Lalle P - Search Results

1

Detection of allelic losses on 17q12-q21 chromosomal region in benign lesions and malignant tumors occurring in a familial context.

Lalle P, De Latour M, Rio P, Bignon YJ. Lalle P, et al. Oncogene. 1994 Feb;9(2):437-42. Oncogene. 1994. PMID: 8290255

2

[Hereditary predisposition for cancer of the breast and the ovary].

Lalle P, Stoppa-Lyonnet D, Mazoyer S, Rio P, Girodet C, Hardouin A, Narod SA, Sobol H, Bignon YJ. Lalle P, et al. Bull Cancer. 1993 Oct;80(10):857-65. Bull Cancer. 1993. PMID: 8204923 French.

3

Lack of germ-line mutations in the p53 gene exons 4 to 8 in patients with late-onset second malignant neoplasms.

Lalle P, Moyret C, Bignon YJ. Lalle P, et al. Cancer Genet Cytogenet. 1994 Sep;76(2):148-50. doi: 10.1016/0165-4608(94)90467-7. Cancer Genet Cytogenet. 1994. PMID: 7923066

4

Linkage analysis of 19 French breast cancer families, with five chromosome 17q markers.

Mazoyer S, Lalle P, Narod SA, Bignon YJ, Courjal F, Jamot B, Dutrillaux B, Stoppa-Lyonnett D, Sobol H. Mazoyer S, et al. Among authors: lalle p. Am J Hum Genet. 1993 Apr;52(4):754-60. Am J Hum Genet. 1993. PMID: 8096359 Free PMC article.

5

Screening of inherited breast cancer with DNA markers.

Lalle P, Bignon YJ, Stoppa-Lyonnet D, Narod SA, Mazoyer S, Rio P, Courjal F, Bartholin P, Sobol H. Lalle P, et al. Lancet. 1993 May 29;341(8857):1422. Lancet. 1993. PMID: 8098837 No abstract available.

6

Two germ-line mutations affecting the same nucleotide at codon 257 of p53 gene, a rare site for mutations.

Mazoyer S, Lalle P, Moyret-Lalle C, Marçais C, Schraub S, Frappaz D, Sobol H, Ozturk M. Mazoyer S, et al. Among authors: lalle p. Oncogene. 1994 Apr;9(4):1237-9. Oncogene. 1994. PMID: 8134127

7

Genomic stability and wild-type p53 function of lymphoblastoid cells with germ-line p53 mutation.

Lalle P, Moyret-Lalle C, Wang Q, Vialle JM, Navarro C, Bressac-de Paillerets B, Magaud JP, Ozturk M. Lalle P, et al. Oncogene. 1995 Jun 15;10(12):2447-54. Oncogene. 1995. PMID: 7784096

8

High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium.

Cornelis RS, Neuhausen SL, Johansson O, Arason A, Kelsell D, Ponder BA, Tonin P, Hamann U, Lindblom A, Lalle P, et al. Cornelis RS, et al. Among authors: lalle p. Genes Chromosomes Cancer. 1995 Jul;13(3):203-10. doi: 10.1002/gcc.2870130310. Genes Chromosomes Cancer. 1995. PMID: 7669740

9

Nrh, a human homologue of Nr-13 associates with Bcl-Xs and is an inhibitor of apoptosis.

Aouacheria A, Arnaud E, Venet S, Lalle P, Gouy M, Rigal D, Gillet G. Aouacheria A, et al. Among authors: lalle p. Oncogene. 2001 Sep 13;20(41):5846-55. doi: 10.1038/sj.onc.1204740. Oncogene. 2001. PMID: 11593390

10

Modulation of Nr-13 antideath activity by peptide aptamers.

Nouvion AL, Thibaut J, Lohez OD, Venet S, Colas P, Gillet G, Lalle P. Nouvion AL, et al. Among authors: lalle p. Oncogene. 2007 Feb 1;26(5):701-10. doi: 10.1038/sj.onc.1209832. Epub 2006 Aug 14. Oncogene. 2007. PMID: 16909120

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