Results 191 to 200 of about 23,374 (217)

Circulating endotoxin is correlated with fatty acid binding protein 2 and leukocyte nuclear factor-κB activation in menopausal women. [PDF]

Sci Rep
Chen TY, Huang WY, Liu KH, Lin S, Wu HM.
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Integrative Discovery Through Network Pharmacology and Molecular Docking Approaches of Phenolic Compounds Isolated from <i>Torreya nucifera</i> to Treat Rheumatoid Arthritis. [PDF]

Int J Mol Sci
Le DD, Dang T, Truong V, Yu S, Yang SH, Choi MH, Lee M.   +6 more
europepmc   +1 more source

Integration of urine retinol-binding protein and genetic markers for early prediction of tacrolimus nephrotoxicity using machine learning. [PDF]

Transl Pediatr
Miao Y, Chen X, Xie P, Liang Y, Wei Y, Deng H, Huang Q, Qiu H, Li H, Zhou S, Liang H, Huang M, Li J, Gao X, Mo X.   +14 more
europepmc   +1 more source

Reconstruction and analysis of the gene network regulating apoptosis in hepatocellular carcinoma based on scRNA-seq data and the ANDSystem knowledge base. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Adamovskaya AV, Yatsyk IV, Kleshchev MA, Demenkov PS, Ivanisenko TV, Ivanisenko VA.   +5 more
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Role of the Inflammasome Pathway According to the Expression of Proteins and Genetic Polymorphisms in COVID-19 Patients. [PDF]

Int J Mol Sci
Dos Santos TR, Carstens LB, Barbosa LV, Collete M, de Araujo N, de Paula CBV, Azevedo MLV, de Almeida AC, Nagashima S, de Noronha L, Machado-Souza C.   +10 more
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The Influence of Reactive Oxygen Species in the Development of Contrast-Induced Nephropathy After Coronary Angiography. [PDF]

J Clin Med
Dheir H, Guney Eskiler G, Tocoğlu A, Kurt R, Gonullu E, Nalbant A, Gunduz H, Tamer A.   +7 more
europepmc   +1 more source

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Combined immunodeficiency caused by a novel homozygous NFKB1 mutation

Journal of Allergy and Clinical Immunology, 2021
Genetic faults in several components of the nuclear factor-κB pathway cause immunodeficiency. Most defects lead to combined immunodeficiency with a range of severity. Heterozygous mutations in NFKB1 were associated with common variable immunodeficiency, however, homozygous mutations have not been described.We studied the molecular basis of combined ...
Amarilla B, Mandola, Nigel, Sharfe, Zahra, Nagdi, Harjit, Dadi, Linda, Vong, Daniele, Merico, Bo, Ngan, Brenda, Reid, Chaim M, Roifman   +8 more
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Convergent lines of evidence supporting involvement of NFKB1 in schizophrenia

Psychiatry Research, 2022
NFKB1 was associated with treatment-refractory schizophrenia (SZ) and response to antipsychotics; however, the underlying mechanisms through which NFKB1 confers its risk for SZ are largely unknown. We aimed to investigate the potential role of NFKB1 in SZ.In the present study, we investigated the association of the risk SNP rs230529 of NFKB1 with gray ...
Jing Long, Lin Tian, Ancha Baranova, Hongbao Cao, Yao Yao, Shuquan Rao, Fuquan Zhang   +6 more
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Identification of novel NFKB1 and ICOS frameshift variants in patients with CVID

Clinical and Experimental Immunology, 2022
AbstractCommon variable immunodeficiency (CVID) is a ‘late-onset’ primary immunodeficiency characterized by variable manifestations and genetic heterogeneity. A monogenic cause of CVID has been reported in 10% of patients. In this study, we identified two novel pathogenic variants implicated in monogenic CVID by whole exome sequencing (WES) analysis: a
Anli Liu, Qiang Liu, Shaoqiu Leng, Xiaoyu Zhang, Qi Feng, Jun Peng, Gege Feng   +6 more
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