Vidaud D - Search Results

1

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.

2

Structure of the Echinococcus multilocularis U1 snRNA gene repeat.

Bretagne S, Robert B, Vidaud D, Goossens M, Houin R. Bretagne S, et al. Among authors: vidaud d. Mol Biochem Parasitol. 1991 Jun;46(2):285-92. doi: 10.1016/0166-6851(91)90052-8. Mol Biochem Parasitol. 1991. PMID: 1840625

3

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

4

Determination of the spectrum of beta-thalassemia genes in Spain by use of dot-blot analysis of amplified beta-globin DNA.

Amselem S, Nunes V, Vidaud M, Estivill X, Wong C, d'Auriol L, Vidaud D, Galibert F, Baiget M, Goossens M. Amselem S, et al. Among authors: vidaud m, vidaud d, d auriol l. Am J Hum Genet. 1988 Jul;43(1):95-100. Am J Hum Genet. 1988. PMID: 2897787 Free PMC article.

5

A 5' splice-region G----C mutation in exon 1 of the human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia.

Vidaud M, Gattoni R, Stevenin J, Vidaud D, Amselem S, Chibani J, Rosa J, Goossens M. Vidaud M, et al. Among authors: vidaud d. Proc Natl Acad Sci U S A. 1989 Feb;86(3):1041-5. doi: 10.1073/pnas.86.3.1041. Proc Natl Acad Sci U S A. 1989. PMID: 2915972 Free PMC article.

6

Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene.

Vidaud D, Vidaud M, Bahnak BR, Siguret V, Gispert Sanchez S, Laurian Y, Meyer D, Goossens M, Lavergne JM. Vidaud D, et al. Among authors: vidaud m. Eur J Hum Genet. 1993;1(1):30-6. doi: 10.1159/000472385. Eur J Hum Genet. 1993. PMID: 8069649

7

Quantification of apolipoprotein A-I and B messenger RNA in heavy drinkers according to liver disease.

Mathurin P, Vidaud D, Vidaud M, Bedossa P, Paradis V, Ratziu V, Chaput JC, Poynard T. Mathurin P, et al. Among authors: vidaud m, vidaud d. Hepatology. 1996 Jan;23(1):44-51. doi: 10.1002/hep.510230107. Hepatology. 1996. PMID: 8550047

8

Misdiagnosis revealed by genetic linkage analysis in a family with Wilson disease.

Vidaud D, Assouline B, Lecoz P, Cadranel JF, Chappuis P. Vidaud D, et al. Neurology. 1996 May;46(5):1485-6. doi: 10.1212/wnl.46.5.1485. Neurology. 1996. PMID: 8628510 No abstract available.

9

Role of liver extracellular matrix in transcriptional and post-transcriptional regulation of apolipoprotein A-I by hepatocytes.

Paradis V, Laurent A, Mathurin P, Poynard T, Vidaud D, Vidaud M, Bedossa P. Paradis V, et al. Among authors: vidaud m, vidaud d. Cell Mol Biol (Noisy-le-grand). 1996 Jun;42(4):525-34. Cell Mol Biol (Noisy-le-grand). 1996. PMID: 8828908

10

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

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