Vidaud D - Search Results

1

MicroRNAome profiling in benign and malignant neurofibromatosis type 1-associated nerve sheath tumors: evidences of PTEN pathway alterations in early NF1 tumorigenesis.

Masliah-Planchon J, Pasmant E, Luscan A, Laurendeau I, Ortonne N, Hivelin M, Varin J, Valeyrie-Allanore L, Dumaine V, Lantieri L, Leroy K, Parfait B, Wolkenstein P, Vidaud M, Vidaud D, Bièche I. Masliah-Planchon J, et al. Among authors: vidaud m, vidaud d. BMC Genomics. 2013 Jul 13;14:473. doi: 10.1186/1471-2164-14-473. BMC Genomics. 2013. PMID: 23848554 Free PMC article.

2

Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior.

Attree O, Vidaud D, Vidaud M, Amselem S, Lavergne JM, Goossens M. Attree O, et al. Among authors: vidaud m, vidaud d. Genomics. 1989 Apr;4(3):266-72. doi: 10.1016/0888-7543(89)90330-3. Genomics. 1989. PMID: 2714791

3

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.

4

[Exclusive nodular plexiform neurofibroma. An unusual case of neurofibromatosis type 1].

Benchikhi H, Zeller J, Wolkenstein P, Wechsler J, Vidaud D, Revuz J. Benchikhi H, et al. Among authors: vidaud d. Ann Dermatol Venereol. 1995;122(9):601-3. Ann Dermatol Venereol. 1995. PMID: 8745684 French.

5

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

6

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

7

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

8

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

9

Quantitation of MYC gene expression in sporadic breast tumors with a real-time reverse transcription-PCR assay.

Bièche I, Laurendeau I, Tozlu S, Olivi M, Vidaud D, Lidereau R, Vidaud M. Bièche I, et al. Among authors: vidaud m, vidaud d. Cancer Res. 1999 Jun 15;59(12):2759-65. Cancer Res. 1999. PMID: 10383126

10

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

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