Results 31 to 40 of about 20,611 (234)
Autoinflammatory disease with focus on NOD2-associated disease in the era of genomic medicine
Systemic autoinflammatory diseases (SAIDs) represent a spectrum of genetically heterogeneous inflammatory disorders. Some SAID-associated genes are located in chromosome 16, including familial Mediterranean fever gene (MEFV) and nucleotide-binding ...
Qingping Yao, Ellen Li, Bo Shen
doaj +1 more source
NOD2 polymorphisms may affect sensing of the bacterial muramyl dipeptide (MDP) and trigger perturbed inflammatory responses. Genetic screening of a patient with immunodeficiency and enteropathy revealed a rare homozygous missense mutation in the first ...
Maryam Ghalandary +16 more
doaj +1 more source
Yao syndrome (YAOS) is a systemic autoinflammatory disease (SAID), formerly termed nucleotide-binding oligomerization domain-2 (NOD2)-associated autoinflammatory disease.
Christine McDonald +4 more
doaj +1 more source
NOD2 attenuates osteoarthritis via reprogramming the activation of synovial macrophages
Objective Synovial inflammation, which precedes other pathological changes in osteoarthritis (OA), is primarily initiated by activation and M1 polarization of macrophages.
Changchuan Li +11 more
doaj +1 more source
Regulating the stabilities of NOD1 and NOD2, two innate immune receptors, with sugars and chaperones
Grimes, Catherine LeimkuhlerBahnson, Brian J.A healthy human body contains as many bacterial cells as it does human cells, and while some of these bacteria are known to cause diseases, many are beneficial and vital for our well-being, comprising the ...
Drake, Walter R., III
core +1 more source
We provide evidence here from loss-of-function studies in mice and gain-of-function studies in human cells (1, 2) which demonstrate control of UBE2Q2 by the NLR (nucleotide-binding oligomerization domain-like receptor) family protein NOD2.
openaire +1 more source
DataSheet_1_Blau syndrome NOD2 mutations result in loss of NOD2 cross-regulatory function.docx
The studies described here provide an analysis of the pathogenesis of Blau syndrome and thereby the function of NOD2 as seen through the lens of its dysfunction resulting from Blau-associated NOD2 mutations in its nucleotide-binding domain (NBD). As such,
Kim Montgomery-Recht (13798072) +8 more
core +1 more source
Identification of benzimidazole diamides as selective inhibitors of the nucleotide-binding oligomerization domain 2 (NOD2) signaling pathway. [PDF]
NOD2 is an intracellular pattern recognition receptor that assembles with receptor-interacting protein (RIP)-2 kinase in response to the presence of bacterial muramyl dipeptide (MDP) in the host cell cytoplasm, thereby inducing signals leading to the ...
David J Rickard +16 more
doaj +1 more source
NOD2 signalling in Crohn's disease [PDF]
Introduction NOD2 is an intracellular pattern recognition receptor that induces autophagy in human dendritic cells (DCs) in a manner important for bacterial handling and antigen presentation. Variants of NOD2 associated with terminal ileal Crohn's disease (CD) fail to induce autophagy normally on Nod2 stimulation ...
Allan, P +9 more
openaire +1 more source
Human NOD2 Recognizes Structurally Unique Muramyl Dipeptides from Mycobacterium leprae. [PDF]
The innate immune system recognizes microbial pathogens via pattern recognition receptors. One such receptor, NOD2, via recognition of muramyl dipeptide (MDP), triggers a distinct network of innate immune responses, including the production of ...
Schenk, Mirjam +15 more
core +1 more source

