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Profil bibliographique

Rui Chen

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

404Publications signalées
19607Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Retinal Development and DisordersRetinal Diseases and TreatmentsSingle-cell and spatial transcriptomicsGenomics and Rare DiseasesCRISPR and Genetic Engineering

Les publications récentes

Accès ouvert 2026 article OpenAlex

Segmented poly(A) tails with microRNA target sites confer tissue-specific regulation for mRNA therapeutics

Rui Qian Qi, Rui Chen, Hua Chen, Hui Bao et autres

Abstract Targeted delivery and controlled expression of mRNA-LNPs are critical for the development of safe and effective mRNA medicines. However, efficient post-delivery regulation of mRNA-LNP expression remains challenging. In this study, we engineered segmented poly(A) tail variants that function as gene-specific regulatory …

cn (code pays fourni par la source)

0 citations Molecular Therapy — Nucleic Acids
Accès ouvert 2026 preprint OpenAlex

An Integrated muti-omics cell atlas of the human trabecular meshwork and ciliary body

Jinjing Jian, Xuan Bao, Yi-Xiang Wang, Y Zheng et autres

Abstract The trabecular meshwork (TM) and ciliary body (CB) regulate aqueous humor dynamics and intraocular pressure (IOP), and TM/Schlemm’s canal (SC) dysfunction underlies glaucoma. Here, we present a spatially resolved multi-omics atlas of human TM and CB, integrating snRNA-seq, scRNA-seq, and snATAC-seq …

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0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2026 article OpenAlex

Bi-allelic variants in AP5Z1 and AP5B1 lead to retinal degeneration

Hafiz Muhammad Jafar Hussain, Meng Wang, Paul Yang, Behnoosh Tasharrofi et autres

Inherited retinal diseases (IRDs) comprise a diverse group of disorders that frequently lead to progressive vision impairment and blindness. Despite advances in genetic testing, a significant number of IRD cases remain genetically unsolved, often due to unidentified disease-associated genes or variants. This …

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1 citation Human Genetics and Genomics Advances
Accès ouvert 2025 article OpenAlex

Retinol tracing within murine neural retina reveals cell type–specific retinol transport and distribution

Zachary J Engfer, Grażyna Palczewska, Samuel W. Du, Jianye Zhang et autres

11-cis-Retinal is essential for light perception in mammalian photoreceptors (PRs), and aberrations in retinoid transformations cause severe retinal diseases. Understanding these processes is crucial for combating blinding diseases. The visual cycle, operating within PRs and the retinal pigment epithelium (RPE), regenerates 11-cis-retinal …

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3 citations Journal of Clinical Investigation
Accès ouvert 2025 article OpenAlex

Rapamycin and Suramin Effects on TNF‐⍺‐Mediated Mast Cell and Brain Microvascular Endothelial Cell Dysfunction

Katherine A. Ebbert, Rui Chen, Robert A. Culibrk, Daniel J. Yeisley et autres

Chronic blood-brain barrier (BBB) disruption due to impaired function of brain microvascular endothelial cells (BMECs) is commonly observed in neuroinflammatory and neurodegenerative conditions. Current treatment approaches are generally limited in their capacity to reduce this dysfunction, with the Akt/mTOR/GSK pathway modulator rapamycin …

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1 citation Biotechnology and Bioengineering
Accès ouvert 2025 article OpenAlex

SFC-GS: A Multi-Objective Optimization Service Function Chain Scheduling Algorithm Based on Matching Game

Shi Kuang, Sunan Wang, Haoran Li, Siyuan Liang et autres

Service Function Chain (SFC) is a framework that dynamically orchestrates Virtual Network Functions (VNFs) and is essential to enhancing resource scheduling efficiency. However, traditional scheduling methods face several limitations, such as low matching efficiency, suboptimal resource utilization, and limited global coordination capabilities. …

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0 citations Future Internet
Accès ouvert 2025 conference-abstract OpenAlex

#ECR-Paper-05 Genome-wide insights into the genes and pathways shaping human foveal development

Ha-Jun Yoon, Alvin Lirio, Kayesha Coley, Jun Wang et autres

Background Abnormal foveal pit formation is a hallmark of foveal hypoplasia (FH), a key feature of conditions such as albinism and PAX6-related aniridia. While rare, high-penetrance variants in these disorders are well described, the broader genetic architecture of foveal development, including contributions …

gb, us, no (code pays fourni par la source)

0 citations
Accès ouvert 2025 article OpenAlex

Semi-Parametric Functional Kriging Regression Model with L1 Penalty

Rui Chen, Zhiyong Zhou

Partial functional linear models are widely studied and applied models, where the response variable is related to both general random variables and functional random variables. However, with the increasing application of data scenarios involving functional and vector-valued covariates and scalar responses in …

cn (code pays fourni par la source)

0 citations Highlights in Science Engineering and Technology
Accès ouvert 2025 article OpenAlex

Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia

Ha-Jun Yoon, Alvin Lirio, Kayesha Coley, Jun Wang et autres

Purpose: To define the genetic architecture of foveal morphology and explore its relevance to foveal hypoplasia (FH), a hallmark of developmental macular disorders. Methods: We applied deep-learning algorithms to quantify foveal pit depth from central optical coherence tomography (OCT) B-scans in 61,269 …

gb, us, no (code pays fourni par la source)

7 citations Investigative Ophthalmology & Visual Science

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