Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nadine Gruson"'
Autor:
Stéphanie Struski, Martine Doco‐Fenzy, Michael Koehler, Ilse Chudoba, Francis Levy, Linda Masson, Nicole Michel, Evelyne Ulrich, Nadine Gruson, Jean Bénard, Gérard Potron, Pascale Cornillet‐Lefebvre
Publikováno v:
Analytical Cellular Pathology, Vol 25, Iss 3, Pp 115-122 (2003)
In order to identify genomic changes associated with a resistant phenotype acquisition, we used comparative genomic hybridization (CGH) to compare a human ovarian cell line, Igrov1, and four derived subcell lines, resistant to vincristine and present
Externí odkaz:
https://doaj.org/article/3d2ef34cd2634cf7bb930c91d0f6e39a
Autor:
Stéphanie Struski, Nadine Gruson, Martine Doco-Fenzy, Nicole Michel, Linda Masson, Jean Dufer, Evelyne Ulrich, Gérard Potron, Pascale Cornillet-Lefebvre
Publikováno v:
Cancer Genetics and Cytogenetics. 132:51-54
In order to identify genomic changes associated with drug-resistance acquisition, we performed R-banding karyotyping, fluorescence in situ hybridization, and comparative genomic hybridization to compare a human T-cell lymphoblastic leukemia cell line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9119353f313b083623ff21c02078238
https://doi.org/10.1016/s0165-4608(01)00519-2
https://doi.org/10.1016/s0165-4608(01)00519-2
Autor:
Linda Masson, Martine Doco-Fenzy, Pascale Cornillet-Lefebvre, Marylène Proult, Stéphanie Struski, Nadine Gruson, Evelyne Ulrich, Gérard Potron, Aurélie Trussardi, Jean-Claude Jardillier
Publikováno v:
Genes, Chromosomes and Cancer. 30:136-142
In order to identify genomic changes associated with an etoposide resistance acquisition, we used comparative genomic hybridization (CGH) to compare a human lung adenocarcinoma cell line, A549 wild type, and three sublines, A549-VP1-3, exposed to inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b21b9e5cc32be6a056544bb473780851
https://doi.org/10.1002/1098-2264(2000)9999:9999<::aid-gcc1071>3.0.co
https://doi.org/10.1002/1098-2264(2000)9999:9999<::aid-gcc1071>3.0.co
Autor:
Martine Doco-Fenzy, Celine Poirsier, Nathalie Bednarek, Jean-Marie Nobecourt, Nadine Gruson, Maroun Khoury, Christelle Manjeongean, Nicole Michel, Patrice Morville, Sandrine Clomes, Pascal Schmidt, Anita Riot, Dominique Gaillard, Emilie Landais
Publikováno v:
European journal of medical genetics. 57(5)
The duplication of the short arm (p) of chromosome 12 is a rare chromosomal abnormality, and most reported cases result from malsegregation of a balanced parental translocation associated with other chromosomal imbalances. Of the reported cases, only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57a4aeb3f43d4a5ae814c2c560ebf6aa
https://pubmed.ncbi.nlm.nih.gov/24503147
https://pubmed.ncbi.nlm.nih.gov/24503147