Results 111 to 120 of about 2,529,587 (194)
Phenotypic variability in 446 CADASIL patients: Impact of NOTCH3 gene mutation location in addition to the effects of age, sex and vascular risk factors. [PDF]
Dupé C +11 more
europepmc +1 more source
The epigenetic factor CTCF-L/BORIS regulates the NOTCH3 gene transcription in cancer cells
Aberrant up-regulation of NOTCH3 gene plays a critical role in cancer pathogenesis. However, the underlying mechanisms are still unknown. We tested here the hypothesis that aberrant epigenetic modifications in the NOTCH3 promoter region might account for
SCREPANTI, Isabella +5 more
core
The Notch family is a highly conserved gene group that regulates cell-cell interaction, embryogenesis, and tissue commitment. This review article focuses on the third Notch family subtype, Notch3.
Jason Whitt +5 more
core +1 more source
Purpose Notch signaling dysregulation is implicated in the development of pancreatic adenocarcinoma (PDAC). Tarextumab is a fully human IgG2 antibody that inhibits Notch2/3 receptors.
Zishuo Ian Hu +21 more
doaj +1 more source
Background CADASIL(Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)is an inherited small vessel disease caused by mutations in NOTCH3 gene.
Weili Liu +6 more
doaj +1 more source
A NOTCH3 transcriptional module induces cell motility in neuroblastoma
Neuroblastoma is a childhood tumor of the peripheral sympathetic nervous system with an often lethal outcome due to metastatic disease. Migration and epithelial-mesenchymal transitions have been implicated in metastasis but they are hardly investigated ...
van Sluis, Peter +5 more
core +1 more source
Colon stem cell characterization in normal and tumoral tissues: description of a novel feed-forward circuit of Msi-1 regulation [PDF]
Normal tissues are organized in a hierarchical fashion, where rare somatic cells endowed with stem-like properties give origin to a population of differentiated cells forming the bulk of tissue.
Pastò, Anna
core
Correlation Analysis of Rare NOTCH3 Gene Variants and Macrovascular Lesions
ObjectiveCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoen-cephalopathy (CADASIL) is caused by NOTCH3 gene variants and is predominantly characterized by cerebral small vessel disease.
WANG You +3 more
doaj +1 more source
Objective: The aim of the present study was to analyse the coding region and intron-exon boundaries of the NOTCH3 gene in a large cohort of patients af- fected by leukoencephalopathy to investigate the presence of genetic vari- ants. Patients and methods:
M Muglia +10 more
core
Notch3 is essential for regulation of the renal vascular tone
—The Notch3 receptor participates in the development and maturation of vessels. Mutations of Notch3 in humans are associated with defective regulation of cerebral blood flow.
Nada Boulos +11 more
core +1 more source

