Jinglei Zheng

22 Zhongguancun South Avenue
Haidian, 100081, China

Last Updated: 09/26/2026

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Found 10 publications

PARK7/HSPB1-Mediated Neuroprotective Effects of SHED in an In vitro Parkinson's Disease Model.

PARK7/HSPB1-Mediated Neuroprotective Effects of SHED in an In vitro Parkinson's Disease Model.

Journal: Neurochemical research

Published: June 15, 2026

KDF1 promotes ameloblast differentiation by inhibiting the IKK/IκB/NF-κB axis.

KDF1 promotes ameloblast differentiation by inhibiting the IKK/IκB/NF-κB axis.

Journal: Journal of cellular physiology

Published: March 28, 2024

BMPR2 Variants Underlie Nonsyndromic Oligodontia.

BMPR2 Variants Underlie Nonsyndromic Oligodontia.

Journal: International journal of molecular sciences

Published: November 02, 2022

Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern.

Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern.

Journal: Diagnostics (Basel, Switzerland)

Published: September 05, 2022

KDF1 Novel Variant Causes Unique Dental and Oral Epithelial Defects.

KDF1 Novel Variant Causes Unique Dental and Oral Epithelial Defects.

Journal: International journal of molecular sciences

Published: August 22, 2022

Four Novel PAX9 Variants and the PAX9-Related Non-Syndromic Tooth Agenesis Patterns.

Four Novel PAX9 Variants and the PAX9-Related Non-Syndromic Tooth Agenesis Patterns.

Journal: International journal of molecular sciences

Published: July 07, 2022

Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome.

Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome.

Journal: Archives of oral biology

Published: March 08, 2022

Novel MSX1 variants identified in families with nonsyndromic oligodontia.

Novel MSX1 variants identified in families with nonsyndromic oligodontia.

Journal: International journal of oral science

Published: May 27, 2020

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.

Journal: Human mutation

Published: May 13, 2020

Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders.

Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders.

Journal: Molecular genetics & genomic medicine

Published: January 14, 2019

Showing 1-10 of 10

Last Updated: 09/26/2026