Tingting Gao

ORCID: 0000-0003-1112-0860
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About
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Research Areas
  • Retinal Diseases and Treatments
  • Ocular Diseases and Behçet’s Syndrome
  • Retinal Development and Disorders
  • Immune Cell Function and Interaction
  • DNA Repair Mechanisms
  • Nuclear Structure and Function
  • Glaucoma and retinal disorders
  • Renal and related cancers
  • Retinal and Optic Conditions
  • Otitis Media and Relapsing Polychondritis
  • Biosensors and Analytical Detection
  • Diabetes and associated disorders
  • Connexins and lens biology
  • Retinal Imaging and Analysis
  • Natural Language Processing Techniques
  • T-cell and B-cell Immunology
  • Systemic Lupus Erythematosus Research
  • Advanced biosensing and bioanalysis techniques
  • Quantum Dots Synthesis And Properties

Peking University
2018-2023

Capital Medical University
2023

Peking University Third Hospital
2020-2023

Nanjing Medical University
2023

Peking University People's Hospital
2018-2020

Nanjing University
2015

Wuhan University
2011

Zhongnan Hospital of Wuhan University
2011

In the present paper, we report that CdSe quantum dots (QDs) can act as coreactant of Ru(bpy)3(2+) electrogenerated chemiluminescence (ECL) in neutral condition. Strong anodic ECL signal was observed at ~1.10 V QDs modified glassy carbon electrode (CdSe/GCE), which might be mainly attributed to apparent electrocatalytic effect on oxidation Ru(bpy)3(2+). intercalated into loop hairpin DNA through electrostatic interaction fabricate a probe. When probe bound GCE, intense obtained. The more...

10.1038/srep15392 article EN cc-by Scientific Reports 2015-10-16

Several variants of CTLA-4 have been reported to be associated with susceptibility systemic lupus erythematosus (SLE); however, findings inconsistent across different populations. Using a case‐control study design, we investigated the role polymorphism at positions −1661 and −1722 on SLE in our Chinese population central China′s Hubei province. Samples were collected from 148 patients 170 healthy controls. Polymerase chain reaction restriction fragments length (PCR‐RFLP) was used analyze...

10.1155/2011/167395 article EN cc-by BioMed Research International 2011-01-01

Mutations in the gene BEST1 usually cause bestrophinopathies, such as rare progressive diseases Best vitelliform macular dystrophy (BVMD) and autosomal recessive bestrophinopathy (ARB). This study aimed to investigate clinical characteristics of patients with BVMD or ARB carrying mutations. A total 12 probands including 9 a diagnosis 3 were recruited for genetics analysis. All underwent detailed ophthalmic examination. coding exons screened by PCR-based DNA sequencing. Programs PolyPhen-2,...

10.1155/2018/4582816 article EN cc-by BioMed Research International 2018-10-18

To explore the clinical characteristics of Posner-Schlossman syndrome (PSS) patients in China, especially risk factors associated with dynamic changes corneal endothelial cell (CEC) density and retinal nerve fiber layer (RNFL) thickness during course disease.In this retrospective cohort study, consequently suffering from PSS were recruited. Patients data including gender, age onset, frequency attack, disease duration. We performed detailed ophthalmology examinations intraocular pressure...

10.1155/2023/4110344 article EN cc-by BioMed Research International 2023-01-01

Mathematical reasoning presents a significant challenge to the cognitive capabilities of LLMs. Various methods have been proposed enhance mathematical ability However, few recognize value state transition for LLM reasoning. In this work, we define problem-solving as process transiting from an initial unsolved final resolved state, and propose Kwai-STaR framework, which transforms LLMs into State-Transition Reasoners improve their intuitive capabilities. Our approach comprises three main...

10.48550/arxiv.2411.04799 preprint EN arXiv (Cornell University) 2024-11-07

Abstract Background: To analyze the association between central serous chorioretinopathy (CSCR) and single-nucleotide polymorphisms in complement factor H (CFH) gene patients of Chinese descent. Methods: 437 CSCR 510 controls were enrolled from Department Ophthalmology, People's Hospital Peking University. We genotyped each patient for six polymorphism (SNP) markers CFH (rs800292, rs1061170, rs3753396, rs2284664, rs1329428, rs1065489), assessed SNP's associations with CSCR. also performed a...

10.21203/rs.2.11402/v1 preprint EN cc-by Research Square (Research Square) 2019-07-15
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