Tetsuaki Kimura

Obu, 4748511, Japan

Last Updated: 09/26/2026

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Found 22 publications

Linked genetic loci and genotype-dependent temperature effects shape craniofacial morphology in medaka.

Linked genetic loci and genotype-dependent temperature effects shape craniofacial morphology in medaka.

Journal: G3 (Bethesda, Md.)

Published: February 03, 2026

MIT/TFE family transcription factors, Mitf and Tfec, redundantly promote pigment cell differentiation and retinal epithelium pigmentation in teleosts.

MIT/TFE family transcription factors, Mitf and Tfec, redundantly promote pigment cell differentiation and retinal epithelium pigmentation in teleosts.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists

Published: October 07, 2025

A genetic model of congenital intestinal atresia implicates Mypt1 in epithelial organisation.

A genetic model of congenital intestinal atresia implicates Mypt1 in epithelial organisation.

Journal: Disease models & mechanisms

Published: August 19, 2025

Identification of a Risk Allele at SLC41A3 and a Protective Allele HLA-DPB1*02:01 Associated with Sarcopenia in Japanese.

Identification of a Risk Allele at SLC41A3 and a Protective Allele HLA-DPB1*02:01 Associated with Sarcopenia in Japanese.

Journal: Gerontology

Published: December 27, 2024

Peripheral blood GATA2 expression impacts RNF213 mutation penetrance and clinical severity in moyamoya disease.

Peripheral blood GATA2 expression impacts RNF213 mutation penetrance and clinical severity in moyamoya disease.

Journal: Stroke and vascular neurology

Published: May 28, 2024

Whole-genome sequencing to identify rare variants in East Asian patients with dementia with Lewy bodies.

Whole-genome sequencing to identify rare variants in East Asian patients with dementia with Lewy bodies.

Journal: npj aging

Published: May 27, 2024

Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype.

Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype.

Journal: Frontiers in genetics

Published: February 07, 2024

CRISPR/Cas9-mediated knock-in cells of the late-onset Alzheimer's disease-risk variant, SHARPIN G186R, reveal reduced NF-κB pathway and accelerated Aβ secretion.

CRISPR/Cas9-mediated knock-in cells of the late-onset Alzheimer's disease-risk variant, SHARPIN G186R, reveal reduced NF-κB pathway and accelerated Aβ secretion.

Journal: Journal of human genetics

Published: October 10, 2023

A gene regulatory network combining Pax3/7, Sox10 and Mitf generates diverse pigment cell types in medaka and zebrafish.

A gene regulatory network combining Pax3/7, Sox10 and Mitf generates diverse pigment cell types in medaka and zebrafish.

Journal: Development (Cambridge, England)

Published: June 23, 2023

Angiogenic and inflammatory responses in human induced microglia-like (iMG) cells from patients with Moyamoya disease.

Angiogenic and inflammatory responses in human induced microglia-like (iMG) cells from patients with Moyamoya disease.

Journal: Scientific reports

Published: June 16, 2023

De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.

De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.

Journal: Human molecular genetics

Published: June 01, 2021

pnp4a Is the Causal Gene of the Medaka Iridophore Mutant guanineless.

pnp4a Is the Causal Gene of the Medaka Iridophore Mutant guanineless.

Journal: G3 (Bethesda, Md.)

Published: March 05, 2017

Showing 1-12 of 22

Last Updated: 09/26/2026