Results 81 to 90 of about 1,858 (192)
Frontiers in Neurology, 2018 Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder characterized by the presence of renal cysts and specific extrarenal abnormalities.
Christian Thomas +7 more
doaj +1 more source
Advanced Science, Volume 12, Issue 10, March 13, 2025.Imaging fast luminescence kinetics has required costly camera setups. The RIOM and HIOM protocols relying on modulated illumination are introduced to make this possible with standard low‐cost cameras, even under ambient light. These are implemented to measure the photoactivation time of a reversibly photoswitchable protein and microsensors and recover ...
Hélène Merceron +5 more
wiley +1 more source
, 2014 Sequencing of exon 5 (reverse strand, CCM1) of CV126 index patient showing mutation c.618_619delinsG.
Francisca Solano (513838) +9 more
core +1 more source
Transfer morphological features for segmentation with few labels on fluorescent mitochondria images
IET Image Processing, Volume 19, Issue 1, January/December 2025.Deep learning‐based approaches have demonstrated promising performance; however, the scarcity of labeled mitochondrial data presents a significant challenge. To address this, we propose a high‐precision segmentation framework leveraging inductive transfer learning.
Tianyi Zhang +5 more
wiley +1 more source
A novel CCM2 gene mutation associated with family cerebral cavernous malformation
Frontiers in Aging Neuroscience, 2016 Background: Cerebral cavernous malformations (CCMs) are common vascular malformations that predominantly arise in the central nervous system and are mainly characterized by enlarged vascular cavities without intervening brain parenchyma.
Wen-Qing Huang +16 more
doaj +1 more source
Ccm3 functions in a manner distinct from Ccm1 and Ccm2 in a zebrafish model of CCM vascular disease
, 2012 Cerebral cavernous malformations (CCMs) are vascular anomalies of the central nervous system that arise due to mutations in genes encoding three unrelated proteins: CCM1 (KRIT1); CCM2 (Malcavernin/OSM) and CCM3 (PDCD10).
Ian C. Scott +7 more
core +1 more source
, 2021 Enhanced Yes-associated protein (YAP)/transcriptional co-activator with PDZ-binding motif (TAZ) signaling is correlated with the extraprostatic extension of prostate cancer. However, the mechanism by which YAP/TAZ signaling becomes hyperactive and drives
Jaehong Kim +6 more
core +1 more source
Comparative omics of CCM signaling complex (CSC)
Chinese Neurosurgical Journal, 2020 Background Cerebral cavernous malformations (CCMs), a major neurosurgical condition, characterized by abnormally dilated intracranial capillaries, result in increased susceptibility to stroke.
Johnathan Abou-Fadel +3 more
doaj +1 more source
Fare meme kanseri modeli primer tümör ve metastazlarında CCM1, CCM2, CCM3 ekspresyonlarının değerlendirilmesi [PDF]
, 2017 Amaç: CCM1, CCM2 ve CCM3 genlerinde tanımlanan mutasyonlar sporadik ya da kalıtsal olup santral sinir sisteminde görülen serebral kavernoz malformasyonların (SKM) sebebidir.
Cici, Mansur
core
Interrogating the ccm-3 Gene Network
Cell Reports, 2018 Summary: Cerebral cavernous malformations (CCMs) are neurovascular lesions caused by mutations in one of three genes (CCM1–3). Loss of CCM3 causes the poorest prognosis, and little is known about how it regulates vascular integrity. The C.
Benjamin Lant +9 more
doaj +1 more source