Xinjie Zhang

Tianjin, 300387, China

Last Updated: 09/26/2026

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Found 12 publications

Low hysteresis and high sensitivity TPU/carbonized wood cellulose sponge sensors for monitoring dynamic pulses.

Low hysteresis and high sensitivity TPU/carbonized wood cellulose sponge sensors for monitoring dynamic pulses.

Journal: International journal of biological macromolecules
Published: October 24, 2024

Serum vitamin D3 deficiency can affect the efficacy of sublingual immunotherapy in children with allergic rhinitis: a retrospective cohort study.

Serum vitamin D3 deficiency can affect the efficacy of sublingual immunotherapy in children with allergic rhinitis: a retrospective cohort study.

Journal: Journal of thoracic disease
Published: December 02, 2022

Identification of a Splicing Variant c.3813-3A>G in NPHP3 by Reanalysis of Whole Exome Sequencing in a Chinese Boy with Nephronophthisis.

Identification of a Splicing Variant c.3813-3A>G in NPHP3 by Reanalysis of Whole Exome Sequencing in a Chinese Boy with Nephronophthisis.

Journal: Nephron
Published: July 31, 2022

Analysis of gene variant in an infant with succinic semialdehyde dehydrogenase deficiency

Analysis of gene variant in an infant with succinic semialdehyde dehydrogenase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 25, 2022

Phenotypic and genotypic analysis of children with methylmalonic academia: A single-center study in China and a recent literature review.

Phenotypic and genotypic analysis of children with methylmalonic academia: A single-center study in China and a recent literature review.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: May 28, 2021

Genetic analysis of a child with very long chain acyl-CoA dehydrogenase deficiency

Genetic analysis of a child with very long chain acyl-CoA dehydrogenase deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 21, 2020

Rapid screening of a hotspot variant c.609G>A in MMACHC gene by using PCR-high-resolution melting curve analysis

Rapid screening of a hotspot variant c.609G>A in MMACHC gene by using PCR-high-resolution melting curve analysis

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 04, 2020

The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l-hydroxylase deficiency in a Chinese cohort.

The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l-hydroxylase deficiency in a Chinese cohort.

Journal: Molecular genetics & genomic medicine
Published: May 18, 2020

Variants of CAPN3 cause limb-girdle muscular dystrophy type 2A in two Chinese families.

Variants of CAPN3 cause limb-girdle muscular dystrophy type 2A in two Chinese families.

Journal: Experimental and therapeutic medicine
Published: February 17, 2020

Rapid screening of UPB1 gene variations by high resolution melting curve analysis.

Rapid screening of UPB1 gene variations by high resolution melting curve analysis.

Journal: Experimental and therapeutic medicine
Published: February 12, 2020

Rapid screening of MMACHC gene mutations by high-resolution melting curve analysis.

Rapid screening of MMACHC gene mutations by high-resolution melting curve analysis.

Journal: Molecular genetics & genomic medicine
Published: August 04, 2019

Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature review.

Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature review.

Journal: European journal of medical genetics
Published: December 23, 2018
Showing 1-12 of 12

Last Updated: 09/26/2026