Aurias A - Search Results

1

Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses.

Couturier J, Delattre O, Kujas M, Philippon J, Peter M, Rouleau G, Aurias A, Thomas G. Couturier J, et al. Among authors: aurias a. Cancer Genet Cytogenet. 1990 Mar;45(1):55-62. doi: 10.1016/0165-4608(90)90066-j. Cancer Genet Cytogenet. 1990. PMID: 1967977

2

Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridization.

Delattre O, Grunwald M, Bernard A, Grunwald D, Thomas G, Frelat G, Aurias A. Delattre O, et al. Among authors: aurias a. Hum Genet. 1988 Feb;78(2):140-3. doi: 10.1007/BF00278184. Hum Genet. 1988. PMID: 3123358

3

Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors.

Desmaze C, Brizard F, Turc-Carel C, Melot T, Delattre O, Thomas G, Aurias A. Desmaze C, et al. Among authors: aurias a. Cancer Genet Cytogenet. 1997 Aug;97(1):12-9. doi: 10.1016/s0165-4608(96)00326-3. Cancer Genet Cytogenet. 1997. PMID: 9242212

4

hSNF5/INI1 inactivation is mainly associated with homozygous deletions and mitotic recombinations in rhabdoid tumors.

Rousseau-Merck MF, Versteege I, Legrand I, Couturier J, Mairal A, Delattre O, Aurias A. Rousseau-Merck MF, et al. Among authors: aurias a. Cancer Res. 1999 Jul 1;59(13):3152-6. Cancer Res. 1999. PMID: 10397258

5

CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases.

Brisset S, Schleiermacher G, Peter M, Mairal A, Oberlin O, Delattre O, Aurias A. Brisset S, et al. Among authors: aurias a. Cancer Genet Cytogenet. 2001 Oct 1;130(1):57-61. doi: 10.1016/s0165-4608(01)00454-x. Cancer Genet Cytogenet. 2001. PMID: 11672775 Review.

6

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma.

Schleiermacher G, Janoueix-Lerosey I, Combaret V, Derré J, Couturier J, Aurias A, Delattre O. Schleiermacher G, et al. Among authors: aurias a. Cancer Genet Cytogenet. 2003 Feb;141(1):32-42. doi: 10.1016/s0165-4608(02)00644-1. Cancer Genet Cytogenet. 2003. PMID: 12581896

7

Variety and complexity of chromosome 17 translocations in neuroblastoma.

Schleiermacher G, Raynal V, Janoueix-Lerosey I, Combaret V, Aurias A, Delattre O. Schleiermacher G, et al. Among authors: aurias a. Genes Chromosomes Cancer. 2004 Feb;39(2):143-50. doi: 10.1002/gcc.10313. Genes Chromosomes Cancer. 2004. PMID: 14695994

8

Chromosome mechanisms and INI1 inactivation in human and mouse rhabdoid tumors.

Rousseau-Merck MF, Fiette L, Klochendler-Yeivin A, Delattre O, Aurias A. Rousseau-Merck MF, et al. Among authors: aurias a. Cancer Genet Cytogenet. 2005 Mar;157(2):127-33. doi: 10.1016/j.cancergencyto.2004.06.006. Cancer Genet Cytogenet. 2005. PMID: 15721633

9

Mapping of human chromosome 22 with a panel of somatic cell hybrids.

Delattre O, Azambuja CJ, Aurias A, Zucman J, Peter M, Zhang F, Hors-Cayla MC, Rouleau G, Thomas G. Delattre O, et al. Among authors: aurias a. Genomics. 1991 Apr;9(4):721-7. doi: 10.1016/0888-7543(91)90366-m. Genomics. 1991. PMID: 2037296

10

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.

Zhang FR, Delattre O, Rouleau G, Couturier J, Lefrançois, Thomas G, Aurias A. Zhang FR, et al. Among authors: aurias a. Genomics. 1990 Jan;6(1):174-7. doi: 10.1016/0888-7543(90)90463-5. Genomics. 1990. PMID: 2303258

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