Zhiqing Hu

110 Xiangya Road
Changsha, 410078, China

Last Updated: 09/26/2026

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Found 33 publications

Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder.

Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder.

Journal: Science advances

Published: June 17, 2026

FOCUS: A Dual-Mismatch crRNA Strategy Unlocks High-Fidelity One-Step SNV Detection with Cas12a.

FOCUS: A Dual-Mismatch crRNA Strategy Unlocks High-Fidelity One-Step SNV Detection with Cas12a.

Journal: ACS sensors

Published: April 21, 2026

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder.

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder.

Journal: Science bulletin

Published: December 19, 2025

CRISPR/Cas12a-Based Biosensing: Advances in Mechanisms and Applications for Nucleic Acid Detection.

CRISPR/Cas12a-Based Biosensing: Advances in Mechanisms and Applications for Nucleic Acid Detection.

Journal: Biosensors

Published: April 21, 2025

Overexpression of NKG2D and IL24 in NK Cell-Derived Exosomes for Cancer Therapy.

Overexpression of NKG2D and IL24 in NK Cell-Derived Exosomes for Cancer Therapy.

Journal: International journal of molecular sciences

Published: January 29, 2025

Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A.

Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A.

Journal: International journal of molecular sciences

Published: February 13, 2024

Rapid and sensitive Cas12a-based one-step nucleic acid detection with ssDNA-modified crRNA.

Rapid and sensitive Cas12a-based one-step nucleic acid detection with ssDNA-modified crRNA.

Journal: Analytica chimica acta

Published: May 04, 2023

CRISPR-Mediated In Situ Introduction or Integration of F9-Padua in Human iPSCs for Gene Therapy of Hemophilia B.

CRISPR-Mediated In Situ Introduction or Integration of F9-Padua in Human iPSCs for Gene Therapy of Hemophilia B.

Journal: International journal of molecular sciences

Published: April 08, 2023

A protospacer adjacent motif-free, multiplexed, and quantitative nucleic acid detection platform with barcode-based Cas12a activity.

A protospacer adjacent motif-free, multiplexed, and quantitative nucleic acid detection platform with barcode-based Cas12a activity.

Journal: MedComm

Published: January 10, 2023

Correction of F8 intron 1 inversion in hemophilia A patient-specific iPSCs by CRISPR/Cas9 mediated gene editing.

Correction of F8 intron 1 inversion in hemophilia A patient-specific iPSCs by CRISPR/Cas9 mediated gene editing.

Journal: Frontiers in genetics

Published: December 04, 2022

Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism.

Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism.

Journal: International journal of molecular sciences

Published: October 06, 2022

Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and Cardiomyocytes.

Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and Cardiomyocytes.

Journal: International journal of molecular sciences

Published: July 18, 2022

Showing 1-12 of 33

Last Updated: 09/26/2026