Mallet J - Search Results

1

Catecholamine metabolism and psychiatric or behavioral disorders.

Mallet J, Meloni R, Laurent C. Mallet J, et al. Curr Opin Genet Dev. 1994 Jun;4(3):419-26. doi: 10.1016/0959-437x(94)90031-0. Curr Opin Genet Dev. 1994. PMID: 7919920 Review.

2

Catecholamine biosynthetic enzyme expression in neurological and psychiatric disorders.

Meloni R, Dumas S, Mallet J. Meloni R, et al. Among authors: mallet j. Adv Pharmacol. 1998;42:50-3. doi: 10.1016/s1054-3589(08)60693-6. Adv Pharmacol. 1998. PMID: 9327844 No abstract available.

3

Post-genomic era and gene discovery for psychiatric diseases: there is a new art of the trade? The example of the HUMTH01 microsatellite in the Tyrosine Hydroxylase gene.

Meloni R, Biguet NF, Mallet J. Meloni R, et al. Among authors: mallet j. Mol Neurobiol. 2002 Oct-Dec;26(2-3):389-403. doi: 10.1385/MN:26:2-3:389. Mol Neurobiol. 2002. PMID: 12428766 Review.

4

Detection of two new polymorphic sites in the human interleukin-1 beta gene: lack of association with schizophrenia in a French population.

Laurent C, Thibaut F, Ravassard P, Campion D, Samolyk D, Lafargue C, Petit M, Martinez M, Mallet J. Laurent C, et al. Among authors: mallet j. Psychiatr Genet. 1997 Autumn;7(3):103-5. doi: 10.1097/00041444-199723000-00002. Psychiatr Genet. 1997. PMID: 9323321

5

A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro.

Meloni R, Albanèse V, Ravassard P, Treilhou F, Mallet J. Meloni R, et al. Among authors: mallet j. Hum Mol Genet. 1998 Mar;7(3):423-8. doi: 10.1093/hmg/7.3.423. Hum Mol Genet. 1998. PMID: 9466999

6

Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite.

Albanèse V, Biguet NF, Kiefer H, Bayard E, Mallet J, Meloni R. Albanèse V, et al. Among authors: mallet j. Hum Mol Genet. 2001 Aug 15;10(17):1785-92. doi: 10.1093/hmg/10.17.1785. Hum Mol Genet. 2001. PMID: 11532988

7

Association of DNA polymorphism in the first intron of the tyrosine hydroxylase gene with disturbances of the catecholaminergic system in schizophrenia.

Thibaut F, Ribeyre JM, Dourmap N, Meloni R, Laurent C, Campion D, Ménard JF, Dollfus S, Mallet J, Petit M. Thibaut F, et al. Among authors: mallet j. Schizophr Res. 1997 Feb 28;23(3):259-64. doi: 10.1016/s0920-9964(96)00118-1. Schizophr Res. 1997. PMID: 9075305

8

Serotonin transporter gene polymorphism and schizophrenia: an association study.

Bonnet-Brilhault F, Laurent C, Thibaut F, Campion D, Chavand O, Samolyk D, Martinez M, Petit M, Mallet J. Bonnet-Brilhault F, et al. Among authors: mallet j. Biol Psychiatry. 1997 Oct 1;42(7):634-6. doi: 10.1016/S0006-3223(97)00320-X. Biol Psychiatry. 1997. PMID: 9376461 Clinical Trial. No abstract available.

9

Linkage disequilibrium on the COMT gene in French schizophrenics and controls.

de Chaldée M, Laurent C, Thibaut F, Martinez M, Samolyk D, Petit M, Campion D, Mallet J. de Chaldée M, et al. Among authors: mallet j. Am J Med Genet. 1999 Oct 15;88(5):452-7. doi: 10.1002/(sici)1096-8628(19991015)88:5<452::aid-ajmg2>3.3.co;2-s. Am J Med Genet. 1999. PMID: 10490696

10

Paradoxical methylation of the tyrosine hydroxylase gene in mouse preimplantation embryos.

Arányi T, Kerjean A, Tóth S, Mallet J, Meloni R, Páldi A. Arányi T, et al. Among authors: mallet j. Genomics. 2002 Dec;80(6):558-63. doi: 10.1006/geno.2002.7011. Genomics. 2002. PMID: 12504847

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