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Kazuo Nishigaki

Researcher at University of Tokyo

Publications -  6
Citations -  84

Kazuo Nishigaki is an academic researcher from University of Tokyo. The author has contributed to research in topics: Enhancer & Long terminal repeat. The author has an hindex of 4, co-authored 6 publications receiving 77 citations.

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Molecular characteristics of malignant lymphomas in cats naturally infected with feline immunodeficiency virus

TL;DR: Results indicated that FIV might not play a direct role in tumorigenesis of lymphoma in cats and that no consistent tumor type was found in lymphoma cases infected with FIV.
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Structure and function of the long terminal repeats of feline leukemia viruses derived from naturally occurring acute myeloid leukemias in cats.

TL;DR: Long terminal repeats of feline leukemia viruses cloned from feline acute myeloid leukemias frequently contained direct repeats of 40 to 74 bp in the upstream region of the enhancer (URE), suggesting its association with tumorigenic potential in myeloids cells.
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Clinicopathological and immunological characteristics of six cats with granular lymphocyte tumors

TL;DR: Findings indicated that feline GL tumors can be considered as a specific disease entity in feline lymphomas because the cases examined in this study showed onset at an older age, a low incidence of FeLV infection and frequent involvement of gastrointestinal lesions, which are not found in typical FeLV-associated lymphomas.
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Cloning and chromosome mapping of the feline genes p21waf1 and p27kip1

TL;DR: RT-PCR/SSCP (single strand conformation polymorphism) analysis of p27Kip1 cDNA did not uncover any amino acid substitutions in the 10 feline leukemia and lymphoma cases that were examined, andSouthern-blot analyses of 17 feline spontaneous leukemia andymphoma cases using these cDNAs as probes did not reveal any rearrangements in either the p21WAF1 or the p27kip1 gene.
Journal Article

Regulation of gene expression directed by the long terminal repeats of feline leukemia viruses.

TL;DR: The present study revealed the strong promoter activity of the FeLV LTR with 3 enhancer repeats and its modular enhancer elements positively regulating the transcription in a relatively tissue-specific manner.