Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Patricia Pasturaud"'
1
Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppression
Autor: G Linares-Cruz, Fabien Calvo, Marcel Tuynder, M Medhioub, H der Sarkissan, Lydie Bougueleret, D. Le Paslier, Robert Amson, Adam Telerman, Mona Nemani, Heriberto Bruzzoni-Giovanelli, F Sigaux, Veronique Alvaro, Daniel Cohen, Jean-Pierre Roperch, Patricia Pasturaud, Ilya Chumakov, Dorra Cherif, Moshe Oren, Jean Dausset, Lucien Cazes, I Le Gall, David Israeli
Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 1996, 93 (17), pp.9039-9042. ⟨10.1073/pnas.93.17.9039⟩
Proceedings of the National Academy of Sciences of the United States of America, 1996, 93 (17), pp.9039-9042. ⟨10.1073/pnas.93.17.9039⟩
International audience; Developmentally regulated genes in Drosophila, which are conserved through evolution, are potential candidates for key functions in biological processes such as cell cycle, programmed cell death, and cancer. We report cloning
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d189a11dc9e2f358062b4fcca26249e
https://doi.org/10.1073/pnas.93.17.9039
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2
A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene
Autor: Isabelle Richard, Jacques S. Beckmann, Charles Auffray, N. Chiannilkulchai, Patricia Pasturaud
Publikováno v: Human Molecular Genetics. 4:717-725
Previous genetic and physical studies of LGMD2A, an autosomal recessive form of limb-girdle muscular dystrophy, have led to the establishment of a 10-12 Mb YAC contig encompassing the morbid locus. In order to progress toward the identification of th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::080fee47761ec21d1d4f5c6eb421b238
https://doi.org/10.1093/hmg/4.4.717
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3
Specific association between alcohol intake, high grade of differentiation and 4q34-q35 deletions in hepatocellular carcinomas identified by high resolution allelotyping
Autor: Olivier Bluteau, Dominique Franco, Jean-Christophe Beaudoin, Paulette Bioulac-Sage, Jessica Zucman-Rossi, Pierre Laurent-Puig, Jacques Belghiti, Patricia Pasturaud
Publikováno v: Oncogene. 21(8)
One of the most frequent deletions in hepatocellular carcinoma (HCC) is that involving the long arm of chromosome 4 (30 to 70% of the cases). These chromosomal deletions are closely related to hepatitis B virus (HBV) infection. A tumor suppressor gen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::519fe4ad68cccc21be20dbd7169de539
https://pubmed.ncbi.nlm.nih.gov/11850842
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4
SIAH-1 promotes apoptosis and tumor suppression through a network involving the regulation of protein folding, unfolding, and trafficking: Identification of common effectors with p53 and p21Waf1
Autor: Robert Amson, Adam Telerman, Jean Dausset, Sylvie Prieur, Marcel Tuynder, Jean-Pierre Roperch, Patricia Pasturaud, David Israeli, Mona Nemani, Marie-Claude Gendron, Laurence Piouffre, Florence Lethrone, Moshe Oren
Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 1999, 96 (14), pp.8070-8073. ⟨10.1073/pnas.96.14.8070⟩
Proceedings of the National Academy of Sciences of the United States of America, 1999, 96 (14), pp.8070-8073. ⟨10.1073/pnas.96.14.8070⟩
We have previously described biological model systems for studying tumor suppression in which, by using H-1 parvovirus as a selective agent, cells with a strongly suppressed malignant phenotype (KS or US) were derived from malignant cell lines (K562
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211af7bd49155ccd2ae920f4bcaeda8c
https://hal.archives-ouvertes.fr/hal-02412845
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5
Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy
Autor: Patricia Pasturaud, Catherine Devaud, Isabelle Richard, O. Broux, Valérie Allamand, Anete Perelra de Souza, Lydle Brenguler, Hung Bui, Jacques S. Beckmann, Ilya Chumakov, Jean Welssenbach, Carinne Roudaut, Nathalie Bourg, Daniel Cohen, Françoise Fougerousse, N. Chiannilkulchai, Dominique Hillaire, Dorra Cherif
Publikováno v: Human molecular genetics. 3(2)
A gene responsible for an autosomal recessive form of limb girdle muscular dystrophy (LGMD2, MIM number 253600) has been localized on chromosome 15. After genotyping additional markers of this chromosome, two were found to flank the disease locus wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52c0ea80b4f24d83e80a8e3cea7a7a65
https://pubmed.ncbi.nlm.nih.gov/8004096
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8
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
Autor: L. Brenguier, Valéerie Allamand, Catherine Devaud, Odile Broux, Mayana Zatz, Carinne Roudaut, Patricia Pasturaud, Maria Rita Passos-Bueno, Jacques S. Beckmann, Michel Fardeau, Françoise Fougerousse, Charles E. Jackson, Daniel Cohen, Isabelle Richard, Nathalie Bourg, Jay A. Tischfield, N. Chiannilkulchai, Dominique Hillaire
Publikováno v: Cell. (1):27-40
Limb-girdle muscular dystrophies (LGMDs) are a group of inherited diseases whose genetic etiology has yet to be elucidated. The autosomal recessive forms (LGMD2) constitute a genetically heterogeneous group with LGMD2A mapping to chromosome 15815.1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::007c816e709bde0e6cd1d65cd41f6d50
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