Yeming Yang

The Sichuan Provincial Key Laboratory For Genetic Diseases And Center For Medical Genetics
Chengdu, 610072, China

Last Updated: 09/26/2026

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Found 44 publications

WTAP mediated m6A methylation modulates retinal photoreceptor function via facilitating of REEP6, PDE6B and RDH12 translation.

WTAP mediated m6A methylation modulates retinal photoreceptor function via facilitating of REEP6, PDE6B and RDH12 translation.

Journal: Science China. Life sciences

Published: November 04, 2025

Unveiling ZNF124 as a novel determinant in neurodegeneration: orchestration of photoreceptor homeostasis through MSX2 transcriptional regulation.

Unveiling ZNF124 as a novel determinant in neurodegeneration: orchestration of photoreceptor homeostasis through MSX2 transcriptional regulation.

Journal: Cell death & disease

Published: July 10, 2025

Mettl3-Mediated m6A Modification is Essential for Visual Function and Retinal Photoreceptor Survival.

Mettl3-Mediated m6A Modification is Essential for Visual Function and Retinal Photoreceptor Survival.

Journal: Investigative ophthalmology & visual science

Published: December 27, 2024

Deletion of Transmembrane protein 184b leads to retina degeneration in mice.

Deletion of Transmembrane protein 184b leads to retina degeneration in mice.

Journal: Cell proliferation

Published: June 02, 2024

The m6A reader YTHDC2 maintains visual function and retinal photoreceptor survival through modulating translation of PPEF2 and PDE6B.

The m6A reader YTHDC2 maintains visual function and retinal photoreceptor survival through modulating translation of PPEF2 and PDE6B.

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

Published: August 30, 2023

Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice.

Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice.

Journal: The FEBS journal

Published: February 07, 2023

The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival.

The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival.

Journal: Genes & diseases

Published: September 21, 2022

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy.

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy.

Journal: Genes & diseases

Published: April 27, 2022

CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis.

CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis.

Journal: JCI insight

Published: January 12, 2022

Loss of Wtap results in cerebellar ataxia and degeneration of Purkinje cells.

Loss of Wtap results in cerebellar ataxia and degeneration of Purkinje cells.

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

Published: December 06, 2021

Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival.

Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival.

Journal: BMC biology

Published: November 25, 2021

Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration.

Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration.

Journal: Journal of cellular physiology

Published: October 17, 2021

Showing 1-12 of 44

Last Updated: 09/26/2026