[HTML][HTML] Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative …
Endoplasmic reticulum (ER) membrane protein complex (EMC) is required for the co-
translational insertion of newly synthesized multi-transmembrane proteins. Compromised …
translational insertion of newly synthesized multi-transmembrane proteins. Compromised …
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
W Liu, S Li, M Yang, J Ma, L Liu, P Fei, Q Xiang… - Elife, 2024 - elifesciences.org
Familial exudative vitreoretinopathy (FEVR) is a severe genetic disorder characterized by
incomplete vascularization of the peripheral retina and associated symptoms that can lead …
incomplete vascularization of the peripheral retina and associated symptoms that can lead …
Long non-coding RNA in coronary artery disease: the role of PDXDC1-AS1 and SFI1-AS1
S He, S Zhang, YJ Wang, XK Gan, JX Chen… - Functional & Integrative …, 2023 - Springer
This study investigates the interaction between long non-coding RNAs (lncRNAs) and
metabolic risk factors that contribute to coronary artery disease (CAD). A total transcriptome …
metabolic risk factors that contribute to coronary artery disease (CAD). A total transcriptome …
Transcriptional data analysis reveals the association between infantile hemangiomas and venous malformations
B Huang, P Zhang, YY Zhong, K Wang, XM Chen… - Frontiers in …, 2022 - frontiersin.org
Background: Infantile hemangiomas (IH) and venous malformations (VM) are the most
common types of vascular abnormalities that seriously affect the health of children. Although …
common types of vascular abnormalities that seriously affect the health of children. Although …
Defective CAPSL function causes impaired retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy
W Liu, S Li, M Yang, J Ma, L Liu, P Fei, Q Xiang… - medRxiv, 2024 - medrxiv.org
Familial exudative vitreoretinopathy (FEVR) is a severe genetic disorder characterized by
incomplete vascularization of the peripheral retina and associated symptoms that can lead …
incomplete vascularization of the peripheral retina and associated symptoms that can lead …
[PDF][PDF] Defective EMC1 drives abnormal retinal angiogenesis via Wnt/b-catenin signaling and may be associated with the pathogenesis of familial exudative …
Endoplasmic reticulum (ER) membrane protein complex (EMC) is required for the
cotranslational insertion of newly synthesized multi-transmembrane proteins. Compromised …
cotranslational insertion of newly synthesized multi-transmembrane proteins. Compromised …
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene loci
Background: Chronic hyperglycemia is a major risk factor for glomerular or retinal
microangiopathy and cardiovascular complications of type 1 diabetes (T1D). At the interface …
microangiopathy and cardiovascular complications of type 1 diabetes (T1D). At the interface …
First person–Wenjing Liu
W Liu - Journal of Cell Science, 2022 - journals.biologists.com
First Person is a series of interviews with the first authors of a selection of papers published
in Journal of Cell Science, helping early-career researchers promote themselves alongside …
in Journal of Cell Science, helping early-career researchers promote themselves alongside …