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A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach

A modified AFLP (amplified fragment length polymorphism) method was employed to isolate genes differentially expressed in renal carcinogenesis of Tsc2 gene mutant (Eker) rats. One gene, selected for further investigation, was named “Niban” (“second” in Japanese), because it is the second new gene to...

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Autores principales: Majima, Shuichi, Kajino, Kazunori, Fukuda, Tomokazu, Otsuka, Fujio, Hino, Okio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926447/
https://www.ncbi.nlm.nih.gov/pubmed/11011112
http://dx.doi.org/10.1111/j.1349-7006.2000.tb01027.x
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author Majima, Shuichi
Kajino, Kazunori
Fukuda, Tomokazu
Otsuka, Fujio
Hino, Okio
author_facet Majima, Shuichi
Kajino, Kazunori
Fukuda, Tomokazu
Otsuka, Fujio
Hino, Okio
author_sort Majima, Shuichi
collection PubMed
description A modified AFLP (amplified fragment length polymorphism) method was employed to isolate genes differentially expressed in renal carcinogenesis of Tsc2 gene mutant (Eker) rats. One gene, selected for further investigation, was named “Niban” (“second” in Japanese), because it is the second new gene to be found after Erc (expressed in renal carcinoma) in our laboratory. Importantly, “Niban” is well expressed even in small primary rat Eker renal tumors, more than in progressed cell lines, and is also expressed in human renal carcinoma cells, but not in normal human or rat kidneys. Chromosome assignment was to RNO 13 in the rat, and HSA 1. This “Niban” gene is a candidate as a marker for renal tumor, especially early‐stage renal carcinogenesis.
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spelling pubmed-59264472018-05-11 A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach Majima, Shuichi Kajino, Kazunori Fukuda, Tomokazu Otsuka, Fujio Hino, Okio Jpn J Cancer Res Rapid Communication A modified AFLP (amplified fragment length polymorphism) method was employed to isolate genes differentially expressed in renal carcinogenesis of Tsc2 gene mutant (Eker) rats. One gene, selected for further investigation, was named “Niban” (“second” in Japanese), because it is the second new gene to be found after Erc (expressed in renal carcinoma) in our laboratory. Importantly, “Niban” is well expressed even in small primary rat Eker renal tumors, more than in progressed cell lines, and is also expressed in human renal carcinoma cells, but not in normal human or rat kidneys. Chromosome assignment was to RNO 13 in the rat, and HSA 1. This “Niban” gene is a candidate as a marker for renal tumor, especially early‐stage renal carcinogenesis. Blackwell Publishing Ltd 2000-09 /pmc/articles/PMC5926447/ /pubmed/11011112 http://dx.doi.org/10.1111/j.1349-7006.2000.tb01027.x Text en
spellingShingle Rapid Communication
Majima, Shuichi
Kajino, Kazunori
Fukuda, Tomokazu
Otsuka, Fujio
Hino, Okio
A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach
title A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach
title_full A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach
title_fullStr A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach
title_full_unstemmed A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach
title_short A Novel Gene “Niban” Upregulated in Renal Carcinogenesis: Cloning by the cDNA‐amplified Fragment Length Polymorphism Approach
title_sort novel gene “niban” upregulated in renal carcinogenesis: cloning by the cdna‐amplified fragment length polymorphism approach
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926447/
https://www.ncbi.nlm.nih.gov/pubmed/11011112
http://dx.doi.org/10.1111/j.1349-7006.2000.tb01027.x
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