Results 101 to 110 of about 21,043 (239)
NFKB1 gene rs28362491 polymorphism is associated with the susceptibility of acute coronary syndrome [PDF]
Abstract The acute coronary syndrome (ACS) is a complex disease where genetic and environmental factors are involved. NF-κB, a central regulator of inflammation, is involved in various inflammatory diseases. The aim of the present study was to explore the association between NFKB1 gene rs28362491 (-94ATTGins/del) polymorphism and ACS.
Si-Yu Jin+6 more
openaire +3 more sources
Background Innate immune responses induced by in vitro stimulation of primary mammary epithelial cells (MEC) using Gram-negative lipopolysaccharide (LPS) and Gram-positive lipoteichoic acid (LTA) bacterial cell wall components are well- characterized in
Omar Bulgari+4 more
doaj +1 more source
Identification of Novel Type 2 Diabetes Candidate Genes Involved in the Crosstalk between the Mitochondrial and the Insulin Signaling Systems [PDF]
Type 2 Diabetes (T2D) is a highly prevalent chronic metabolic disease with strong co-morbidity with obesity and cardiovascular diseases. There is growing evidence supporting the notion that a crosstalk between mitochondria and the insulin signaling ...
+18 more
core +3 more sources
Metastasis in head and neck squamous cell carcinoma (HNSC) poses significant clinical challenges. This proof‐of‐concept study establishes patient‐derived orthotopic xenografts (PDOXs) as advanced models that closely replicate primary HNSC tumours, including local lymph node metastasis and the intricate cancer–stroma interaction.
Yuchen Bai+5 more
wiley +1 more source
Association of NFKB1 and NFKBIA gene polymorphisms with susceptibility of gastric cancer [PDF]
Xianyou county of Fujian province, located on the southeast coastal of China, has higher gastric cancer mortality. Chronic inflammation plays an important role in the occurrence of gastric cancer, in which the nuclear factor-κB signaling pathway of the inflammatory reaction begins and plays an important role in the amplification process.
Baoying Liu+3 more
openaire +3 more sources
Objective ― The aim of the study was to investigate the relationship of the alleles and genotypes of the immune response mediator genes polymorphic loci (rs1800629, rs909253, rs16944, rs6822844, rs2104286, rs1800795, rs1800872, rs3087243, rs755622 ...
Liliia Sh. Nazarova+4 more
doaj +1 more source
Genome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and function. [PDF]
Oculocutaneous syndromes are often due to mutations in single genes. In some cases, mouse models for these diseases exist in spontaneously occurring mutations, or in mice resulting from forward mutatagenesis screens.
Adissu, Hibret+15 more
core
ABSTRACT Background Artificial intelligence (AI) and various subunits of AI such as artificial neural networks (ANN), Convolutional neural networks (CNNs), machine learning (ML), deep learning (DL) and deep neural networks (DNN) are being tried to diagnose and plan treatment for periodontal diseases.
Rupanjan Roy+3 more
wiley +1 more source
Genome-wide association study of treatment refractory schizophrenia in Han Chinese. [PDF]
We report the first genome-wide association study of a joint analysis using 795 Han Chinese individuals with treatment-refractory schizophrenia (TRS) and 806 controls. Three loci showed suggestive significant association with TRS were identified.
Ying-Jay Liou+22 more
doaj +1 more source
Exome analysis of rare and common variants within the NOD signaling pathway [PDF]
Pediatric inflammatory bowel disease (pIBD) is a chronic heterogeneous disorder. This study looks at the burden of common and rare coding mutations within 41 genes comprising the NOD signaling pathway in pIBD patients.
Afzal, Nadeem A.+10 more
core +1 more source