Chaffanet M - Search Results

1

Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.

Popovici C, Basset C, Bertucci F, Orsetti B, Adélaide J, Mozziconacci MJ, Conte N, Murati A, Ginestier C, Charafe-Jauffret E, Ethier SP, Lafage-Pochitaloff M, Theillet C, Birnbaum D, Chaffanet M. Popovici C, et al. Among authors: chaffanet m. Genes Chromosomes Cancer. 2002 Nov;35(3):204-18. doi: 10.1002/gcc.10107. Genes Chromosomes Cancer. 2002. PMID: 12353263

2

Characterization of the region of the short arm of chromosome 8 amplified in breast carcinoma.

Dib A, Adélaïde J, Chaffanet M, Imbert A, Le Paslier D, Jacquemier J, Gaudray P, Theillet C, Birnbaum D, Pébusque MJ. Dib A, et al. Among authors: chaffanet m. Oncogene. 1995 Mar 2;10(5):995-1001. Oncogene. 1995. PMID: 7898940

3

A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8.

Chaffanet M, Imbert A, Adélaïde J, Le Paslier D, Wagner MJ, Wells DE, Birnbaum D, Pébusque MJ. Chaffanet M, et al. Cytogenet Cell Genet. 1996;72(1):63-8. doi: 10.1159/000134164. Cytogenet Cell Genet. 1996. PMID: 8565638

4

Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia.

Soenen V, Chaffanet M, Preudhomme C, Dib A, Lai JL, Fletcher JA, Birnbaurn D, Pébusque MJ. Soenen V, et al. Among authors: chaffanet m. Genes Chromosomes Cancer. 1996 Mar;15(3):191-4. doi: 10.1002/(SICI)1098-2264(199603)15:3<191::AID-GCC9>3.0.CO;2-Y. Genes Chromosomes Cancer. 1996. PMID: 8721686

5

Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome.

Imbert A, Chaffanet M, Essioux L, Noguchi T, Adélaïde J, Kerangueven F, Le Paslier D, Bonaïti-Pellié C, Sobol H, Birnbaum D, Pébusque MJ. Imbert A, et al. Among authors: chaffanet m. Genomics. 1996 Feb 15;32(1):29-38. doi: 10.1006/geno.1996.0073. Genomics. 1996. PMID: 8786118

6

Regional assignment of 64 human gene transcripts on chromosome 8.

Ugolini F, Chaffanet M, Houlgatte R, Patterson D, Wells D, Auffray C, Birnbaum D, Pébusque MJ. Ugolini F, et al. Among authors: chaffanet m. Cytogenet Cell Genet. 1997;77(3-4):197-200. doi: 10.1159/000134575. Cytogenet Cell Genet. 1997. PMID: 9284915

7

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12.

Chaffanet M, Popovici C, Leroux D, Jacrot M, Adélaïde J, Dastugue N, Grégoire MJ, Hagemeijer A, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ. Chaffanet M, et al. Oncogene. 1998 Feb 19;16(7):945-9. doi: 10.1038/sj.onc.1201601. Oncogene. 1998. PMID: 9484786

8

Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13).

Popovici C, Adélaïde J, Ollendorff V, Chaffanet M, Guasch G, Jacrot M, Leroux D, Birnbaum D, Pébusque MJ. Popovici C, et al. Among authors: chaffanet m. Proc Natl Acad Sci U S A. 1998 May 12;95(10):5712-7. doi: 10.1073/pnas.95.10.5712. Proc Natl Acad Sci U S A. 1998. PMID: 9576949 Free PMC article.

9

Chromosome region 8p11-p21: refined mapping and molecular alterations in breast cancer.

Adélaïde J, Chaffanet M, Imbert A, Allione F, Geneix J, Popovici C, van Alewijk D, Trapman J, Zeillinger R, Børresen-Dale AL, Lidereau R, Birnbaum D, Pébusque MJ. Adélaïde J, et al. Among authors: chaffanet m. Genes Chromosomes Cancer. 1998 Jul;22(3):186-99. doi: 10.1002/(sici)1098-2264(199807)22:3<186::aid-gcc4>3.0.co;2-s. Genes Chromosomes Cancer. 1998. PMID: 9624530

10

A case of inv(8)(p11q24) associated with acute myeloid leukemia involves the MOZ and CBP genes in a masked t(8;16).

Chaffanet M, Mozziconacci MJ, Fernandez F, Sainty D, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ. Chaffanet M, et al. Genes Chromosomes Cancer. 1999 Oct;26(2):161-5. Genes Chromosomes Cancer. 1999. PMID: 10469454

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