Zhangzhang Lan

1088 Xueyuan Rd
Shenzhen, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 19 publications

NID2 Affects Prognosis of Glioma via Activating the Akt Signaling Pathway.

NID2 Affects Prognosis of Glioma via Activating the Akt Signaling Pathway.

Journal: International journal of molecular sciences

Published: February 28, 2025

CPEB1 Controls NRF2 Proteostasis and Ferroptosis Susceptibility in Pancreatic Cancer.

CPEB1 Controls NRF2 Proteostasis and Ferroptosis Susceptibility in Pancreatic Cancer.

Journal: International journal of biological sciences

Published: March 05, 2024

Copy number variants landscape of multiple cancers and clinical applications based on NGS gene panel.

Copy number variants landscape of multiple cancers and clinical applications based on NGS gene panel.

Journal: Annals of medicine

Published: November 15, 2023

Comprehensive bioinformatics analysis of functional molecules in colorectal cancer.

Comprehensive bioinformatics analysis of functional molecules in colorectal cancer.

Journal: Journal of gastrointestinal oncology

Published: December 05, 2021

Serum metabolomic and lipidomic profiling identifies diagnostic biomarkers for seropositive and seronegative rheumatoid arthritis patients.

Serum metabolomic and lipidomic profiling identifies diagnostic biomarkers for seropositive and seronegative rheumatoid arthritis patients.

Journal: Journal of translational medicine

Published: August 15, 2021

A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review.

A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review.

Journal: BMC endocrine disorders

Published: June 25, 2020

Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing.

Analysis of a Chinese Pedigree With Familial Chylomicronemia Syndrome Reveals Two Novel LPL Mutations by Whole-Exome Sequencing.

Journal: Frontiers in genetics

Published: May 09, 2020

CPVA: a web-based metabolomic tool for chromatographic peak visualization and annotation.

CPVA: a web-based metabolomic tool for chromatographic peak visualization and annotation.

Journal: Bioinformatics (Oxford, England)

Published: November 29, 2019

Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing.

Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non-invasive prenatal testing.

Journal: Prenatal diagnosis

Published: July 18, 2017

Syntool: A Novel Region-Based Intolerance Score to Single Nucleotide Substitution for Synonymous Mutations Predictions Based on 123,136 Individuals.

Syntool: A Novel Region-Based Intolerance Score to Single Nucleotide Substitution for Synonymous Mutations Predictions Based on 123,136 Individuals.

Journal: BioMed research international

Published: May 02, 2017

Clinical, biochemical and molecular analysis of two infants with familial chylomicronemia syndrome.

Clinical, biochemical and molecular analysis of two infants with familial chylomicronemia syndrome.

Journal: Lipids in health and disease

Published: November 21, 2015

A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencing.

A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencing.

Journal: Neuromuscular disorders : NMD

Published: November 25, 2014

Showing 1-12 of 19

Last Updated: 09/26/2026