Výsledky vyhledávání - "Fabienne Kerangueven"

Integrated Map of the Chromosome 8p12–p21 Region, a Region Involved in Human Cancers and Werner Syndrome

Autor: L Essioux, Max Chaffanet, T Noguchi, A Imbert, M.-J. Pébusque, Fabienne Kerangueven, David Jérémie Birnbaum, Catherine Bonaïti-Pellié, José Adélaïde, Hagay Sobol, D Le Paslier

Publikováno v: Genomics. 32:29-38

Detailed physical maps of the human genome are important resources for the identification and isolation of disease genes and for studying the structure and function of the genome. To improve the definition of the 8p12-p21 chromosomal region, an integ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08233eb474cb12c95f7506c13eaf985f
https://doi.org/10.1006/geno.1996.0073

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Multiple sites of loss of heterozygosity on chromosome arms 3p and 3q in human breast carcinomas

Autor: Jeannine Geneix, Véronique Wargniez, David Jérémie Birnbaum, Charles Theillet, T Noguchi, Jocelyne Jacquemier, Florence Allione, Hagay Sobol, Fabienne Kerangueven

Publikováno v: Europe PubMed Central

Loss of heterozygosity (LOH) at loci from both arms of chromosome 3 were shown to occur in a high proportion of breast carcinomas. Six regions of consistent loss were identified, and were variably involved in the tumors. This suggests that multiple p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e74e60edd7621dd9c9255acc7e855e2
https://pubmed.ncbi.nlm.nih.gov/21594365

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Genome-wide search for loss of heterozygosity in Burkitt lymphoma cell lines

Autor: Giovanni Romeo, Luo Yin, Daniel Birnbaum, Suzanne Pauly, Tetsuro Noguchi, Hagay Sobol, Gilbert M. Lenoir, Athmane Benziane, Fabienne Kerangueven, François Eisinger, Michel Longy

Publikováno v: Genes, chromosomescancer. 33(2)

The molecular biological characteristics of Burkitt lymphoma (BL), in addition to the presence of the Epstein-Barr virus (EBV) in some forms, relies on well-characterized alterations, such as MYC translocations and TP53 inactivations. To ascertain th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c7de500f5cd0625fea609999408d7e9
https://pubmed.ncbi.nlm.nih.gov/11793449

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Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions

Autor: Tetsuro Noguchi, Georges Padberg, François Eisinger, Daniel Birnbaum, Fabienne Kerangueven, Michel Longy, Véronique Wargniez, Charles Theillet, Charis Eng, Jocelyne Jacquemier, Florence Allione, Hagay Sobol

Publikováno v: Oncogene, 14, 3, pp. 339-347
Oncogene, 14, 339-347
Scopus-Elsevier

To appreciate the involvement of known or potential susceptibility genes in sporadic breast tumors, we have searched for chromosomal deletions by studying loss of heterozygosity (LOH) at 43 microsatellite (CA)n markers from human chromosomes 10, 11 a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::389a9a129300dc4b03870546106b7890
https://repository.ubn.ru.nl/handle/2066/265532

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Cumulative regional allelotyping of human breast carcinomas

Autor: François Eisinger, Fabienne Kerangueven, Véronique Wargniez, Jocelyne Jacquemier, David Jérémie Birnbaum, Hagay Sobol, Florence Allione, T Noguchi, Patricia Parc

Publikováno v: Europe PubMed Central

We have analyzed losses of heterozygosity (LOH) at markers from chromosomes 1, 2, 4 and 5 in a panel of 53 consecutive breast carcinomas. Together with a parallel analysis of LOH at chromosome 3, this allowed the identification of twenty-one regions

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3d144ef18903ba2dc0ba64f12b1a005
https://doi.org/10.3892/ijo.8.6.1155

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Patterns of loss of heterozygosity at loci from chromosome arm 13q suggests a possible involvement of BRCA2 in sporadic breast tumors

Autor: Jocelyne Jacquemier, Fabienne Kerangueven, Daniel Birnbaum, Florence Allione, Hagay Sobol, José Adélaïde, Teburo Noguchi

Publikováno v: Genes, chromosomescancer. 13(4)

Loss of heterozygosity (LOH) at loci from chromosome I3 is frequently observed in breast cancer. Chromosome 13 contains at least two cancer genes, the well-characterized RB1 gene located at 13q 14 and the breast cancer-susceptibility gene, BRCA2, rec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a786206bd18b162cb1df2e40bda46870
https://pubmed.ncbi.nlm.nih.gov/7547638

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ALLELIC LOSS AT MARKERS OF CHROMOSOMAL BAND 7Q31 IS NOT A FREQUENT EVENT IN HUMAN BREAST-CANCER

Autor: David Jérémie Birnbaum, Jocelyne Jacquemier, T Noguchi, Hagay Sobol, José Adélaïde, Fabienne Kerangueven

Publikováno v: Oncology Reports.

Loss of heterozygosity (LOH) at loci from the long arm of chromosome 7 was shown to occur in breast carcinomas. However, the frequency with which this alteration is observed varies from 0 to 40%. We report LOH at three microsatellite markers located

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef55df05bf7c9e4c20dca520bf802e9
https://doi.org/10.3892/or.2.1.89

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ALLELIC LOSS AT CHROMOSOME 8P IN HUMAN BREAST-CANCER

Autor: José Adélaïde, M.-J. Pébusque, Rosette Lidereau, David Jérémie Birnbaum, A Dib, Fabienne Kerangueven, Jocelyne Jacquemier, Michel Longy

Publikováno v: Oncology Reports.

Loss of heterozygosity (LOH) at loci from the short arm of chromosome 8 has been shown to occur in several types of carcinomas. The consensus deletion region has been recently mapped at 8p21-p22, distal to D8S283 and NEFL loci, and proximal to LPL an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57310ed7857fdafc0880d41a2890fadb
https://doi.org/10.3892/or.1.2.393

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