David V - Search Results

1

Pharmacogenetic-Whole blood and intracellular pharmacokinetic-Pharmacodynamic (PG-PK2-PD) relationship of tacrolimus in liver transplant recipients.

Tron C, Woillard JB, Houssel-Debry P, David V, Jezequel C, Rayar M, Balakirouchenane D, Blanchet B, Debord J, Petitcollin A, Roussel M, Verdier MC, Bellissant E, Lemaitre F. Tron C, et al. Among authors: david v. PLoS One. 2020 Mar 12;15(3):e0230195. doi: 10.1371/journal.pone.0230195. eCollection 2020. PLoS One. 2020. PMID: 32163483 Free PMC article.

2

PharmFrag: An Easy and Fast Multiplex Pharmacogenetics Assay to Simultaneously Analyze 9 Genetic Polymorphisms Involved in Response Variability of Anticancer Drugs.

Bouvet R, Verdier MC, El Baroudi Y, Galibert MD, David V, Schutz S, Tron C. Bouvet R, et al. Among authors: david v. Int J Mol Sci. 2020 Dec 17;21(24):9650. doi: 10.3390/ijms21249650. Int J Mol Sci. 2020. PMID: 33348915 Free PMC article.

3

Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein.

Kim A, Le Douce J, Diab F, Ferovova M, Dubourg C, Odent S, Dupé V, David V, Diambra L, Watrin E, de Tayrac M. Kim A, et al. Among authors: david v. Brain. 2020 Jul 1;143(7):2027-2038. doi: 10.1093/brain/awaa152. Brain. 2020. PMID: 32542401

4

Phenotypic expression in detected C282Y homozygous women depends on body mass index.

Lainé F, Jouannolle AM, Morcet J, Brigand A, Pouchard M, Lafraise B, Mosser J, David V, Deugnier Y. Lainé F, et al. Among authors: david v. J Hepatol. 2005 Dec;43(6):1055-9. doi: 10.1016/j.jhep.2005.05.027. Epub 2005 Jun 28. J Hepatol. 2005. PMID: 16139917

5

Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.

Détivaud L, Island ML, Jouanolle AM, Ropert M, Bardou-Jacquet E, Le Lan C, Mosser A, Leroyer P, Deugnier Y, David V, Brissot P, Loréal O. Détivaud L, et al. Among authors: david v. Hum Mutat. 2013 Nov;34(11):1529-36. doi: 10.1002/humu.22396. Epub 2013 Sep 11. Hum Mutat. 2013. PMID: 23943237

6

Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations.

Aguilella C, Dubourg C, Attia-Sobol J, Vigneron J, Blayau M, Pasquier L, Lazaro L, Odent S, David V. Aguilella C, et al. Among authors: david v. Hum Genet. 2003 Feb;112(2):131-4. doi: 10.1007/s00439-002-0862-8. Epub 2002 Nov 21. Hum Genet. 2003. PMID: 12522553

7

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.

Dubourg C, Lazaro L, Pasquier L, Bendavid C, Blayau M, Le Duff F, Durou MR, Odent S, David V. Dubourg C, et al. Among authors: david v. Hum Mutat. 2004 Jul;24(1):43-51. doi: 10.1002/humu.20056. Hum Mutat. 2004. PMID: 15221788

8

Phenotypic and molecular variability of the holoprosencephalic spectrum.

Lazaro L, Dubourg C, Pasquier L, Le Duff F, Blayau M, Durou MR, de la Pintière AT, Aguilella C, David V, Odent S. Lazaro L, et al. Among authors: david v. Am J Med Genet A. 2004 Aug 15;129A(1):21-4. doi: 10.1002/ajmg.a.30110. Am J Med Genet A. 2004. PMID: 15266610

9

Functional characterization of sonic hedgehog mutations associated with holoprosencephaly.

Traiffort E, Dubourg C, Faure H, Rognan D, Odent S, Durou MR, David V, Ruat M. Traiffort E, et al. Among authors: david v. J Biol Chem. 2004 Oct 8;279(41):42889-97. doi: 10.1074/jbc.M405161200. Epub 2004 Jul 28. J Biol Chem. 2004. PMID: 15292211 Free article.

10

Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes.

Bendavid C, Dubourg C, Gicquel I, Pasquier L, Saugier-Veber P, Durou MR, Jaillard S, Frébourg T, Haddad BR, Henry C, Odent S, David V. Bendavid C, et al. Among authors: david v. Hum Genet. 2006 Mar;119(1-2):1-8. doi: 10.1007/s00439-005-0097-6. Epub 2005 Dec 2. Hum Genet. 2006. PMID: 16323008

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