Akira Sano

Kagoshima, 8908760, Japan

Last Updated: 09/26/2026

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Found 30 publications

Endolysosomal iron-associated vesicular changes and ferroptosis-related vulnerability in VPS13A-knockdown cells.

Endolysosomal iron-associated vesicular changes and ferroptosis-related vulnerability in VPS13A-knockdown cells.

Journal: Molecular biology reports

Published: June 09, 2026

Chorein deficiency promotes ferroptosis.

Chorein deficiency promotes ferroptosis.

Journal: FEBS open bio

Published: January 09, 2024

The Role of Chorein Deficiency in Late Spermatogenesis.

The Role of Chorein Deficiency in Late Spermatogenesis.

Journal: Biomedicines

Published: January 03, 2024

Aging-Related Catatonia with Reversible Dopamine Transporter Dysfunction in Females with Depressive Symptoms: A Case Series.

Aging-Related Catatonia with Reversible Dopamine Transporter Dysfunction in Females with Depressive Symptoms: A Case Series.

Journal: The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry

Published: April 07, 2023

Predicting postpartum depression by evaluating temperament during pregnancy.

Predicting postpartum depression by evaluating temperament during pregnancy.

Journal: Journal of affective disorders

Published: January 06, 2021

Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A.

Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A.

Journal: Journal of human genetics

Published: November 13, 2020

Correction to: Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation.

Correction to: Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation.

Journal: Journal of human genetics

Published: October 20, 2020

Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.

Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.

Journal: Journal of human genetics

Published: October 12, 2020

Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation.

Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation.

Journal: Journal of human genetics

Published: July 27, 2020

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A.

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A.

Journal: Journal of human genetics

Published: June 04, 2020

Novel VPS13A Gene Mutations in a South Asian, Indian Patient with Chorea‑acanthocytosis.

Novel VPS13A Gene Mutations in a South Asian, Indian Patient with Chorea‑acanthocytosis.

Journal: Neurology India

Published: March 05, 2020

Chorea-acanthocytosis with a novel mutation in the vacuolar protein sorting 13 homolog a gene: A case report.

Chorea-acanthocytosis with a novel mutation in the vacuolar protein sorting 13 homolog a gene: A case report.

Journal: Journal of the neurological sciences

Published: December 09, 2019

Showing 1-12 of 30

Last Updated: 09/26/2026