Results 31 to 40 of about 20,241 (230)

Acquisition of NFKB1-selective DNA binding by substitution of four amino acid residues from NFKB1 into RelA. [PDF]

open access: yesMolecular and Cellular Biology, 1993
The subunits of NF-kappa B, NFKB1 (formerly p50) and RelA (formerly p65), belong to a growing family of transcription factors that share extensive similarity to the c-rel proto-oncogene product. The homology extends over a highly conserved stretch of approximately 300 amino acids termed the Rel homology domain (RHD).
Steven M. Ruben   +4 more
openaire   +3 more sources

c‐Rel–dependent Chk2 signaling regulates the DNA damage response limiting hepatocarcinogenesis

open access: yesHepatology, EarlyView., 2022
In response to genotoxic injury, c‐Rel upregulates ATM‐Chk2‐p53 pathway DNA damage proteins to limiting hepatocarcinogenesis. Abstract Background and Aims Hepatocellular carcinoma (HCC) is a leading cause of cancer‐related death. The NF‐κB transcription factor family subunit c‐Rel is typically protumorigenic; however, it has recently been reported as a
Jack Leslie   +17 more
wiley   +1 more source

A novel NFkB1 mutation linking pyoderma gangrenosum and common variable immunodeficiency [PDF]

open access: yesJAAD Case Reports, 2021
Pyoderma gangrenosum (PG) is a sterile neutrophilic dermatosis manifesting as painful inflammatory plaques and ulcers, frequently associated with inflammatory bowel disease, rheumatoid arthritis, myelodysplastic syndrome, and acute myeloid leukemia.1 We present a case of a young woman with a novel mutation in NFkB1 who experienced common variable ...
Ian D. Odell   +8 more
openaire   +3 more sources

Herbal combination from Moringa oleifera Lam. and Curcuma longa L. as SARS-CoV-2 antiviral via dual inhibitor pathway: A viroinformatics approach. [PDF]

open access: yesJournal of Pharmacy & Pharmacognosy Research, 2022
Context: The COVID-19 outbreak is caused by the transmission and infection of SARS-CoV-2 at the end of 2019. It has led many countries to implement lockdown policies to prevent the viral spreading.
Viol Dhea Kharisma   +10 more
doaj  

Case Report: A child with NFKB1 haploinsufficiency explaining the linkage between immunodeficiency and short stature

open access: yesFrontiers in Immunology, 2023
We report the case of a patient with common variable immunodeficiency (CVID) presenting with short stature and treated with recombinant human growth hormone (rhGH).
S. Ricci   +19 more
doaj   +1 more source

Nfkb1 is a haploinsufficient DNA damage-specific tumor suppressor [PDF]

open access: yesOncogene, 2014
NF-κB proteins play a central and subunit-specific role in the response to DNA damage. Previous work identified p50/NF-κB1 as being necessary for cytotoxicity in response to DNA alkylation damage. Given the importance of damage-induced cell death for the maintenance of genomic stability, we examined whether Nfkb1 acts as a tumor suppressor in the ...
Adam M. Schmitt   +13 more
openaire   +3 more sources

Circ-NFKB1 sponges miR-203a-5p to regulate ERBB4 expression and promotes IL-1β induced chondrocytes apoptosis

open access: yesJournal of Orthopaedic Surgery and Research, 2023
Background Osteoarthritis (OA) is a chronic disease of the bones and joints that commonly affects middle-aged and elderly individuals, characterized by the degeneration of articular cartilage and inflammation of the joints. The molecular mechanisms of OA
Zhao Wang   +4 more
doaj   +1 more source

Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population [PDF]

open access: yes, 2020
Objectives: The cause of Meniere's disease (MD) is unclear but likely involves genetic and environmental factors. The aim of this study was to investigate the genetic basis underlying MD by screening putative candidate genes for MD.
Arweiler-Harbeck   +81 more
core   +1 more source

Association of NFKB1 gene rs28362491 mutation with the occurrence of major adverse cardiovascular events

open access: yesBMC Cardiovascular Disorders, 2022
Background Several studies have reported that NFKB1 gene rs28362491 polymorphism was associated with susceptibility to coronary heart disease in populations of different genetic backgrounds.
Jun-Yi Luo   +6 more
doaj   +1 more source

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