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Tmem30a deficiency leads to retinal rod bipolar cell degeneration

Journal of neurochemistry, 2019-02, Vol.148 (3), p.400-412

2019

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

Cell death & disease, 2021-10, Vol.12 (11), p.1017-1017, Article 1017

2021

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

Human molecular genetics, 2020-06, Vol.29 (10), p.1624-1634

2020

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

BMC biology, 2022-06, Vol.20 (1), p.140-140, Article 140

2022

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TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis

Journal of cell science, 2019-04, Vol.132 (7)

2019

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

Disease models & mechanisms, 2021-06, Vol.14 (6)

2021

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The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis

Science China. Life sciences, 2021-11, Vol.64 (11), p.1868-1883

2021

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

Genes & diseases, 2024-03, Vol.11 (2), p.1035-1049

2024

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Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells

Cell death & disease, 2018-09, Vol.9 (9), p.899-13, Article 899

2018

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Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice

Frontiers in cell and developmental biology, 2022-01, Vol.9, p.783547-783547

2022

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

Molecular therapy, 2022-06, Vol.30 (6), p.2342-2353

2022

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

Molecular therapy, 2021-09, Vol.29 (9), p.2854-2872

2021

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

Journal of cellular physiology, 2022-06, Vol.237 (6), p.2673-2689

2022

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

Journal of cell science, 2022-03, Vol.135 (6)

2022

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Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice

The FEBS journal, 2023-09, Vol.290 (17), p.4356-4370

2023

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

Cell proliferation, 2024-10, p.e13751

2024

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

Journal of genetics and genomics, 2022-09, Vol.49 (9), p.847-858

2022

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

Journal of genetics and genomics, 2024-02, Vol.51 (2), p.208-221

2024

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The m 6 A reader YTHDC2 maintains visual function and retinal photoreceptor survival through modulating translation of PPEF2 and PDE6B

Journal of genetics and genomics, 2024-02, Vol.51 (2), p.208

2024

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Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A

BioMed research international, 2020, Vol.2020 (2020), p.1-9

2020

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

Journal of genetics and genomics, 2022-06, Vol.49 (6), p.590-594

2022

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Identification of Novel Mutations in the FZD4 and NDP Genes in Patients with Familial Exudative Vitreoretinopathy in South India

Genetic testing and molecular biomarkers, 2020-02, Vol.24 (2), p.92-98

2020

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

Molecular medicine reports, 2020-07, Vol.22 (1), p.193-200

2020

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Identification of Novel EYS Mutations by Targeted Sequencing Analysis

Genetic testing and molecular biomarkers, 2020-11, Vol.24 (11), p.745-753

2020

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Targeted Next Generation Sequencing Revealed Novel PRPF31 Mutations in Autosomal Dominant Retinitis Pigmentosa

Genetic testing and molecular biomarkers, 2018-07, Vol.22 (7), p.425-432

2018

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Tmem30a deficiency leads to retinal rod bipolar cell degeneration

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

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

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

TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis

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

The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis

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

Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells

Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice

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

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

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

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

Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice

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

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

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

The m 6 A reader YTHDC2 maintains visual function and retinal photoreceptor survival through modulating translation of PPEF2 and PDE6B

Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A

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

Identification of Novel Mutations in the FZD4 and NDP Genes in Patients with Familial Exudative Vitreoretinopathy in South India

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

Identification of Novel EYS Mutations by Targeted Sequencing Analysis

Targeted Next Generation Sequencing Revealed Novel PRPF31 Mutations in Autosomal Dominant Retinitis Pigmentosa

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