J. Grosgeorge

发表

É. Khandjian, E. Bechara, L. Davidovic, 2006, Nucleic acids research.

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.

Cloning, chromosal mapping, and tissue expression of the gene encoding the human Eph-family kinase ligand ephrin-A2.

J. Grosgeorge, H. Aasheim, T. Logtenberg, 1998, Biochemical and biophysical research communications.

Novel mutations in the TCIRG1 gene encoding the a3 subunit of the vacuolar proton pump in patients affected by infantile malignant osteopetrosis

A. Fischer, N. Philip, J. Grosgeorge, 2003, Human mutation.

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

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

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia.

P. Marynen, Caiying Guo, H. Cavé, 1996, Blood.

Deregulation of the platelet-derived growth factor β-chain gene via fusion with collagen gene COL1A1 in dermatof ibrosarcoma protuberans and giant-cell fibroblastoma

J. Dumanski, J. Coindre, J. Grosgeorge, 1997, Nature Genetics.

Structural analysis, expression, and chromosomal localization of the mouse ikba gene

J. Grosgeorge, R. Schmid, A. Livolsi, 1999, Immunogenetics.

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

J. Grosgeorge, C. Turc‐Carel, G. Lenaers, 2000, Nature Genetics.

Localization of 11q13 loci with respect to regional chromosomal breakpoints.

D. Birnbaum, G. Evans, K. Huebner, 1992, Genomics.

Distinct MDM2 and P14ARF expression and centrosome amplification in well‐differentiated liposarcomas

J. Grosgeorge, C. Turc‐Carel, S. Marcié, 2004, Genes, chromosomes & cancer.

Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia.

P. Marynen, J. Grosgeorge, J. Cools, 1997, Blood.

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes.

P. Marynen, J. Grosgeorge, S. Raynaud, 1996, Blood.

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

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

Comparative genomic hybridization reveals novel chromosome deletions in 90 primary soft tissue tumors.

P. Terrier, J. Coindre, J. Grosgeorge, 1999, Cancer genetics and cytogenetics.

Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinoma.

D. Birnbaum, J. Grosgeorge, C. Theillet, 1997, Cytogenetics and cell genetics.

The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants.

O. Jaillon, J. Grosgeorge, G. Carle, 2000, Bone.

myelodysplastic syndromes in recurring chromosomal abnormality involving the TEL gene (ETV6) Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a

P. Marynen, J. Grosgeorge, N. Ayraud, 2011 .

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

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

Expanded range of 11q13 breakpoints with differing patterns of cyclin D1 expression in B‐cell malignancies

B. Klein, J. Grosgeorge, C. Bastard, 1993, Genes, chromosomes & cancer.

A 5.5-Mb high-resolution integrated map of distal 11q13.

D. Le Paslier, N. Nowak, T. Shows, 1997, Genomics.

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

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

Human gp130 transducer chain gene (IL6ST) is localized to chromosome band 5q11 and possesses a pseudogene on chromosome band 17p11.

J. Grosgeorge, C. Theillet, C. Rodríguez, 1995, Cytogenetics and cell genetics.

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.

Comparative genomic hybridization reveals novel chromosome deletions in 90 primary soft tissue tumors.

P. Terrier, J. Coindre, J. Grosgeorge, 1999, Cancer genetics and cytogenetics.

The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism.

M. Lazdunski, J. Grosgeorge, J. Hugnot, 1997, Genomics.