Results 81 to 90 of about 2,529,505 (194)
Perivascular matrix densification promotes the emergence of aberrant endothelial tip cells (ATECs) that invade and persist within fibrotic microenvironments. Using in vivo lineage tracing and a human microvessel model, this study shows that fibrous matrix cues destabilize VE‐cadherin–mediated junctions to gate TGF‐β signaling, inducing a pro ...
Jingyi Xia +17 more
wiley +1 more source
Information of primers used in PCR amplification for NOTCH3 gene.
Information of primers used in PCR amplification for NOTCH3 gene.
Le Bo (609957) +7 more
core +1 more source
Integrative single‐cell and bulk transcriptomic analyses identified a highly inflammatory macrophage state and a vascular smooth muscle cell (VSMC) remodeling continuum in human atherosclerotic plaques. Candidate ligand‐receptor and ligand‐associated target gene expression patterns linked inflammatory macrophage activation with osteogenic/modulated ...
Xinyu Dong +8 more
wiley +1 more source
目的 对4例NOTCH3基因突变的遗传性脑小血管病患者的临床及认知特点进行分析比较。 方法 回顾性收集2015年5月-2017年9月天津市环湖医院神经内科收治的4例NOTCH3基因突变的遗 传性脑小血管病患者的临床资料,分析其首发症状、临床表现、影像学检查、辅助检查、基因检测及 相关神经心理学评估等方面的特点。 结果 4例NOTCH3基因突变的患者中2例以急性缺血性卒中,1例以认知功能障碍,1例以头晕头痛就 诊,其中1例患者除了有急性卒中症状外还伴有家族性秃头和腰痛。4例患者中2例伴有脑血管病危险 因素。
陈嫄, 周玉颖, 王艳, 张惠红
doaj +1 more source
Migraine: Epidemiology, Risk Factors, Pathophysiology, and Treatment
Migraine is a highly prevalent, female‐predominant, and disabling brain disorder shaped by genetic susceptibility, hormonal influences, modifiable attack factors, and comorbidity‐related progression. This review integrates current evidence on migraine epidemiology, phase‐specific neurovascular and neuroglial mechanisms, including CGRP signaling and ...
Weiwei Lu +9 more
wiley +1 more source
RANBP1 Regulates NOTCH3-Mediated Autophagy in High Glucose-Induced Vascular Smooth Muscle Cells
Background: Vascular smooth muscle cells(VSMCs) phenotypic switching under hyperglycemic conditions accelerates atherosclerotic progression.
Zhong-jiao Xu +11 more
doaj +1 more source
R54C Mutation of NOTCH3 Gene in the First Rungus Family with CADASIL
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary stroke caused by mutations in NOTCH3 gene. We report the first case of CADASIL in an indigenous Rungus (Kadazan-Dusun) family in Kudat, Sabah, Malaysia confirmed by a R54C (c.160C>T, p.Arg54Cys) mutation in the NOTCH3. This mutation
Lim, Kheng Seang +10 more
openaire +5 more sources
Traditional Chinese Medicine for lung cancer: Mechanisms, clinical evidence, and future perspectives
Graphical abstract represents the risk factors for lung cancer, TCM efficacy and clinical outcomes to future challenges. Abstract Lung cancer remains a leading cause of global cancer mortality. Despite advances in conventional treatments such as surgery, chemotherapy, targeted therapy, and immunotherapy, challenges including drug resistance, toxicity ...
Zhangdeng Chen, Liujun Bao
wiley +1 more source
ObjectivesFibroleukin (FGA) and NOTCH3 are vital in both exercise-induced muscle adaptation and colon adenocarcinoma (COAD) progression. This study aims to elucidate the roles of FGA and NOTCH3 in phenotypic variations of striated muscle induced by ...
Hongbiao Luo +8 more
doaj +1 more source
ABSTRACT Sheep production contributes to a secure and diverse food and fibre supply in the United States, with growing ethnic diversity strengthening demand. Katahdin is a composite hair‐type sheep breed developed in the United States that has become the most popular breed in many regions of the country and the first one to have genomic selection ...
Alejandra Toro Ospina +6 more
wiley +1 more source

