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Takao Sekiya

Researcher at National Cancer Research Institute

Publications -  120
Citations -  12555

Takao Sekiya is an academic researcher from National Cancer Research Institute. The author has contributed to research in topics: Gene & Loss of heterozygosity. The author has an hindex of 39, co-authored 120 publications receiving 12461 citations. Previous affiliations of Takao Sekiya include University of Tokyo.

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Journal ArticleDOI

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

TL;DR: The mobility shift analysis of single-stranded DNAs on neutral polyacrylamide gel electrophoresis to detect DNA polymorphisms was developed and SSCPs were found to be allelic variants of true Mendelian traits, and therefore they should be useful genetic markers.
Journal ArticleDOI

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

TL;DR: It is found that most single base changes in up to 200-base fragments could be detected as mobility shifts and the interspersed repetitive sequences of human, Alu repeats are highly polymorphic.
Book ChapterDOI

Detection of p53 Gene Mutations in Human Brain Tumors by Single-strand Conformation Polymorphism Analysis of Polymerase Chain Reaction Products

TL;DR: Results suggested that aberrations of the p53 gene were not correlated with the malignancy of some types of brain tumors such as anaplastic astrocytoma and glioblastoma, contrary to previous observations on colorectal cancers.
Journal ArticleDOI

TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer.

TL;DR: This region contains a single confirmed gene, TSLC1, whose expression is reduced or absent in A549 and several other NSCLC, hepatocellular carcinoma (HCC) and pancreatic cancer (PaC) cell lines, and is correlated with promoter methylation state in these cell lines.
Journal Article

Deletions of Chromosome 13q, Mutations in Retinoblastoma 1, and Retinoblastoma Protein State in Human Hepatocellular Carcinoma

TL;DR: The results indicate that the loss of a region of chromosome 13q including the RB1 locus significantly correlates with loss of RB protein in hepatocellular carcinomas, however, tumor-specific mutations of theRB1 gene were detected in only two of 13 tumors with LOH and/or lack of RBprotein expression, indicating that analysis of the RB 1 status at the protein level in these tumors may be more sensitive than the actual mutational analysis.