Delattre O - Search Results

1

The neurofibromatosis type 2 gene is inactivated in schwannomas.

Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA. Twist EC, et al. Among authors: delattre o. Hum Mol Genet. 1994 Jan;3(1):147-51. doi: 10.1093/hmg/3.1.147. Hum Mol Genet. 1994. PMID: 8162016

2

Allelic loss on chromosome 22 correlates with histopathological predictors of recurrence of meningiomas.

Sanson M, Richard S, Delattre O, Poliwka M, Mikol J, Philippon J, Thomas G. Sanson M, et al. Among authors: delattre o. Int J Cancer. 1992 Feb 1;50(3):391-4. doi: 10.1002/ijc.2910500311. Int J Cancer. 1992. PMID: 1346529

3

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. Among authors: delattre o. Int J Cancer. 1992 Oct 21;52(4):544-8. doi: 10.1002/ijc.2910520408. Int J Cancer. 1992. PMID: 1399134

4

Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours.

Delattre O, Zucman J, Plougastel B, Desmaze C, Melot T, Peter M, Kovar H, Joubert I, de Jong P, Rouleau G, et al. Delattre O, et al. Nature. 1992 Sep 10;359(6391):162-5. doi: 10.1038/359162a0. Nature. 1992. PMID: 1522903

5

In situ hybridization of PCR amplified inter-Alu sequences from a hybrid cell line.

Desmaze C, Zucman J, Delattre O, Thomas G, Aurias A. Desmaze C, et al. Among authors: delattre o. Hum Genet. 1992 Mar;88(5):541-4. doi: 10.1007/BF00219341. Hum Genet. 1992. PMID: 1551656

6

Rapid isolation of cosmids from defined subregions by differential Alu-PCR hybridization on chromosome 22-specific library.

Zucman J, Delattre O, Desmaze C, Azambuja C, Rouleau G, De Jong P, Aurias A, Thomas G. Zucman J, et al. Among authors: delattre o. Genomics. 1992 Jun;13(2):395-401. doi: 10.1016/0888-7543(92)90259-u. Genomics. 1992. PMID: 1612598

7

Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2).

Aubry M, Marineau C, Zhang FR, Zahed L, Figlewicz D, Delattre O, Thomas G, de Jong PJ, Julien JP, Rouleau GA. Aubry M, et al. Among authors: delattre o. Genomics. 1992 Jul;13(3):641-8. doi: 10.1016/0888-7543(92)90135-f. Genomics. 1992. PMID: 1639391

8

Association of Ki-ras mutation with differentiation and tumor-formation pathways in colorectal carcinoma.

Laurent-Puig P, Olschwang S, Delattre O, Validire P, Melot T, Mosseri V, Salmon RJ, Thomas G. Laurent-Puig P, et al. Among authors: delattre o. Int J Cancer. 1991 Sep 9;49(2):220-3. doi: 10.1002/ijc.2910490213. Int J Cancer. 1991. PMID: 1652568

9

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas.

Fontaine B, Sanson M, Delattre O, Menon AG, Rouleau GA, Seizinger BR, Jewell AF, Hanson MP, Aurias A, Martuza RL, et al. Fontaine B, et al. Among authors: delattre o. Genomics. 1991 May;10(1):280-3. doi: 10.1016/0888-7543(91)90513-e. Genomics. 1991. PMID: 1675196

10

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

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