A. Courseaux

发表

Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation.

Patrick Gaudray, A. Viale, B. Dutrillaux, 2003, Genome research.

Amplification of 11q13 DNA sequences in human breast cancer: D11S97 identifies a region tightly linked to BCL1 which can be amplified separately.

C. Theillet, G. Carle, P. Szepetowski, 1992, Oncogene.

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.

W. V. D. Van de Ven, R. Thakker, G. Carle, 1997, Genomics.

Framework YAC contig anchored into a 3.2-Mb high-resolution physical map in proximal 11q13.

J. Todd, N. Nowak, T. Shows, 1997, Genomics.

Fine mapping of the MLK-3 gene within 11q13 and its exclusion as the MEN1 susceptibility gene

C. Larsson, B. Teh, N. Lassam, 1997, Human Genetics.

Structural and Content Diversity of Mitochondrial Genome in Beet: A Comparative Genomic Analysis

V. Barbe, B. Vacherie, P. Lenoble, 2011, Genome biology and evolution.

Birth of Two Chimeric Genes in the Hominidae Lineage

J. Nahon, A. Courseaux, 2001, Science.

Cloning of hOST-PTP: the only example of a protein-tyrosine-phosphatase the function of which has been lost between rodent and human.

C. Dani, P. Peraldi, A. Courseaux, 2004, Biochemical and biophysical research communications.

DNA amplification at 11q13.5-q14 in human breast cancer.

D. Birnbaum, J. Grosgeorge, C. Theillet, 1992, Oncogene.

Rearrangement of proximal 11q13 band in a CMML in acute transformation.

C. Larsson, J. Grosgeorge, N. Ayraud, 1995, Leukemia.

Structure and expression of the variant melanin-concentrating hormone genes: only PMCHL1 is transcribed in the developing human brain and encodes a putative protein.

A. Viale, D. Jordan, C. Breton, 2000, Molecular biology and evolution.

Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3.

F. Hecht, J. Grosgeorge, B. Hecht, 1997, Cytogenetics and cell genetics.

Genetic testing in presymptomatic diagnosis of multiple endocrine neoplasia.

I. Schuffenecker, A. Calender, S. Giraud, 1997, Hormone Research.

Human EMK1 is located on 11q12-q13, close to COX8 and FTH1

J. Grosgeorge, J. Inglis, A. Courseaux, 1995, Mammalian Genome.

Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).

C. Larsson, B. Teh, S. Forbes, 1996, Genomics.

Determination of retinoid activity by an enzyme-linked immunosorbent assay.

B. Shroot, U. Reichert, A. Courseaux, 1991, Analytical biochemistry.

Coamplification in human breast-tumors and physical linkage at chromosomal band 12p13, of ccnd2 and fgf6 genes.

D. Birnbaum, C. Theillet, M. Pébusque, 1994, International journal of oncology.