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Naohiko Seki

Researcher at Chiba University

Publications -  391
Citations -  20245

Naohiko Seki is an academic researcher from Chiba University. The author has contributed to research in topics: microRNA & Cancer. The author has an hindex of 74, co-authored 381 publications receiving 18648 citations. Previous affiliations of Naohiko Seki include Toho University & National Institute of Radiological Sciences.

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Chromosome mapping of RNF16 and Rnf16, human, mouse and rat genes coding for testis RING finger protein (terf), a member of the RING finger family

TL;DR: Results provide additional evidence that the mouse 11B region displays conserved linkage homology with the rat 10q22 region, whereas in the case of RNF16, this homology is only conserved among rodents, distinct from the 1q42 region of the human genome.
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Chromosome abnormalities and rare fragile sites detected in azoospermia patients

TL;DR: The overall frequency of distamycin A-inducible fragile sites in azoospermia patients appeared to be higher than those reported for Japanese healthy subjects and cancer patients, however, no significant relation among fragile sites, clinical and histological findings has been detected so far.
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Isolation of human purH gene expressed in the rodent transformant cells by subtractive enrichment of 3'-untranslated region of human transcript.

TL;DR: A subtraction procedure was developed for identification and isolation of a human gene transcribed in mouse transformant cells and recovered the human purH gene from a mice transformant cell line, which was originally established by functional complementation using the human metaphase chromosome-mediated gene transfer technique.
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Comparing gene expression profiles in human liver, gastric, and pancreatic tissues using full-length-enriched cDNA libraries

TL;DR: The results suggest that functional differences between tissues are probably related to their divergent gene expression profiles, and form a basis for understanding the molecular mechanisms underlying tissue-specific pathogenesis that are expressed in different organs.
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Construction of YAC Contigs at Human Chromosome 11q22.3–q23.1 Region Covering the Ataxia Telangiectasia Locus

TL;DR: In this paper, the major AT loci, AT-A and AT-C, are shown to be closely linked at chromosome Ilq22-q23.1 and include the entire region of the major Ataxia telangiectasia (AT) between D11S1819 and D11 S1818.