Ichinose H - Search Results

1

GTP cyclohydrolase I gene in hereditary progressive dystonia with marked diurnal fluctuation.

Ichinose H, Ohye T, Segawa M, Nomura Y, Endo K, Tanaka H, Tsuji S, Fujita K, Nagatsu T. Ichinose H, et al. Neurosci Lett. 1995 Aug 18;196(1-2):5-8. doi: 10.1016/0304-3940(95)11820-m. Neurosci Lett. 1995. PMID: 7501255

2

Multiple mRNA forms of human GTP cyclohydrolase I.

Togari A, Ichinose H, Matsumoto S, Fujita K, Nagatsu T. Togari A, et al. Among authors: ichinose h. Biochem Biophys Res Commun. 1992 Aug 31;187(1):359-65. doi: 10.1016/s0006-291x(05)81501-3. Biochem Biophys Res Commun. 1992. PMID: 1520321

3

GTP cyclohydrolase I activity in mononuclear blood cells in juvenile parkinsonism.

Ichinose H, Ohye T, Yokochi M, Fujita K, Nagatsu T. Ichinose H, et al. Neurosci Lett. 1995 May 5;190(2):140-2. doi: 10.1016/0304-3940(95)11511-t. Neurosci Lett. 1995. PMID: 7644124

4

Characterization of mouse and human GTP cyclohydrolase I genes. Mutations in patients with GTP cyclohydrolase I deficiency.

Ichinose H, Ohye T, Matsuda Y, Hori T, Blau N, Burlina A, Rouse B, Matalon R, Fujita K, Nagatsu T. Ichinose H, et al. J Biol Chem. 1995 Apr 28;270(17):10062-71. doi: 10.1074/jbc.270.17.10062. J Biol Chem. 1995. PMID: 7730309 Free article.

Previously, we reported three species of human GTP cyclohydrolase I cDNA in a human liver cDNA library (Togari, A., Ichinose, H., Matsumoto, S., Fujita, K., and Nagatsu, T. (1992) Biochem. ...Furthermore, very recently, we found that the GTP cyclohydrolase I gene is …

Previously, we reported three species of human GTP cyclohydrolase I cDNA in a human liver cDNA library (Togari, A., Ichinose, H …

5

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene.

Ichinose H, Ohye T, Takahashi E, Seki N, Hori T, Segawa M, Nomura Y, Endo K, Tanaka H, Tsuji S, et al. Ichinose H, et al. Nat Genet. 1994 Nov;8(3):236-42. doi: 10.1038/ng1194-236. Nat Genet. 1994. PMID: 7874165

6

Cloning and sequencing of cDNA encoding mouse GTP cyclohydrolase I.

Nomura T, Ichinose H, Sumi-Ichinose C, Nomura H, Hagino Y, Fujita K, Nagatsu T. Nomura T, et al. Among authors: ichinose h. Biochem Biophys Res Commun. 1993 Mar 15;191(2):523-7. doi: 10.1006/bbrc.1993.1249. Biochem Biophys Res Commun. 1993. PMID: 8461009

7

Isolation of a full-length cDNA clone for human GTP cyclohydrolase I type 1 from pheochromocytoma.

Nomura T, Ohtsuki M, Matsui S, Sumi-Ichinose C, Nomura H, Hagino Y, Iwase K, Ichinose H, Fujita K, Nagatsu T. Nomura T, et al. Among authors: ichinose h. J Neural Transm Gen Sect. 1995;101(1-3):237-42. doi: 10.1007/BF01271561. J Neural Transm Gen Sect. 1995. PMID: 8695054

8

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

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

9

GTP cyclohydrolase I gene, tetrahydrobiopterin, and tyrosine hydroxylase gene: their relations to dystonia and parkinsonism.

Nagatsu T, Ichinose H. Nagatsu T, et al. Among authors: ichinose h. Neurochem Res. 1996 Feb;21(2):245-50. doi: 10.1007/BF02529141. Neurochem Res. 1996. PMID: 9182249 Review.

10

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

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

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