Lv2
120 积分 2022-12-13 加入
Enhanced Chemiluminescence under the Nanoconfinement of CovalentOrganic Frameworks and Its Application in Sensitive Detection of Cancer Biomarkers
7个月前
已完结
Triple quenching effect of nanozyme catalyzed precipitation combined with enzyme-free amplification for photoelectrochemical biosensing of circulating tumor DNA
7个月前
已完结
A smartphone-enabled colorimetric tumor-derived exosomes sensing based on multi-enzyme catalysis and dual-recognition triggered CRISPR/Cas12a trans-cleavage
7个月前
已完结
Synergistic self-calibration strategy based on nano-cornucopia MOFs for accurate HER-2 detection in precision breast cancer diagnosis
7个月前
已完结
Triple quenching effect of nanozyme catalyzed precipitation combined with enzyme-free amplification for photoelectrochemical biosensing of circulating tumor DNA
8个月前
已完结
Dual Photoluminescence Emission Carbon Dots for Ratiometric Fluorescent GSH Sensing and Cancer Cell Recognition
8个月前
已完结
Recent Applications of Carbon Nanomaterials for microRNA Electrochemical Sensing
8个月前
已完结
Imaging Cellular Aerobic Glycolysis using Carbon Dots for Early Warning of Tumorigenesis
8个月前
已完结
Early Diagnosis of Triple-Negative Breast Cancer Based on Dual microRNA Detection Using a Well-Defined DNA Crown-Carbon Dots Structure as an Electrochemiluminescence Sensing Platform
8个月前
已完结
Tremella-derived carbon dots-based UV–vis/fluorescent dual-output sensing platform for multiplex miRNA detection
8个月前
已完结
Human-Induced Vibration Control with TMDs for Guangzhou Asian Games Comprehensive Museum
10个月前
已采纳
Estudo sobre a integridade superficial do aço ABNT 4140 após a operação de torneamento
10个月前
已采纳
Genomic analyses of germline and somatic variation in high-grade serous ovarian cancer
11个月前
已采纳
Compound genetic etiology in a patient with a syndrome including diabetes, intellectual deficiency and distichiasis
11个月前
已采纳
Clinical and genetic characterization of a cohort of 97 CLN6 patients tested at a single center
11个月前
已采纳
Revisiting the morbid genome of Mendelian disorders
11个月前
已采纳
Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease
11个月前
已采纳
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