Nagatsu T - Search Results

1

DRD2 allele frequencies and linkage disequilibria, including the -141CIns/Del promoter polymorphism, in European-American, African-American, and Japanese subjects.

Gelernter J, Kranzler H, Cubells JF, Ichinose H, Nagatsu T. Gelernter J, et al. Among authors: nagatsu t. Genomics. 1998 Jul 1;51(1):21-6. doi: 10.1006/geno.1998.5264. Genomics. 1998. PMID: 9693029 Free article.

2

Population genetics of a functional variant of the dopamine beta-hydroxylase gene (DBH).

Cubells JF, Kobayashi K, Nagatsu T, Kidd KK, Kidd JR, Calafell F, Kranzler HR, Ichinose H, Gelernter J. Cubells JF, et al. Among authors: nagatsu t. Am J Med Genet. 1997 Jul 25;74(4):374-9. doi: 10.1002/(sici)1096-8628(19970725)74:4<374::aid-ajmg7>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9259372

3

Dopamine beta-hydroxylase: two polymorphisms in linkage disequilibrium at the structural gene DBH associate with biochemical phenotypic variation.

Cubells JF, van Kammen DP, Kelley ME, Anderson GM, O'Connor DT, Price LH, Malison R, Rao PA, Kobayashi K, Nagatsu T, Gelernter J. Cubells JF, et al. Among authors: nagatsu t. Hum Genet. 1998 May;102(5):533-40. doi: 10.1007/s004390050736. Hum Genet. 1998. PMID: 9654201

4

A quantitative-trait analysis of human plasma-dopamine beta-hydroxylase activity: evidence for a major functional polymorphism at the DBH locus.

Zabetian CP, Anderson GM, Buxbaum SG, Elston RC, Ichinose H, Nagatsu T, Kim KS, Kim CH, Malison RT, Gelernter J, Cubells JF. Zabetian CP, et al. Among authors: nagatsu t. Am J Hum Genet. 2001 Feb;68(2):515-22. doi: 10.1086/318198. Epub 2001 Jan 19. Am J Hum Genet. 2001. PMID: 11170900 Free PMC article.

5

[Molecular biology of hereditary dystonia].

Nagatsu T, Ichinose H. Nagatsu T, et al. No To Hattatsu. 1998 Mar;30(2):93-100. No To Hattatsu. 1998. PMID: 9545771 Review. Japanese.

6

[Molecular genetics of aromatic L-amino acid decarboxylase].

Ichinose H, Nagatsu T. Ichinose H, et al. Among authors: nagatsu t. Yakubutsu Seishin Kodo. 1993 Aug;13(4):251-6. Yakubutsu Seishin Kodo. 1993. PMID: 8237142 Review. Japanese.

7

Molecular genetics of hereditary dystonia--mutations in the GTP cyclohydrolase I gene.

Ichinose H, Nagatsu T. Ichinose H, et al. Among authors: nagatsu t. Brain Res Bull. 1997;43(1):35-8. doi: 10.1016/s0361-9230(96)00353-x. Brain Res Bull. 1997. PMID: 9205791 Review.

8

[Autosomal-dominant DOPA-responsive dystonia, caused by mutations in the GTP-cyclohydrolase I gene].

Nagatsu T, Ichinose H. Nagatsu T, et al. Vopr Med Khim. 1998 May-Jun;44(3):225-8. Vopr Med Khim. 1998. PMID: 9703621 Russian.

9

[Molecular genetics of hereditary progressive dystonia (HPD/Segawa's disease)].

Ichinose H, Nagatsu T. Ichinose H, et al. Among authors: nagatsu t. Nihon Rinsho. 1996 May;54(5):1453-9. Nihon Rinsho. 1996. PMID: 8965384 Review. Japanese.

10

GTP cyclohydrolase I gene, dystonia, juvenile parkinsonism, and Parkinson's disease.

Nagatsu T, Ichinose H. Nagatsu T, et al. J Neural Transm Suppl. 1997;49:203-9. J Neural Transm Suppl. 1997. PMID: 9266429 Review.

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