Tae-ik Choi

Daejeon, Republic of Korea

Last Updated: 09/26/2026

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Found 34 publications

A Dosage-Dependent Dominant-Negative Mechanism of SLC45A2(W74R) in Autosomal Dominant Oculocutaneous Albinism Revealed by Zebrafish Modeling.

A Dosage-Dependent Dominant-Negative Mechanism of SLC45A2(W74R) in Autosomal Dominant Oculocutaneous Albinism Revealed by Zebrafish Modeling.

Journal: Translational vision science & technology

Published: February 18, 2026

Preserving spatial and quantitative information in unpaired biomedical image-to-image translation.

Preserving spatial and quantitative information in unpaired biomedical image-to-image translation.

Journal: Cell reports methods

Published: October 18, 2024

VprBP regulates osteoclast differentiation via an epigenetic mechanism involving histone H2A phosphorylation.

VprBP regulates osteoclast differentiation via an epigenetic mechanism involving histone H2A phosphorylation.

Journal: Epigenetics & chromatin

Published: September 11, 2024

RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish model.

RFC2 may contribute to the pathogenicity of Williams syndrome revealed in a zebrafish model.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: May 30, 2024

A Novel Anticancer Peptide Derived from Bryopsis plumosa Regulates Proliferation and Invasion in Non-Small Cell Lung Cancer Cells.

A Novel Anticancer Peptide Derived from Bryopsis plumosa Regulates Proliferation and Invasion in Non-Small Cell Lung Cancer Cells.

Journal: Marine drugs

Published: October 13, 2023

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt.

Journal: American journal of human genetics

Published: August 06, 2023

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).

Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3).

Journal: Human mutation

Published: July 14, 2023

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

Journal: Annals of neurology

Published: May 30, 2023

Impairments of cerebellar structure and function in a zebrafish KO of neuropsychiatric risk gene znf536.

Impairments of cerebellar structure and function in a zebrafish KO of neuropsychiatric risk gene znf536.

Journal: Translational psychiatry

Published: April 26, 2023

IFT46 gene promoter-driven ciliopathy disease model in zebrafish.

IFT46 gene promoter-driven ciliopathy disease model in zebrafish.

Journal: Frontiers in cell and developmental biology

Published: April 05, 2023

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Journal: Research square

Published: March 30, 2023

Expanding allelic and phenotypic spectrum of ZC4H2-related disorder: A novel hypomorphic variant and high prevalence of tethered cord.

Expanding allelic and phenotypic spectrum of ZC4H2-related disorder: A novel hypomorphic variant and high prevalence of tethered cord.

Journal: Clinical genetics

Published: July 01, 2022

Showing 1-12 of 34

Last Updated: 09/26/2026