Morita R - Search Results

1

Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma.

Morita R, Saito S, Ishikawa J, Ogawa O, Yoshida O, Yamakawa K, Nakamura Y. Morita R, et al. Cancer Res. 1991 Nov 1;51(21):5817-20. Cancer Res. 1991. PMID: 1682036

2

Allelotype of human ovarian cancer.

Sato T, Saito H, Morita R, Koi S, Lee JH, Nakamura Y. Sato T, et al. Among authors: morita r. Cancer Res. 1991 Oct 1;51(19):5118-22. Cancer Res. 1991. PMID: 1655245

3

Allelotype of renal cell carcinoma.

Morita R, Ishikawa J, Tsutsumi M, Hikiji K, Tsukada Y, Kamidono S, Maeda S, Nakamura Y. Morita R, et al. Cancer Res. 1991 Feb 1;51(3):820-3. Cancer Res. 1991. PMID: 1670999

4

A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma.

Yamakawa K, Morita R, Takahashi E, Hori T, Ishikawa J, Nakamura Y. Yamakawa K, et al. Among authors: morita r. Cancer Res. 1991 Sep 1;51(17):4707-11. Cancer Res. 1991. PMID: 1678685

5

[Tumor suppressor genes associated with development of human renal cell carcinoma].

Morita R, Hikiji K, Yamakawa K, Nakamura Y. Morita R, et al. Nihon Rinsho. 1992 Dec;50(12):3100-5. Nihon Rinsho. 1992. PMID: 1491460 Review. Japanese.

6

A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3.

Yamakawa K, Morita R, Takahashi E, Hori T, Lathrop M, Nakamura Y. Yamakawa K, et al. Among authors: morita r. Genomics. 1991 Nov;11(3):565-72. doi: 10.1016/0888-7543(91)90063-k. Genomics. 1991. PMID: 1685476

7

Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.

Suzuki T, Morita R, Sugimoto Y, Sugawara T, Bai DS, Alonso ME, Medina MT, Bailey JN, Rasmussen A, Ramos-Peek J, Cordova S, Rubio-Donnadieu F, Ochoa A, Jara-Prado A, Inazawa J, Delgado-Escueta AV, Yamakawa K. Suzuki T, et al. Among authors: morita r. Epilepsy Res. 2002 Aug;50(3):265-75. doi: 10.1016/s0920-1211(02)00052-9. Epilepsy Res. 2002. PMID: 12200217

8

Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24.

Morita R, Miyazaki E, Shah PU, Castroviejo IP, Delgado-Escueta AV, Yamakawa K. Morita R, et al. Epilepsy Res. 1999 Nov;37(2):151-8. doi: 10.1016/s0920-1211(99)00061-3. Epilepsy Res. 1999. PMID: 10510981 Clinical Trial.

9

T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients.

Sugimoto Y, Morita R, Amano K, Shah PU, Pascual-Castroviejo I, Khan S, Delgado-Escueta AV, Yamakawa K. Sugimoto Y, et al. Among authors: morita r. Epilepsy Res. 2001 Aug;46(2):139-44. doi: 10.1016/s0920-1211(01)00274-1. Epilepsy Res. 2001. PMID: 11463515

10

Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map.

Sugimoto Y, Morita R, Amano K, Fong CY, Shah PU, Castroviejo IP, Khan S, Delgado-Escueta AV, Yamakawa K. Sugimoto Y, et al. Among authors: morita r. Genomics. 2000 Sep 15;68(3):264-72. doi: 10.1006/geno.2000.6296. Genomics. 2000. PMID: 10995568

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