Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Françoise Dorion-Bonnet"'
Autor:
Lois M. Mulligan, Harriet Feilotter, J L McVeigh, Charis Eng, Bernadette Duboué, Valérie Coulon, Françoise Dorion-Bonnet, Alexander Boag, Michel Longy, W C W Latham
Publikováno v:
British Journal of Cancer
We examined a panel of sporadic breast carcinomas for loss of heterozygosity (LOH) in a 10-cM interval on chromosome 10 known to encompass the PTEN gene. We detected allele loss in 27 of 70 breast tumour DNAs. Fifteen of these showed loss limited to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ba1022ebad4552fe130debf2b18f22f
https://doi.org/10.1038/sj.bjc.6690115
https://doi.org/10.1038/sj.bjc.6690115
Autor:
Rosalind A. Eeles, Valérie Coulon, Michel Longy, H. Christian Weber, Katherine M. Call, Anne Louise Richardson, Bruce G. Robinson, Zimu Zheng, Shirley Hodgson, Françoise Dorion-Bonnet, Deborah J. Marsh, Patricia L. M. Dahia, Charis Eng, Albert Y. Lin, Alisa M. Goldstein, Randall Little
Publikováno v:
Genes, Chromosomes and Cancer. 21:61-69
Cowden disease (CD) is a rare, autosomal dominant inherited cancer syndrome characterized by multiple benign and malignant lesions in a wide spectrum of tissues. While individuals with CD have an increased risk of breast and thyroid neoplasms, the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c2e801acd90ca57618be2f1680c8281
https://doi.org/10.1002/(sici)1098-2264(199801)21:1<61::aid-gcc8>3.0.co
https://doi.org/10.1002/(sici)1098-2264(199801)21:1<61::aid-gcc8>3.0.co
Autor:
Sergey Shaposhnikov, Henning Johansen, Michel Longy, Françoise Dorion-Bonnet, Kaja Klykken Aas, Hans Prydz, Jim Thorsen, Martin Krekling, Laurence Taine, Delfine Lafon, Christophe Bepoldin, Azza Abd El Monéim, Philippe Rocca-Serra, Eirik Frengen
Publikováno v:
Genomics. 70(3)
Loss of heterozygosity (LOH) on the long arm of human chromosome 16 is a common genetic alteration observed in both invasive ductal and invasive lobular breast carcinomas. We have generated a high-resolution integrated map encompassing the smallest r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::103590e4d91d7296e89d269332908402
https://pubmed.ncbi.nlm.nih.gov/11161777
https://pubmed.ncbi.nlm.nih.gov/11161777
Autor:
Sergey Shaposhnikov, Philippe Rocca-Serra, Michel Longy, Eirik Frengen, Hans Prydz, Françoise Dorion-Bonnet, C Bépoldin, Jim Thorsen, Laurence Taine
Publikováno v:
Europe PubMed Central
Breast Cancer Research : BCR
Breast Cancer Research : BCR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4cb0b0e6c355fb3b01434354e8c26ca
https://doi.org/10.1186/bcr165
https://doi.org/10.1186/bcr165
Autor:
Keltouma Driouch, Michel Longy, Rosette Lidereau, Marie-Hélène Champème, Marianne Briffod, Françoise Dorion-Bonnet
Publikováno v:
Genes, chromosomescancer. 19(3)
One of the main genetic abnormalities associated with breast carcinogenesis is the loss of genetic material from chromosome arm 16q. Different groups have identified two regions (16q22.1 and 16q24-ter) that are frequently deleted in primary tumors, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6015bfa8275b20dee7726093fbb7bd91
https://pubmed.ncbi.nlm.nih.gov/9219000
https://pubmed.ncbi.nlm.nih.gov/9219000
Autor:
Sergey Shaposhnikov, Azza Abd El Moneim, Hans Prydz, Laurence Taine, Michel Longy, Jim Thorsen, Françoise Dorion-Bonnet, Philippe Rocca-Serra, Eirik Frengen
Publikováno v:
Nature Genetics. 27:54-54
A high-resolution integrated map of the breast cancer loss of heterozygosity region on human chromosome 16q22.1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38d73d0a5ca6e24d77400d69a9e18929
https://doi.org/10.1038/87080
https://doi.org/10.1038/87080