Search Results - "Yang, Yeming"
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Tmem30a deficiency leads to retinal rod bipolar cell degeneration
Published in Journal of neurochemistry (01-02-2019)“…Phospholipids are asymmetrically distributed across the mammalian plasma membrane, with phosphatidylserine (PS) and phosphatidylethanolamine concentrated in…”
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Loss of the ER membrane protein complex subunit Emc3 leads to retinal bipolar cell degeneration in aged mice
Published in PloS one (04-09-2020)“…The endoplasmic reticulum (ER) membrane protein complex (EMC) is a conserved protein complex involved in inserting the transmembrane domain of membrane…”
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TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis
Published in Journal of cell science (01-04-2019)“…Phosphatidylserine (PS) asymmetry in the eukaryotic cell membrane is maintained by a group of proteins belonging to the P4-ATPase family, namely, PS flippases…”
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Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice
Published in Human molecular genetics (27-06-2020)“…Abstract Variants in interphotoreceptor matrix proteoglycans (IMPG2) have been reported in retinitis pigmentosa (RP) and vitelliform macular dystrophy (VMD)…”
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Three-Party Password Authentication and Key Exchange Protocol Based on MLWE
Published in Symmetry (Basel) (01-09-2023)“…With the rapid development of quantum theory, the discrete logarithm problem and significant integer factorization problem have polynomial solution algorithms…”
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Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival
Published in BMC biology (13-06-2022)“…As the most abundant epigenetic modification of eukaryotic mRNA, N6-methyladenosine (m6A) modification has been shown to play a role in mammalian nervous…”
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Tmem30a Plays Critical Roles in Ensuring the Survival of Hematopoietic Cells and Leukemia Cells in Mice
Published in The American journal of pathology (01-06-2018)“…The fundamental structure of eukaryotic cell plasma membrane is the phospholipid bilayer, which contains four major phospholipids. These phospholipids are…”
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Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis
Published in Disease models & mechanisms (01-06-2021)“…The asymmetric distribution of phosphatidylserine (PS) in the cytoplasmic leaflet of eukaryotic cell plasma membranes is regulated by a group of P4-ATPases…”
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Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters
Published in The American journal of pathology (01-12-2017)“…Mutations in ATP8B1 or ATP11C (members of P4-type ATPases) cause progressive familial intrahepatic cholestasis type 1 in human or intrahepatic cholestasis in…”
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A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Published in Cell death & disease (29-10-2021)“…Glaucoma is a leading cause of blindness, affecting 70 million people worldwide. Owing to the similarity in anatomy and physiology between human and mouse eyes…”
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The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival
Published in Genes & diseases (01-03-2024)“…The endoplasmic reticulum (ER) membrane protein complex (EMC) is responsible for monitoring the biogenesis and synthetic quality of membrane proteins with…”
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Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells
Published in Cell death & disease (05-09-2018)“…Phospholipids are asymmetrically distributed across mammalian plasma membrane with phosphatidylserine (PS) and phosphatidylethanolamine concentrated in the…”
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Loss of Tmem30a leads to photoreceptor degeneration
Published in Scientific reports (24-08-2017)“…Phosphatidylserine (PS) is asymmetrically distributed between the outer and inner leaflets of the plasma membrane in eukaryotic cells. PS asymmetry on the…”
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Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy
Published in Genes & diseases (01-11-2023)“…Endoplasmic reticulum (ER) membrane protein complex (EMC) is required for the co-translational insertion of newly synthesized multi-transmembrane proteins…”
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CTNND1 variants cause familial exudative vitreoretinopathy through Wnt/Cadherin axis
Published in JCI insight (22-07-2022)“…Familial exudative vitreoretinopathy (FEVR) is a hereditary disorder that can cause vision loss. The CTNND1 gene encodes a cellular adhesion protein…”
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Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice
Published in Frontiers in cell and developmental biology (18-01-2022)“…The asparaginase and isoaspartyl peptidase 1 (ASRGL1) is an L-asparaginase and beta-aspartyl peptidase enzyme that may be involved in the formation of…”
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Dialect competence, dialect attitude and social inclusion: A case study of migrants in Chongqing, China
Published in International multilingual research journal (02-10-2023)“…Adopting methods of the questionnaire, matched-guise test and semi-structured interview among different occupational groups of migrants in Chongqing, China,…”
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Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma
Published in Molecular therapy (01-06-2022)“…Type 2 diabetes mellitus (DM2) is associated closely with non-alcoholic fatty liver disease (NAFLD) by affecting lipid metabolism, which may lead to…”
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The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretion
Published in Molecular therapy (01-09-2021)“…The processing, maturation, and secretion of insulin are under precise regulation, and dysregulation causes profound defects in glucose handling, leading to…”
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Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration
Published in Journal of cellular physiology (01-06-2022)“…Yes‐associated protein (YAP) is a major component of the Hippo pathway involved in development, growth, repair and homeostasis. Nonsense YAP1 mutations in…”
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