Ai Hattori

Nagoya, Japan

Last Updated: 09/26/2026

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Found 11 publications

Iron overload patients with unknown etiology from national survey in Japan.

Iron overload patients with unknown etiology from national survey in Japan.

Journal: International journal of hematology

Published: August 21, 2016

A Single Amino Acid Mutation Converts (R)-5-Diphosphomevalonate Decarboxylase into a Kinase.

A Single Amino Acid Mutation Converts (R)-5-Diphosphomevalonate Decarboxylase into a Kinase.

Journal: The Journal of biological chemistry

Published: August 08, 2016

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.

Journal: International journal of hematology

Published: January 23, 2016

In Vivo Formation of the Protein Disulfide Bond That Enhances the Thermostability of Diphosphomevalonate Decarboxylase, an Intracellular Enzyme from the Hyperthermophilic Archaeon Sulfolobus solfataricus.

In Vivo Formation of the Protein Disulfide Bond That Enhances the Thermostability of Diphosphomevalonate Decarboxylase, an Intracellular Enzyme from the Hyperthermophilic Archaeon Sulfolobus solfataricus.

Journal: Journal of bacteriology

Published: May 07, 2015

Biochemical staging of the chronic hepatic lesions of Wilson disease.

Biochemical staging of the chronic hepatic lesions of Wilson disease.

Journal: Nagoya journal of medical science

Published: August 19, 2014

(R)-mevalonate 3-phosphate is an intermediate of the mevalonate pathway in Thermoplasma acidophilum.

(R)-mevalonate 3-phosphate is an intermediate of the mevalonate pathway in Thermoplasma acidophilum.

Journal: The Journal of biological chemistry

Published: April 24, 2014

A male patient with ferroportin disease B and a female patient with iron overload similar to ferroportin disease B.

A male patient with ferroportin disease B and a female patient with iron overload similar to ferroportin disease B.

Journal: Clinical journal of gastroenterology

Published: November 05, 2013

Iron chelation therapy for a case of transfusion-independent MDS-RARS with significant iron overload.

Iron chelation therapy for a case of transfusion-independent MDS-RARS with significant iron overload.

Journal: International journal of hematology

Published: October 22, 2012

Clinicopathological study of Japanese patients with genetic iron overload syndromes.

Clinicopathological study of Japanese patients with genetic iron overload syndromes.

Journal: Pathology international

Published: August 29, 2012

Various copper and iron overload patterns in the livers of patients with Wilson disease and idiopathic copper toxicosis.

Various copper and iron overload patterns in the livers of patients with Wilson disease and idiopathic copper toxicosis.

Journal: Medical molecular morphology

Published: February 01, 2012

Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.

Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.

Journal: Blood cells, molecules & diseases

Published: November 18, 2011

Showing 1-11 of 11

Last Updated: 09/26/2026