Qi Zhou

Luzhou, 646000, China

Last Updated: 09/26/2026

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Found 13 publications

Novel compound heterozygous missense variants (c.G955A and c.A1822C) of CACNA2D4 likely causing autosomal recessive retinitis pigmentosa in a Chinese patient.

Novel compound heterozygous missense variants (c.G955A and c.A1822C) of CACNA2D4 likely causing autosomal recessive retinitis pigmentosa in a Chinese patient.

Journal: 3 Biotech

Published: December 23, 2020

Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA.

Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA.

Journal: Molecular medicine reports

Published: January 08, 2020

Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient.

Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient.

Journal: Frontiers in genetics

Published: October 19, 2019

Novel compound heterozygous EYS variants may be associated with arRP in a large Chinese pedigree.

Novel compound heterozygous EYS variants may be associated with arRP in a large Chinese pedigree.

Journal: Bioscience reports

Published: October 02, 2019

A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa.

A novel missense variant c.G644A (p.G215E) of the RPGR gene in a Chinese family causes X-linked retinitis pigmentosa.

Journal: Bioscience reports

Published: July 11, 2019

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.

A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.

Journal: Journal of cellular and molecular medicine

Published: December 20, 2018

A High-Accuracy AlGaN/GaN Reverse Blocking CRD (RB-CRD) with Hybrid Trench Cathode.

A High-Accuracy AlGaN/GaN Reverse Blocking CRD (RB-CRD) with Hybrid Trench Cathode.

Journal: Nanoscale research letters

Published: December 02, 2018

Testosterone-Dependent miR-26a-5p and let-7g-5p Act as Signaling Mediators to Regulate Sperm Apoptosis via Targeting PTEN and PMAIP1.

Testosterone-Dependent miR-26a-5p and let-7g-5p Act as Signaling Mediators to Regulate Sperm Apoptosis via Targeting PTEN and PMAIP1.

Journal: International journal of molecular sciences

Published: March 20, 2018

The Resistance-Amplitude-Frequency Effect of In-Liquid Quartz Crystal Microbalance.

The Resistance-Amplitude-Frequency Effect of In-Liquid Quartz Crystal Microbalance.

Journal: Sensors (Basel, Switzerland)

Published: May 10, 2017

Investigation of Bulk Traps by Conductance Method in the Deep Depletion Region of the Al2O3/GaN MOS Device.

Investigation of Bulk Traps by Conductance Method in the Deep Depletion Region of the Al2O3/GaN MOS Device.

Journal: Nanoscale research letters

Published: February 22, 2017

Establishment and rapid detection of a heterozygous missense mutation in the CACNA1F gene by ARMS technique with double-base mismatched primers.

Establishment and rapid detection of a heterozygous missense mutation in the CACNA1F gene by ARMS technique with double-base mismatched primers.

Journal: Genetics and molecular research : GMR

Published: October 06, 2015

Identification of a novel heterozygous missense mutation in the CACNA1F gene in a chinese family with retinitis pigmentosa by next generation sequencing.

Identification of a novel heterozygous missense mutation in the CACNA1F gene in a chinese family with retinitis pigmentosa by next generation sequencing.

Journal: BioMed research international

Published: August 03, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026