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Yeming Yang

H指数:19

被引数:1,056

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Mettl3-Mediated m A Modification is Essential for Visual Function and Retinal Photoreceptor Survival

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2024-12-270

OAAI

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

CELL PROLIFERATION

IF5.6

2024-10-070

OAAI

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

GENES & DISEASES

IF9.4

2024-03-012

OAAI

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

JOURNAL OF GENETICS AND GENOMICS

IF7.1

2024-02-011

OAAI

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

缺陷性EMC1通过Wnt/b-catenin信号驱动异常视网膜血管生成，可能与家族性渗出性玻璃体视网膜病变的发病机制有关

GENES & DISEASES

IF9.4

2023-11-0110

OAAI

Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice

IF4.2

2023-05-194

PRE

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

Wtap丢失导致小脑共济失调和浦肯野细胞变性

JOURNAL OF GENETICS AND GENOMICS

IF7.1

2022-09-0110

PRE

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

IF6.1

2022-07-2221

OA

Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathy

JOURNAL OF GENETICS AND GENOMICS

IF7.1

2022-06-0121

PRE

Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma

失调的m6A修饰促进非酒精性脂肪性肝病和肝细胞癌的脂肪生成和发展

MOLECULAR THERAPY

IF12

2022-06-0194

OA

LMBR1L regulates the proliferation and migration of endothelial cells through Norrin/β-catenin signaling

JOURNAL OF CELL SCIENCE

IF3.6

2022-03-144

OA

A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis

CELL DEATH & DISEASE

IF9.6

2021-10-297

OAAI

The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretion

MOLECULAR THERAPY

IF12

2021-09-0116

OAAI

Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis

DISEASE MODELS & MECHANISMS

IF3.3

2021-06-2510

OAAI

Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling

JOURNAL OF CLINICAL INVESTIGATION

IF13.6

2021-03-1548

OA

Identification of novel USH2A mutations in patients with autosomal recessive retinitis pigmentosa via targeted next-generation sequencing

MOLECULAR MEDICINE REPORTS

IF3.5

2020-04-226

OAAI

Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice

HUMAN MOLECULAR GENETICS

IF3.2

2020-04-0218

PREAI

Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy

GENETICS IN MEDICINE

IF6.2

2020-01-0143

OAAI

ER complex proteins are required for rhodopsin biosynthesis and photoreceptor survival in Drosophila and mice

CELL DEATH AND DIFFERENTIATION

IF15.4

2019-07-0132

OAAI

TMEM30A deficiency n endothelial cells impairs cell proliferation and angiogenesis

JOURNAL OF CELL SCIENCE

IF3.6

2019-04-0317

OAAI