Notch signaling pathway modulation by food functional ingredients: mechanisms, cancer and immunoregulation. [PDF]
Nie RZ +11 more
europepmc +1 more source
Whole‐exome sequencing of five families with non‐medullary thyroid cancer revealed three candidate genes. Functional analyses confirmed BCL2L11 as a strong candidate gene for hereditary predisposition to non‐medullary thyroid cancer. ABSTRACT Familial non‐medullary thyroid cancer, defined as two or more affected first‐degree relatives, accounts for 3 ...
Duygu Abbasoglu +9 more
wiley +1 more source
Mechanistic study of HIF-1α-mediated regulation of the Notch1 pathway in promoting radioresistance in head and neck squamous cell carcinoma: a comprehensive analysis based on bioinformatics and functional experiments. [PDF]
Bao R, Liao J.
europepmc +1 more source
Novel NOTCH3 alteration expanding the molecular spectrum of pericytic tumours: report of two cases
Introduction Myofibromas are part of the pericytic tumour family, which includes myopericytomas, glomus tumours and angioleiomyomas. While they typically display benign behaviour when arising in the skin and subcutaneous tissues of the head and neck, rare aggressive variants have been reported, particularly those with visceral or intracranial ...
Irena Antonia Ungureanu +7 more
wiley +1 more source
Genotype-to-phenotype mapping of somatic clonal mosaicism via single-cell co-capture of DNA mutations and mRNA transcripts. [PDF]
Yuan DJ +19 more
europepmc +1 more source
RB1 inactivation in cutaneous carcinomas
Among skin carcinomas, recurrent RB1 inactivation is observed in Merkel cell carcinoma, in a subset of squamous cell carcinoma with bowenoid morphology, in sebaceous carcinoma and in the recently described Wnt/beta‐catenin rosette‐forming carcinoma.
Tiffany Liv +8 more
wiley +1 more source
FoxO1, together with Notch1, promotes microglial activation to induce pathological changes in the retinal vasculature under hypoxia. [PDF]
Wu X +7 more
europepmc +1 more source
Clinical, genetic, and familial features of POT1 tumor predisposition syndrome
Abstract Background Protection of telomere 1 (POT1) tumor predisposition syndrome (POT1‐TPD) is a hereditary leukemia syndrome that is identified in ∼5% of patients with chronic lymphocytic leukemia (CLL) and is characterized by a predisposition to other cancers, including gliomas, melanomas, and angiosarcomas.
Courtney D. DiNardo +13 more
wiley +1 more source
YTHDF1 targets the chemotherapy response by suppressing NOTCH1-induced stemness in colorectal cancer. [PDF]
Cheung H +16 more
europepmc +1 more source
The role of cytokines in ovarian cancer drug resistance
Abstract Ovarian cancer is the leading cause of death among women diagnosed with female reproductive system cancers. While significant advances have been made in treating various types of cancer, progress in ovarian cancer treatment over the past 20 years has been minimal, and the treatment course of ovarian cancer is not linear. Although many patients
Lu Wang +7 more
wiley +1 more source

