Peter M - Search Results

1

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: peter m. 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.

2

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: peter m. Cancer Genet Cytogenet. 1990 Mar;45(1):55-62. doi: 10.1016/0165-4608(90)90066-j. Cancer Genet Cytogenet. 1990. PMID: 1967977

3

Sensitive detection of occult Ewing's cells by the reverse transcriptase-polymerase chain reaction.

Peter M, Magdelenat H, Michon J, Melot T, Oberlin O, Zucker JM, Thomas G, Delattre O. Peter M, et al. Br J Cancer. 1995 Jul;72(1):96-100. doi: 10.1038/bjc.1995.283. Br J Cancer. 1995. PMID: 7599072 Free PMC article.

4

An EWS/ERG fusion with a truncated N-terminal domain of EWS in a Ewing's tumor.

Peter M, Mugneret F, Aurias A, Thomas G, Magdelenat H, Delattre O. Peter M, et al. Int J Cancer. 1996 Jul 29;67(3):339-42. doi: 10.1002/(SICI)1097-0215(19960729)67:3<339::AID-IJC6>3.0.CO;2-S. Int J Cancer. 1996. PMID: 8707406

5

Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses.

Mairal A, Pinglier E, Gilbert E, Peter M, Validire P, Desjardins L, Doz F, Aurias A, Couturier J. Mairal A, et al. Among authors: peter m. Genes Chromosomes Cancer. 2000 Aug;28(4):370-9. Genes Chromosomes Cancer. 2000. PMID: 10862045

6

Increased risk of systemic relapses associated with bone marrow micrometastasis and circulating tumor cells in localized ewing tumor.

Schleiermacher G, Peter M, Oberlin O, Philip T, Rubie H, Mechinaud F, Sommelet-Olive D, Landman-Parker J, Bours D, Michon J, Delattre O; Société Française d'Oncologie Pédiatrique. Schleiermacher G, et al. Among authors: peter m. J Clin Oncol. 2003 Jan 1;21(1):85-91. doi: 10.1200/JCO.2003.03.006. J Clin Oncol. 2003. PMID: 12506175

7

High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization.

Fix A, Peter M, Pierron G, Aurias A, Delattre O, Janoueix-Lerosey I. Fix A, et al. Among authors: peter m. Genes Chromosomes Cancer. 2004 Jul;40(3):266-70. doi: 10.1002/gcc.20041. Genes Chromosomes Cancer. 2004. PMID: 15139005

8

Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints.

Zucman J, Delattre O, Desmaze C, Plougastel B, Joubert I, Melot T, Peter M, De Jong P, Rouleau G, Aurias A, et al. Zucman J, et al. Among authors: peter m. Genes Chromosomes Cancer. 1992 Nov;5(4):271-7. doi: 10.1002/gcc.2870050402. Genes Chromosomes Cancer. 1992. PMID: 1283315

9

PCR assay for chromosome 1p deletion in small neuroblastoma samples.

Peter M, Michon J, Vielh P, Neuenschwander S, Nakamura Y, Sonsino E, Zucker JM, Vergnaud G, Thomas G, Delattre O. Peter M, et al. Int J Cancer. 1992 Oct 21;52(4):544-8. doi: 10.1002/ijc.2910520408. Int J Cancer. 1992. PMID: 1399134

10

Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma.

Schleiermacher G, Peter M, Michon J, Hugot JP, Vielh P, Zucker JM, Magdelénat H, Thomas G, Delattre O. Schleiermacher G, et al. Among authors: peter m. Genes Chromosomes Cancer. 1994 Aug;10(4):275-81. doi: 10.1002/gcc.2870100409. Genes Chromosomes Cancer. 1994. PMID: 7522542

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