R. Morita

发表

Mutations in EFHC1 cause juvenile myoclonic epilepsy

M. T. Medina, K. Yamakawa, J. Inazawa, 2004, Nature Genetics.

Direct Metagenomic Detection of Viral Pathogens in Nasal and Fecal Specimens Using an Unbiased High-Throughput Sequencing Approach

J. Kawai, Y. Hayashizaki, N. Maeda, 2009, PloS one.

Novel polymorphisms in the promoter region of the neurotrophin-3 gene and their associations with schizophrenia.

K. Yamakawa, Hiroshi Tanaka, S. Nanko, 2002, American journal of medical genetics.

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

Y. Nakamura, R. Morita, Y. Nakamura, 1991, Cancer research.

A novel gene in the chromosomal region for juvenile myoclonic epilepsy on 6p12 encodes a brain-specific lysosomal membrane protein.

K. Yamakawa, K. Agarwala, J. Inazawa, 2001, Biochemical and biophysical research communications.

Renal Cell Carcinoma Common Regions of Deletion on Chromosomes 5 q , 6 q , and 10 q Updated

Yusuke Nakamura, O. Yoshida, O. Ogawa, 2006 .

Allelotype of Human Ovarian Cancer 1

Yusuke Nakamura, R. Morita, H. Saito, 2006 .

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

Y. Nakamura, M. Lathrop, R. Morita, 1991, Genomics.

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

Y. Nakamura, O. Yoshida, O. Ogawa, 1991, Cancer research.

Recent Developments in the Quest for Myoclonic Epilepsy Genes

M. T. Medina, K. Yamakawa, A. Delgado-Escueta, 2003, Epilepsia.

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

Antonio V. Delgado-Escueta, Julia N. Bailey, M. T. Medina, 2002, Epilepsy Research.

Allelotype of human ovarian cancer.

Y. Nakamura, T. Sato, J. H. Lee, 1991, Cancer research.

Allelotype of renal cell carcinoma.

Y. Nakamura, S. Maeda, S. Kamidono, 1991, Cancer research.

Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy

M. T. Medina, K. Yamakawa, J. Inazawa, 2006, Neuroscience Letters.

Allelotype of Renal Cell Carcinoma1

Yusuke Nakamura, S. Maeda, S. Kamidono, 2006 .

JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.

K. Yamakawa, X. Chen, J. Korenberg, 1998, Biochemical and biophysical research communications.

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

K. Yamakawa, P. Shah, I. Castroviejo, 2000, Genomics.

Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.

M. T. Medina, K. Yamakawa, A. Delgado-Escueta, 2002, American journal of medical genetics.

[Juvenile myoclonic epilepsy in chromosome 6p12: clinical and genetic advances].

M. T. Medina, K. Yamakawa, A. Delgado-Escueta, 2002, Revista de neurologia.

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

K. Yamakawa, P. Shah, I. Castroviejo, 1999, Epilepsy Research.

Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic features.

M. T. Medina, I. Castroviejo, G. Pineda, 2005, Advances in neurology.

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

K. Yamakawa, P. Shah, A. Delgado-Escueta, 2001, Epilepsy Research.