-Hélène Lefèvre
- Đang hiển thị 1 - 3 kết quả của 3
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1
Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas Bằng Nicolas Vogt, Sandrine-Hélène Lefèvre, Françoise Apiou, Anne‐Marie Dutrillaux, Andrej Cör, Pascal Leuraud, Marie‐France Poupon, Bernard Dutrillaux, Michelle Debatisse, Bernard Malfoy
Được phát hành 2004Artigo -
2
Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma Bằng Sophie Gad, Sandrine-Hélène Lefèvre, Sok Kean Khoo, Sophie Giraud, Annick Vieillefond, Viorel Vasiliu, Sophie Ferlicot, Vincent Molinié, Yves Denoux, Nicolas Thiounn, Yves Chrétien, A. Méjean, Marc Zerbib, G Benoît, J.M. Hervé, G Allègre, Brigitte Bressac–de Paillerets, Bin Tean Teh, Richard J. Kahnoski
Được phát hành 2006Artigo -
3
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma Bằng Betty Gardie, Audrey Remenieras, Darouna Kattygnarath, Johny Bombled, Sandrine-Hélène Lefèvre, Victoria Perrier-Trudova, Pierre Rustin, M. Barrois, Abdelhamid Slama, M.-F. Avril, D. Bessis, Olivier Caron, F. Caux, Patrick Collignon, I. Coupier, Catherine Cremin, Hélène Dollfus, Catherine Dugast, B. Escudier, Laurence Faivre, Michael Field, Brigitte Gilbert‐Dussardier, Nicolas Janin, Y. Leport, Dominique Leroux, Dan Lipsker, F. Malthieu, B. McGilliwray, Christine Maugard, A. Méjean, Isabelle Mortemousque, Ghislaine Plessis, Bruce Poppe, C. Pruvost‐Balland, S. Rooker, J. Roume, Nadem Soufir, M. Steinraths, Min Tan, Christine Théodore, L. Thomas, P. Vabres, E. Van Glabeke, Jean‐Baptiste Méric, Virginie Verkarre, Gilbert Lenoir, V. Joulin, Scott DeVeaux, Véronica Cusin, Jean Feunteun, Bin Tean Teh, Brigitte Bressac–de Paillerets, Richard J. Kahnoski
Được phát hành 2011Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
Cancer research
Medicine
Mutation
Pathology
Alu element
Amplicon
Cancer syndrome
Carcinoma
Chromophobe cell
Chromosome
Clear cell
DNA
Extrachromosomal DNA
Gene duplication
Gene mutation
Genome
Germline
Germline mutation
Human genome
Internal medicine
Kidney
Leiomyoma
Leiomyomatosis
Missense mutation
Molecular biology
Oncocytoma
Papillary renal cell carcinomas