Vidaud M - Search Results

1

Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness.

Bahuau M, Vidaud D, Kujas M, Palangié A, Assouline B, Chaignaud-Lebreton M, Prieur M, Vidaud M, Harpey JP, Lafourcade J, Caille B. Bahuau M, et al. Among authors: vidaud m, vidaud d. Ann Genet. 1997;40(2):78-91. Ann Genet. 1997. PMID: 9259954

2

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.

Bahuau M, Vidaud D, Jenkins RB, Bièche I, Kimmel DW, Assouline B, Smith JS, Alderete B, Cayuela JM, Harpey JP, Caille B, Vidaud M. Bahuau M, et al. Among authors: vidaud m, vidaud d. Cancer Res. 1998 Jun 1;58(11):2298-303. Cancer Res. 1998. PMID: 9622062

3

Myotonic dystrophy protein kinase gene expression in skeletal muscle from congenitally affected infants.

Laurent A, Costa JM, Assouline B, Voyer M, Vidaud M. Laurent A, et al. Among authors: vidaud m. Ann Genet. 1997;40(3):169-74. Ann Genet. 1997. PMID: 9401107

4

Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome.

Bahuau M, Houdayer C, Assouline B, Blanchet-Bardon C, Le Merrer M, Lyonnet S, Giraud S, Récan D, Lakhdar H, Vidaud M, Vidaud D. Bahuau M, et al. Among authors: vidaud m, vidaud d. Am J Med Genet. 1998 Jan 23;75(3):265-72. Am J Med Genet. 1998. PMID: 9475595

5

TaqMan PCR-based gene dosage assay for predictive testing in individuals from a cancer family with INK4 locus haploinsufficiency.

Laurendeau I, Bahuau M, Vodovar N, Larramendy C, Olivi M, Bieche I, Vidaud M, Vidaud D. Laurendeau I, et al. Among authors: vidaud m, vidaud d. Clin Chem. 1999 Jul;45(7):982-6. Clin Chem. 1999. PMID: 10388473

6

Human TIP49b/RUVBL2 gene: genomic structure, expression pattern, physical link to the human CGB/LHB gene cluster on chromosome 19q13.3.

Parfait B, Giovangrandi Y, Asheuer M, Laurendeau I, Olivi M, Vodovar N, Vidaud D, Vidaud M, Bièche I. Parfait B, et al. Among authors: vidaud m, vidaud d. Ann Genet. 2000 Apr-Jun;43(2):69-74. doi: 10.1016/s0003-3995(00)01016-9. Ann Genet. 2000. PMID: 10998447

7

Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genes.

Bretagne S, Assouline B, Vidaud D, Houin R, Vidaud M. Bretagne S, et al. Among authors: vidaud m, vidaud d. Exp Parasitol. 1996 Apr;82(3):324-8. doi: 10.1006/expr.1996.0040. Exp Parasitol. 1996. PMID: 8631384 No abstract available.

8

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.

Bahuau M, Flintoff W, Assouline B, Lyonnet S, Le Merrer M, Prieur M, Guilloud-Bataille M, Feingold N, Munnich A, Vidaud M, Vidaud D. Bahuau M, et al. Among authors: vidaud m, vidaud d. Am J Med Genet. 1996 Dec 18;66(3):347-55. doi: 10.1002/(SICI)1096-8628(19961218)66:3<347::AID-AJMG20>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8985499

9

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

Pasmant E, Laurendeau I, Héron D, Vidaud M, Vidaud D, Bièche I. Pasmant E, et al. Among authors: vidaud m, vidaud d. Cancer Res. 2007 Apr 15;67(8):3963-9. doi: 10.1158/0008-5472.CAN-06-2004. Cancer Res. 2007. PMID: 17440112

10

Novel approach to quantitative polymerase chain reaction using real-time detection: application to the detection of gene amplification in breast cancer.

Bièche I, Olivi M, Champème MH, Vidaud D, Lidereau R, Vidaud M. Bièche I, et al. Among authors: vidaud m, vidaud d. Int J Cancer. 1998 Nov 23;78(5):661-6. doi: 10.1002/(sici)1097-0215(19981123)78:5<661::aid-ijc22>3.0.co;2-i. Int J Cancer. 1998. PMID: 9808539

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