Hori T - Search Results

1

Chromosomal localization of the epsilon 1, epsilon 3 and zeta 1 subunit genes of the human NMDA receptor channel.

Takano H, Onodera O, Tanaka H, Mori H, Sakimura K, Hori T, Kobayashi H, Mishina M, Tsuji S. Takano H, et al. Among authors: hori t. Biochem Biophys Res Commun. 1993 Dec 15;197(2):922-6. doi: 10.1006/bbrc.1993.2567. Biochem Biophys Res Commun. 1993. PMID: 8267632

2

Structure, chromosomal location, and expression profile of EXTR1 and EXTR2, new members of the multiple exostoses gene family.

Saito T, Seki N, Yamauchi M, Tsuji S, Hayashi A, Kozuma S, Hori T. Saito T, et al. Among authors: hori t. Biochem Biophys Res Commun. 1998 Feb 4;243(1):61-6. doi: 10.1006/bbrc.1997.8062. Biochem Biophys Res Commun. 1998. PMID: 9473480

3

Chromosome mapping of the human (RECA) and mouse (Reca) homologs of the yeast RAD51 and Escherichia coli recA genes to human (15q15.1) and mouse (2F1) chromosomes by direct R-banding fluorescence in situ hybridization.

Takahashi E, Matsuda Y, Hori T, Yasuda N, Tsuji S, Mori M, Yoshimura Y, Yamamoto A, Morita T, Matsushiro A. Takahashi E, et al. Among authors: hori t. Genomics. 1994 Jan 15;19(2):376-8. doi: 10.1006/geno.1994.1074. Genomics. 1994. PMID: 8188269

4

[Chromosomal fragile sites].

Hori T, Yamauchi M, Tsuji S. Hori T, et al. Tanpakushitsu Kakusan Koso. 1996 Nov;41(15 Suppl):2315-24. Tanpakushitsu Kakusan Koso. 1996. PMID: 8952394 Review. Japanese. No abstract available.

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. Among authors: hori t. Nat Genet. 1994 Nov;8(3):236-42. doi: 10.1038/ng1194-236. Nat Genet. 1994. PMID: 7874165

6

A distamycin A-inducible fragile site, FRA8E, located in the region of the hereditary multiple exostoses gene, is not involved in HPV16 DNA integration and amplification.

Hori T, Seki N, Ohira M, Saito T, Yamauchi M, Sagara M, Hayashi A, Tsuji S, Ito H, Imai T. Hori T, et al. Cancer Genet Cytogenet. 1998 Feb;101(1):24-34. doi: 10.1016/s0165-4608(97)00222-7. Cancer Genet Cytogenet. 1998. PMID: 9460496

7

Topographic mapping of EEG spectral power and coherence in delta activity during the transition from wakefulness to sleep.

Tanaka H, Hayashi M, Hori T. Tanaka H, et al. Among authors: hori t. Psychiatry Clin Neurosci. 1999 Apr;53(2):155-7. doi: 10.1046/j.1440-1819.1999.00509.x. Psychiatry Clin Neurosci. 1999. PMID: 10459676 Free article.

8

Topographic mapping of electroencephalography coherence in hypnagogic state.

Tanaka H, Hayashi M, Hori T. Tanaka H, et al. Among authors: hori t. Psychiatry Clin Neurosci. 1998 Apr;52(2):147-8. doi: 10.1111/j.1440-1819.1998.tb00998.x. Psychiatry Clin Neurosci. 1998. PMID: 9628119 Free article.

9

Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families.

Hori T, Yamauchi M, Seki N, Tsuji S, Kondo I. Hori T, et al. Clin Genet. 1993 Jan;43(1):34-8. doi: 10.1111/j.1399-0004.1993.tb04423.x. Clin Genet. 1993. PMID: 8462194

10

Statistical features of hypnagogic EEG measured by a new scoring system.

Tanaka H, Hayashi M, Hori T. Tanaka H, et al. Among authors: hori t. Sleep. 1996 Nov;19(9):731-8. doi: 10.1093/sleep/19.9.731. Sleep. 1996. PMID: 9122561

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