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Publications by Minako Hino

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

Hemoglobin

Biochemistry

Genetics

Clinical Biochemistry

Hematology

2012

English

Related publications

Fructosuria and Recurrent Hypoglycemia in a Patient With a Novel C.1693T>A Variant in the 3′ Untranslated Region of the Aldolase B Gene

SAGE Open Medical Case Reports

2019

English

Β Globin Mutations in Turkish, Northern Iraqi and Albanian Patients With Β Thalassemia Major

Thalassemia Reports

2018

English

Modifiers of Γ-Globin Gene Expression and Treatment of Β-Thalassemia

2015

English

A Preclinical Approach for Gene Therapy of Β-Thalassemia

Annals of the New York Academy of Sciences

Philosophy of Science

2010

English

Computational Analysis of Protein Structure Changes as a Result of Nondeletion Insertion Mutations in Human Β-Globin Gene Suggests Possible Cause of Β-Thalassemia

BioMed Research International

English

Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree

Molecular Medicine Reports

English

Β-Thalassemia Mutation at Codon 37 (TGG>>TGA) Detected in a Turkish Family

Turkish Journal of Haematology

Hematology

2013

English

Compound Heterozygous Hemophilia a in a Female Patient and the Identification of a Novel Missense Mutation, p.Met1093Ile

Molecular Medicine Reports

English

Two Novel C-Terminal Frameshift Mutations in the Β-Globin Gene Lead to Rapid mRNA Decay

BMC Medical Genetics

Genetics

2017

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Minako Hino

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

Related publications

Fructosuria and Recurrent Hypoglycemia in a Patient With a Novel C.1693T>A Variant in the 3′ Untranslated Region of the Aldolase B Gene

Β Globin Mutations in Turkish, Northern Iraqi and Albanian Patients With Β Thalassemia Major

Modifiers of Γ-Globin Gene Expression and Treatment of Β-Thalassemia

A Preclinical Approach for Gene Therapy of Β-Thalassemia

Computational Analysis of Protein Structure Changes as a Result of Nondeletion Insertion Mutations in Human Β-Globin Gene Suggests Possible Cause of Β-Thalassemia

Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree

Β-Thalassemia Mutation at Codon 37 (TGG>>TGA) Detected in a Turkish Family

Compound Heterozygous Hemophilia a in a Female Patient and the Identification of a Novel Missense Mutation, p.Met1093Ile

Two Novel C-Terminal Frameshift Mutations in the Β-Globin Gene Lead to Rapid mRNA Decay