A5083831909- Immune Cell Function and Interaction
- Immune Response and Inflammation
- T-cell and B-cell Immunology
- Cancer-related molecular mechanisms research
- Glaucoma and retinal disorders
- IL-33, ST2, and ILC Pathways
- Cardiac electrophysiology and arrhythmias
- Ocular Surface and Contact Lens
- Retinal Diseases and Treatments
- Nitric Oxide and Endothelin Effects
- Hepatocellular Carcinoma Treatment and Prognosis
- Liver Disease Diagnosis and Treatment
- ECG Monitoring and Analysis
- Microscopic Colitis
- Advanced Measurement and Detection Methods
- RNA and protein synthesis mechanisms
- Thyroid Disorders and Treatments
- MRI in cancer diagnosis
- Obstructive Sleep Apnea Research
- Ophthalmology and Visual Impairment Studies
- Corneal surgery and disorders
- Advanced machining processes and optimization
- Viral Infections and Immunology Research
- Synthesis of β-Lactam Compounds
- Chemokine receptors and signaling
Qingdao University
2024
Affiliated Hospital of Qingdao University
2024
Capital Medical University
1995-2023
Beijing Shijitan Hospital
2022
University of Oxford
2004-2021
Science Oxford
2021
Beijing Ditan Hospital
2014-2019
Beijing Tongren Hospital
2007-2017
Beijing Anzhen Hospital
2014
The Ohio State University
2003
<h3>BACKGROUND AND PURPOSE:</h3> Currently, there is no effective treatment for pediatric patients with complete spinal cord injury. Motor imagery has been proposed as an alternative to physical training who are unable move voluntarily. Our aim was reveal the potential mechanism of motor in rehabilitation <h3>MATERIALS METHODS:</h3> Twenty-six injury and 26 age- sex-matched healthy children controls were recruited. All participants underwent task-related fMRI scans, additional execution...
We assessed the possible correlation between genetic polymorphisms in interleukin (IL)-1β, IL-8, and IL-10 risk of acute pancreatitis. Polymorphisms IL-1β+3954C/T (rs1143634), IL-1β-511C/T (rs16944), IL-8 -251T/A (rs4073), -1082A/G (rs1800896), -819C/T (rs1800871) were by polymerase chain reaction-restriction fragment length polymorphism. Patients with pancreatitis more likely to have a family history habit tobacco smoking alcohol drinking. Conditional logistic regression analyses showed...
<h3>Aim:</h3> To evaluate utility values among patients of primary angle closure/glaucoma (PAC/G) in a local hospital China, and the factors influencing quality their lives. <h3>Methods:</h3> A cross-sectional study. Utility were measured using time trade-off (TTO) standard gamble (gamble for blindness) methods. Standard face-to-face interviews conducted. Results ophthalmic examinations recorded. <h3>Results:</h3> One hundred six recruited, 16 (15.1%) male 90 (84.9%) female, mean age 63.21...
Objective: To explore the correlation between portal vein pressure gradient (PPG) and hepatic (HVPG) in patients with hypertension (PHT). Methods: 752 cases (PHT) who underwent transjugular intrahepatic portosystemic shunt (TIPS) met enrollment criteria January 2016 to December 2019 were analyzed for vein, inferior vena cava pressure. Paired t-test was used analysis. Pearson test estimate coefficient of determination. P<0.05 considered statistically significant. Results: Wedged (WHVP),...
Summary A minority of hand, foot and mouth disease (HFMD) caused by enterovirus A71 (EV-A71) results in severe neural complications. However, whether monocyte-mediated immunity is involved the progression HFMD remains unknown. One hundred twenty mild 103 patients were recruited enzyme-linked immunosorbent assay (ELISA), flow cytometry Transwell culture performed study. Peripheral monocyte counts lower both absolute frequencies cases compared to cases. After screening 10 monocyte-related...
KIR3DL1 *0150208 possesses five point mutations: 3037G >A, 4115A >G, 6053G >C, 8034A and 9446T >C compared to *0150201 .
Thyroid associated ophthalmopathy (TAO) is a common complication of Graves' disease (GD). The clinical manifestations are mainly swelling and retracted eyelid, protopsis limited eye movements, optic neuropathy can be seen in severe cases. mechanism TAO not yet clear. A large number studies have found that the disorders autoimmunity play an important role TAO, while genetic factors, oxidative stress, environmental factors such as smoking participate it. Therefore, we consult expound...
This study aimed to investigate the effect of laser peripheral iridotomy (LPI) on intraocular lens (IOL) power in patients with primary angle closure disease (PACD), and construct mathematical models assess changes IOL power.
KIR3DL1 *0150207 differs from *0150201 at five nucleotide positions in introns 2, 3, 4 and 5, respectively.
The new KIR3DL1 *0200101 differs from *01502 with 12 single nucleotide polymorphisms ( SNPs ) in two exons and seven introns.
KIR3DL1 *0150205 and *0150206 alleles have five six mutations, respectively, compared with *0150201 .
Abstract Funding Acknowledgements Type of funding sources: Foundation. Main source(s): Wellcome Trust Background Sudden cardiac death after a myocardial infarction (MI) was reported in both the acute stage and chronic with development heart failure (HF). Around 50% these deaths were due to ventricular tachyarrhythmia which is related temporal dispersion repolarisation caused by post-MI remodelling ionic currents. While variable extent current changes observed multiple animal species...
The novel KIR3DS1 *0130106 differs from *0130101 with a single point mutation at position 7211 (G>T).
KIR3DS1 *0130108 possesses three SNPs at: 12548C >G, 13804C >G and 13819G >A (introns 6 7, respectively) compared to *0130101 .
KIR3DS1 *0130105 allele differs from *0130101 with a single mutation at position 6739G >T of intron 5.
KIR3DS1 *0130111 differs from *0130101 with two previously undescribed single nucleotide polymorphisms.
KIR3DS1*0130110 differs from KIR3DS1*0130101 with two nucleotide substitutions at positions 7322 (G > T) and 12617 (C A), respectively.
Summary This novel KIR 3 DS 1 allele officially named as 1*0130107 was isolated from DNA samples A sia using high‐resolution sequenced‐based techniques. differs the first member of 1*013 subgroup ( 1*0130101 ) by a single mutation at position 8922A>G (intron 5), just nine nucleotides away start exon 6.