A5101712953- MicroRNA in disease regulation
- Circular RNAs in diseases
- Birth, Development, and Health
- Liver Disease Diagnosis and Treatment
- Hormonal Regulation and Hypertension
- Peptidase Inhibition and Analysis
- Adipokines, Inflammation, and Metabolic Diseases
- Cardiovascular Disease and Adiposity
- Epilepsy research and treatment
- Prenatal Screening and Diagnostics
- Gestational Diabetes Research and Management
- Assisted Reproductive Technology and Twin Pregnancy
- Blood Pressure and Hypertension Studies
- Genetics and Neurodevelopmental Disorders
- Attention Deficit Hyperactivity Disorder
- Digital Transformation in Industry
- Extracellular vesicles in disease
- Gout, Hyperuricemia, Uric Acid
- Ginseng Biological Effects and Applications
- EEG and Brain-Computer Interfaces
- Electrochemical sensors and biosensors
- Translation Studies and Practices
- Autoimmune Neurological Disorders and Treatments
- Preterm Birth and Chorioamnionitis
- Traumatic Brain Injury and Neurovascular Disturbances
Sichuan University
2011-2024
Hubei University of Technology
2024
West China Second University Hospital of Sichuan University
2011-2024
Chengdu Medical College
2020-2022
First People’s Hospital of Jingmen
2022
Chongqing Medical University
2010-2021
The Affiliated Yongchuan Hospital of Chongqing Medical University
2015-2021
Chengdu University
2020
Nanfang Hospital
2016
Chongqing Public Health Medical Center
2011
Previous studies found elevated serum uric acid (SUA) was associated with the development or progression of non-alcoholic fatty liver disease (NAFLD) in general population; this study we aim to investigate association SUA and severity NAFLD based on grade ultrasonography non-obese subjects.Data were obtained from subjects via routine physical examinations Public Health Center our hospital between 2011 2014. The data included completed anthropometry blood biochemical indicators results...
Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) infection has many neurological manifestations, and its effects on the nervous system are increasingly recognized. There been no systematic analysis of electroencephalography (EEG) characteristics in children exhibiting symptoms Coronavirus disease 2019 (COVID-19). The primary aim this study was to describe EEG caused by COVID-19 who were showing assess relationship between COVID-19-related changes clinical...
The transforming growth factor β1 (TGF-β1)/SMAD family member 3 (SMAD3) pathway, and hypoxia-inducible 1α (HIF-1α) are two key players in various types of malignancies including breast cancer. TGF-β1/SMAD3 pathway can interact with HIF-1α some diseases; however, their interaction cancer is still unknown. Therefore, our study aimed to investigate the interactions between cancer.Expression serum patients healthy controls was detected by quantitative reverse transcription polymerase chain...
Background While both renin-dependent and renin-independent aldosterone secretion contribute to aldosteronism, their relative associations with cardiovascular disease (CVD) risk has not been investigated. Methods Results A total of 2909 participants from the FOS (Framingham Offspring Study) baseline, serum concentration, plasma renin concentration who attended sixth examination cycle were followed up until 2014 free CVD included. We further recruited 2612 hypertensive CONPASS (Chongqing...
Abstract Deficiency of adenosine deaminase 2 (DADA2) is a monogenic disease caused by biallelic mutations in (ADA2). The varying phenotypes the often lead to delayed diagnosis or misdiagnosis. We report an 11‐year‐old boy with DADA2 and provide preliminary analysis genotype–phenotype correlation. age onset was 8 years old. successively involved brainstem, muscles, joints, cerebrum. After three relapse–remission episodes over 3 years, patient finally diagnosed whole‐exome sequencing. Compound...
To explore the potential of using artificial intelligence (AI)-based eye tracking technology on a tablet for screening Attention-deficit/hyperactivity disorder (ADHD) symptoms in children.We recruited 112 children diagnosed with ADHD (ADHD group; mean age: 9.40 ± 1.70 years old) and 325 typically developing (TD 9.45 1.59 old). We designed data-driven end-to-end convolutional neural network appearance-based model to predict gaze permit eye-tracking under low resolution sampling rates. The...
Previous studies found famine exposure was associated with a higher risk of metabolic syndrome (MetS). In the study, we investigated relationship between Chinese and nonalcoholic fatty liver disease (NAFLD) in adult women. Data were obtained from subjects via routine physical examinations Public Health Center our hospital 2011 2014. Women categorized into following three groups: control, pre-natally exposed, postnatally exposed. Hepatic steatosis diagnosed according to guidelines established...
Chymotrypsin is one of the most extensively known proteases participating in pathogenesis various diseases, which can be used drug discovery and clinical diagnosis.
and C3435T) were assayed by PCR-RFLP.There significant differences in the distributions of 3435TT [P = 0.001; odds ratio 2.47; 95% confidence interval (CI) 1.44-4.27]and 3435CT < 0.28; 95%CI 0.15-0.54]genotypes between infantile spasm cases controls.No observed allelic haplotypic frequencies ABCB1 polymorphisms two groups.This study demonstrated that variations C3435T gene play an important role pathogenesis spasms Han Chinese population; is associated with increased risk having this...
More and more studies are investigating the influence of expression MicroRNA-21 (miRNA-21) on prognosis clinical significance in patients with lung cancer, but results contradictory uncertain. A meta-analysis was conducted controversial data to accurately assess issue.A detailed search relevant research Wanfang, Chinese Biomedical Literature Database, National Knowledge Infrastructure (CNKI), Chongqing VIP Science Technology Periodical PubMed, Embase, Web other databases. Two reviewers...
The opposition and unity of sound, meaning, form constitute the three elements language, that is, each language symbol contains aspects: form. Due to arbitrariness certain contradiction caused by &quot;less fewer forms, more meaning&quot;, relationship between these in system is not one-to-one, leading phenomenon polysemy homonym languages. Ambiguity a common linguistic exists both ancient modern languages, locally across It special structure meaning. Linguists believe ambiguity...
Microcephaly is a common nervous system malformation in pediatric outpatients, especially children with mental retardation. Till now, only few domestic researches reported about microcephaly. This paper reviews the abroad clinical, cellular and molecular biology diagnosis of microcephaly, order to provide references for clinical diagnosis, treatment further researches. Key words: Microcephaly; Diagnosis; Genetics; Child