Takenori Nitta

Ube, Japan

Last Updated: 09/26/2026

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Found 8 publications

A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin.

A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin.

Journal: Hemoglobin
Published: March 08, 2018

A new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.

A new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.

Journal: Hemoglobin
Published: February 19, 2015

The interference by HbF on HbA1c (BM Test HbA1c) measurement in enzymatic method.

The interference by HbF on HbA1c (BM Test HbA1c) measurement in enzymatic method.

Journal: Annals of clinical biochemistry
Published: December 21, 2014

Oxidation status of β-thalassemia minor and Hb H disease, and its association with glycerol lysis time (GLT50).

Oxidation status of β-thalassemia minor and Hb H disease, and its association with glycerol lysis time (GLT50).

Journal: Hemoglobin
Published: March 12, 2014

A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene.

A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon gene.

Journal: Hemoglobin
Published: April 23, 2013

Establishment of multiplex hybri-probe method--analysis using the polymorphism of UGT1A1 gene

Establishment of multiplex hybri-probe method--analysis using the polymorphism of UGT1A1 gene

Journal: Rinsho byori. The Japanese journal of clinical pathology
Published: August 14, 2012

The +1,506 (A>C) mutation in the 3' untranslated region affects β-globin expression.

The +1,506 (A>C) mutation in the 3' untranslated region affects β-globin expression.

Journal: Hemoglobin
Published: June 28, 2012

Identification of a novel mutation in the β-globin gene 3' untranslated region [+1,506 (A>C)] in a Japanese male with a heterozygous β-thalassemia phenotype.

Identification of a novel mutation in the β-globin gene 3' untranslated region [+1,506 (A>C)] in a Japanese male with a heterozygous β-thalassemia phenotype.

Journal: Hemoglobin
Published: January 06, 2012
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Last Updated: 09/26/2026