Yifang Huang

Key Laboratory Of Clinical Laboratory Medicine Of Guangxi Medical University
Nanning, 530021, China

Last Updated: 09/26/2026

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Found 12 publications

Ultrasensitive Single-Molecule Immunoassays Built on Digital Techniques for Low Amounts of Biomarker Detection.

Ultrasensitive Single-Molecule Immunoassays Built on Digital Techniques for Low Amounts of Biomarker Detection.

Journal: ACS sensors

Published: August 05, 2025

Assessment of hospital environmental and personal protective equipment contamination with influenza A and B viruses by ultrasensitive droplet digital PCR.

Assessment of hospital environmental and personal protective equipment contamination with influenza A and B viruses by ultrasensitive droplet digital PCR.

Journal: Diagnostic microbiology and infectious disease

Published: April 04, 2025

Case report: Novel multi-exon homozygous deletion of ZBTB24 causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2.

Case report: Novel multi-exon homozygous deletion of ZBTB24 causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2.

Journal: Frontiers in immunology

Published: October 26, 2024

Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762].

Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762].

Journal: Gene

Published: August 30, 2024

Detection of hemophilia A genetic variants using third-generation long-read sequencing.

Detection of hemophilia A genetic variants using third-generation long-read sequencing.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 19, 2024

A novel discriminant algorithm for differential diagnosis of mild to moderate thalassemia and iron deficiency anemia.

A novel discriminant algorithm for differential diagnosis of mild to moderate thalassemia and iron deficiency anemia.

Journal: Medicine

Published: May 17, 2024

A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome.

A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome.

Journal: Gene

Published: January 31, 2024

Third-generation sequencing for genetic disease.

Third-generation sequencing for genetic disease.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: August 07, 2023

Non-syndromic enlarged vestibular aqueduct caused by novel compound mutations of the SLC26A4 gene: a case report and literature review.

Non-syndromic enlarged vestibular aqueduct caused by novel compound mutations of the SLC26A4 gene: a case report and literature review.

Journal: Frontiers in genetics

Published: June 15, 2023

An enzyme-activatable dual-readout probe for sensitive β-galactosidase sensing and Escherichia coli analysis.

An enzyme-activatable dual-readout probe for sensitive β-galactosidase sensing and Escherichia coli analysis.

Journal: Frontiers in bioengineering and biotechnology

Published: September 24, 2022

A Blood-Responsive AIE Bioprobe for the Ultrasensitive Detection and Assessment of Subarachnoid Hemorrhage.

A Blood-Responsive AIE Bioprobe for the Ultrasensitive Detection and Assessment of Subarachnoid Hemorrhage.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: September 19, 2022

MiR-199a-3p/5p participated in TGF-β and EGF induced EMT by targeting DUSP5/MAP3K11 in pterygium.

MiR-199a-3p/5p participated in TGF-β and EGF induced EMT by targeting DUSP5/MAP3K11 in pterygium.

Journal: Journal of translational medicine

Published: April 25, 2020

Showing 1-12 of 12

Last Updated: 09/26/2026