Hudson TJ - Search Results

1

Susceptibility to leprosy is associated with PARK2 and PACRG.

Mira MT, Alcaïs A, Nguyen VT, Moraes MO, Di Flumeri C, Vu HT, Mai CP, Nguyen TH, Nguyen NB, Pham XK, Sarno EN, Alter A, Montpetit A, Moraes ME, Moraes JR, Doré C, Gallant CJ, Lepage P, Verner A, Van De Vosse E, Hudson TJ, Abel L, Schurr E. Mira MT, et al. Among authors: hudson tj. Nature. 2004 Feb 12;427(6975):636-40. doi: 10.1038/nature02326. Epub 2004 Jan 25. Nature. 2004. PMID: 14737177 Free article.

2

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.

Engert JC, Doré C, Mercier J, Ge B, Bétard C, Rioux JD, Owen C, Bérubé P, Devon K, Birren B, Melançon SB, Morgan K, Hudson TJ, Richter A. Engert JC, et al. Among authors: hudson tj. Genomics. 1999 Dec 1;62(2):156-64. doi: 10.1006/geno.1999.6003. Genomics. 1999. PMID: 10610707

3

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.

Engert JC, Bérubé P, Mercier J, Doré C, Lepage P, Ge B, Bouchard JP, Mathieu J, Melançon SB, Schalling M, Lander ES, Morgan K, Hudson TJ, Richter A. Engert JC, et al. Among authors: hudson tj. Nat Genet. 2000 Feb;24(2):120-5. doi: 10.1038/72769. Nat Genet. 2000. PMID: 10655055

4

Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA. Bétard C, et al. Among authors: hudson tj. Am J Hum Genet. 2000 Jul;67(1):222-8. doi: 10.1086/302993. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820129 Free PMC article.

5

Molecular scanning of the human PPARa gene: association of the L162v mutation with hyperapobetalipoproteinemia.

Vohl MC, Lepage P, Gaudet D, Brewer CG, Bétard C, Perron P, Houde G, Cellier C, Faith JM, Després JP, Morgan K, Hudson TJ. Vohl MC, et al. Among authors: hudson tj. J Lipid Res. 2000 Jun;41(6):945-52. J Lipid Res. 2000. PMID: 10828087 Free article.

6

Complete nucleotide sequence and genomic structure of the human NRAMP1 gene region on chromosome region 2q35.

Marquet S, Lepage P, Hudson TJ, Musser JM, Schurr E. Marquet S, et al. Among authors: hudson tj. Mamm Genome. 2000 Sep;11(9):755-62. doi: 10.1007/s003350010151. Mamm Genome. 2000. PMID: 10967134

7

A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.

Seyda A, Newbold RF, Hudson TJ, Verner A, MacKay N, Winter S, Feigenbaum A, Malaney S, Gonzalez-Halphen D, Cuthbert AP, Robinson BH. Seyda A, et al. Among authors: hudson tj. Am J Hum Genet. 2001 Feb;68(2):386-96. doi: 10.1086/318196. Epub 2001 Jan 10. Am J Hum Genet. 2001. PMID: 11156534 Free PMC article.

8

A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.

Héon E, Paterson AD, Fraser M, Billingsley G, Priston M, Balmer A, Schorderet DF, Verner A, Hudson TJ, Munier FL. Héon E, et al. Among authors: hudson tj. Am J Hum Genet. 2001 Mar;68(3):772-7. doi: 10.1086/318798. Epub 2001 Feb 5. Am J Hum Genet. 2001. PMID: 11179024 Free PMC article.

9

A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.

Laitinen T, Daly MJ, Rioux JD, Kauppi P, Laprise C, Petäys T, Green T, Cargill M, Haahtela T, Lander ES, Laitinen LA, Hudson TJ, Kere J. Laitinen T, et al. Among authors: hudson tj. Nat Genet. 2001 May;28(1):87-91. doi: 10.1038/ng0501-87. Nat Genet. 2001. PMID: 11326283

10

A distal upstream enhancer from the myelin basic protein gene regulates expression in myelin-forming schwann cells.

Forghani R, Garofalo L, Foran DR, Farhadi HF, Lepage P, Hudson TJ, Tretjakoff I, Valera P, Peterson A. Forghani R, et al. Among authors: hudson tj. J Neurosci. 2001 Jun 1;21(11):3780-7. doi: 10.1523/JNEUROSCI.21-11-03780.2001. J Neurosci. 2001. PMID: 11356866 Free PMC article.

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