K. Koyama

发表

Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients.

K. Kinzler, B. Vogelstein, Y. Nakamura, 1991, Science.

Identification of seven genes regulated by wild-type p53 in a colon cancer cell line carrying a well-controlled wild-type p53 expression system.

Y. Nakamura, M. Monden, H. Arakawa, 1999, Oncology research.

Identification of a brain-specific APC homologue, APCL, and its interaction with beta-catenin.

Y. Nakamura, A. Fujiyama, T. Akiyama, 1998, Cancer research.

The human homologue of the murine Llglh gene (LLGL) maps within the Smith-Magenis syndrome region in 17p11.2.

Y. Nakamura, J. Inazawa, N. Takahashi, 1996, Cytogenetics and cell genetics.

A 3‐Mb physical map of the chromosome region 8p21.3‐p22, including a 600‐kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer, and non‐small cell lung cancer

Yusuke Nakamura, M. Oshimura, M. Emi, 1994, Genes, chromosomes & cancer.

Isolation of a novel gene on 8p21.3-22 whose expression is reduced significantly in human colorectal cancers with liver metastasis.

Y. Nakamura, H. Nakagawa, Y. Miyoshi, 2000, Genes, chromosomes & cancer.

Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3

Yusuke Nakamura, Toshihiro Tanaka, M. Monden, 1998, Human Genetics.

Isolation of a candidate tumor suppressor gene on chromosome 8p21.3-p22 that is homologous to an extracellular domain of the PDGF receptor beta gene.

Y. Nakamura, M. Monden, T. Kuroki, 1995, Oncogene.

Isolation of a novel gene on 8p21.3–22 whose expression is reduced significantly in human colorectal cancers with liver metastasis

Yusuke Nakamura, H. Nakagawa, Y. Miyoshi, 2000 .

Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers

M. Monden, Y. Miyoshi, S. Okamura, 1998, Journal of Human Genetics.

Effect of islet-activating protein (IAP) upon insulin secretion from human pancreatic islets.

N. Nakamura, T. Yoshida, Y. Nakamura, 1981, Endocrinologia japonica.

The cell adhesion regulator (CAR) gene, TaqI and insertion/deletion polymorphisms, and regional assignment to the peritelomeric region of 16q by linkage analysis.

Y. Nakamura, M. Emi, K. Koyama, 1993, Genomics.

Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification

Yusuke Nakamura, K. Koyama, S. Usami, 2003, Journal of Human Genetics.

Analysis of APCL, a Brain‐specific Adenomatous Polyposis Coli Homologue, for Mutations and Expression in Brain Tumors

Yusuke Nakamura, M. Monden, H. Nakagawa, 1999, Japanese journal of cancer research : Gann.

Germline mutations of the RET proto-oncogene in eight Japanese patients with multiple endocrine neoplasia type 2A (MEN2A)

Yusuke Nakamura, A. Miyauchi, T. Wakasugi, 1995, Human Genetics.

Isolation of 115 human chromosome 8-specific expressed-sequence tags by exon amplification.

Y. Nakamura, K. Koyama, K. Sudo, 1995, Genomics.

EB3, a novel member of the EB1 family preferentially expressed in the central nervous system, binds to a CNS-specific APC homologue

Yusuke Nakamura, T. Akiyama, H. Nakagawa, 2000, Oncogene.

Comparative FISH mapping of the ancestral fusion point of human chromosome 2

Yusuke Nakamura, K. Tokunaga, M. Hirai, 2004, Chromosome Research.

A high-resolution cytogenetic map of human chromosome 12: Localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridization

Yusuke Nakamura, K. Koyama, E. Takahashi, 1993, Human Genetics.

A high-resolution cytogenetic map of human chromosome 2: localization of 434 cosmid markers by direct R-banding fluorescence in situ hybridization.

Y. Nakamura, M. Hirai, K. Koyama, 1995, Cytogenetics and cell genetics.

Cloning of translocation breakpoints associated with Shwachman syndrome and identification of a candidate gene

Y. Makita, H. Ohashi, S. Ikegawa, 1999, Clinical genetics.

Detailed analysis of genetic alterations in colorectal tumors from patients with and without familial adenomatous polyposis (FAP).

M. Emi, Y. Miyoshi, J. Utsunomiya, 1993, Oncogene.

Frameshift Mutation of the STK11 Gene in a Sporadic Gastrointestinal Cancer with Microsatellite Instability

Yusuke Nakamura, M. Monden, H. Nakagawa, 1999, Japanese journal of cancer research : Gann.

Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome

Y. Nakamura, M. Monden, M. Watatani, 1998, Human Genetics.

The brain finger protein gene (ZNF179), a member of the RING finger family, maps within the Smith-Magenis syndrome region at 17p11.2.

Y. Nakamura, S. Inoue, J. Inazawa, 1997, American journal of medical genetics.

Isolation and characterization of a novel TP53‐inducible gene, TP53TG3

S. Okamura, C. Ng, Y. Takei, 1999, Genes, chromosomes & cancer.

Isolation and characterization of a novel TP53‐inducible gene, TP53TG5, which suppresses growth and shows cell cycle‐dependent transition of expression

Y. Nakamura, T. Tokino, Y. Miyoshi, 2000, Genes, chromosomes & cancer.

Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization

Y. Nakamura, J. Inazawa, C. Sakakura, 1999, British Journal of Cancer.

Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI

Y. Nakamura, M. Monden, Y. Miyoshi, 1998, Cytogenetic and Genome Research.

APCL, a central nervous system-specific homologue of adenomatous polyposis coli tumor suppressor, binds to p53-binding protein 2 and translocates it to the perinucleus.

Y. Nakamura, T. Akiyama, H. Nakagawa, 2000, Cancer Research.

VNTR (variable number of tandem repeat) sequences as transcriptional, translational, or functional regulators

Yusuke Nakamura, Yusuke Nakamura, K. Koyama, 1998, Journal of Human Genetics.

Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses

N. Niikawa, Y. Nakamura, J. Inazawa, 1994, Genes, chromosomes & cancer.

Isolation and mapping of 328 new cosmid markers on human chromosome 8: construction of a high-resolution cytogenetic map of chromosome 8 with 416 markers.

Y. Nakamura, K. Koyama, E. Takahashi, 1994, Cytogenetics and cell genetics.

Isolation and mapping of 88 new RFLP markers on human chromosome 8.

Y. Nakamura, M. Oshimura, M. Emi, 1992, Genomics.

VNTR sequence on human chromosome 11p15 that affects transcriptional activity

Yusuke Nakamura, K. Koyama, Shuichi Iwashita, 2001, Journal of Human Genetics.

Identification and characterization of a cDNA, which is highly homologous to the ribonucleoprotein gene, from a locus (D1OS102) closely linked to MEN2 (multiple endocrine neoplasia type 2)

A. Tanigami, Yusuke Nakamura, T. Tokino, 1993 .

A 3‐Mb physical map of the chromosome region 8p21.3‐p22, including a 600‐kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer, and non‐small cell lung cancer

Yusuke Nakamura, M. Oshimura, M. Emi, 1994, Genes, chromosomes & cancer.

Mapping of the human nicotinic acetylcholine receptor beta 3 gene (CHRNB3) within chromosome 8p11.2.

Y. Nakamura, K. Koyama, K. Sudo, 1994, Genomics.

Expression of Apc2 during mouse development.

Yusuke Nakamura, H. Yamanaka, K. Noguchi, 2002, Brain research. Gene expression patterns.