Daisuke Iejima

Tokyo, Japan

Last Updated: 09/26/2026

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Found 13 publications

Clinical features and molecular mechanisms of RP1L1 variants causing occult macular dystrophy.

Clinical features and molecular mechanisms of RP1L1 variants causing occult macular dystrophy.

Journal: HGG advances

Published: November 08, 2024

The membrane-linked adaptor FRS2β fashions a cytokine-rich inflammatory microenvironment that promotes breast cancer carcinogenesis.

The membrane-linked adaptor FRS2β fashions a cytokine-rich inflammatory microenvironment that promotes breast cancer carcinogenesis.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 19, 2021

METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma.

METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma.

Journal: The Journal of clinical investigation

Published: August 06, 2021

Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro.

Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro.

Journal: The Journal of biological chemistry

Published: November 13, 2020

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis.

Journal: Human genome variation

Published: August 13, 2018

Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses.

Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: July 26, 2018

Effect of Timolol on Optineurin Aggregation in Transformed Induced Pluripotent Stem Cells Derived From Patient With Familial Glaucoma.

Effect of Timolol on Optineurin Aggregation in Transformed Induced Pluripotent Stem Cells Derived From Patient With Familial Glaucoma.

Journal: Investigative ophthalmology & visual science

Published: May 31, 2018

Significance of optineurin mutations in glaucoma and other diseases.

Significance of optineurin mutations in glaucoma and other diseases.

Journal: Progress in retinal and eye research

Published: March 28, 2016

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability.

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability.

Journal: Scientific reports

Published: March 17, 2016

HTRA1 Overexpression Induces the Exudative Form of Age-related Macular Degeneration.

HTRA1 Overexpression Induces the Exudative Form of Age-related Macular Degeneration.

Journal: Journal of stem cells

Published: January 01, 2015

HTRA1 (high temperature requirement A serine peptidase 1) gene is transcriptionally regulated by insertion/deletion nucleotides located at the 3' end of the ARMS2 (age-related maculopathy susceptibility 2) gene in patients with age-related macular degeneration.

HTRA1 (high temperature requirement A serine peptidase 1) gene is transcriptionally regulated by insertion/deletion nucleotides located at the 3' end of the ARMS2 (age-related maculopathy susceptibility 2) gene in patients with age-related macular degeneration.

Journal: The Journal of biological chemistry

Published: December 19, 2014

Overexpression of HtrA1 and exposure to mainstream cigarette smoke leads to choroidal neovascularization and subretinal deposits in aged mice.

Overexpression of HtrA1 and exposure to mainstream cigarette smoke leads to choroidal neovascularization and subretinal deposits in aged mice.

Journal: Investigative ophthalmology & visual science

Published: September 11, 2014

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Last Updated: 09/26/2026