Dongye He

89 Guhuai Road
Jining, 272029, China

Last Updated: 09/26/2026

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Found 17 publications

A novel splice-altering frameshift variant in the COL1A1 gene underlies osteogenesis imperfecta type I: molecular characterization of a four-generation Chinese pedigree and literature review.

A novel splice-altering frameshift variant in the COL1A1 gene underlies osteogenesis imperfecta type I: molecular characterization of a four-generation Chinese pedigree and literature review.

Journal: Human genomics

Published: May 14, 2025

Identification and functional analysis of NPR2 truncating mutations in two Chinese families with short stature.

Identification and functional analysis of NPR2 truncating mutations in two Chinese families with short stature.

Journal: BMC pediatrics

Published: October 15, 2024

Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndrome.

Functional investigation of a novel ANKRD11 frameshift variant identified in a Chinese family with KBG syndrome.

Journal: Heliyon

Published: October 30, 2023

Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency.

Identification and functional analysis of first heterozygous frameshift mutation in the GHRH gene in a Chinese boy with isolated growth hormone deficiency.

Journal: Gene

Published: October 24, 2023

Letrozole combined with rhGH treatment increases the adult height of short pubertal boys.

Letrozole combined with rhGH treatment increases the adult height of short pubertal boys.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: October 14, 2023

Clinical Manifestations, Genetic Variants and Therapeutic Evaluation in Sporadic Chinese Patients with Idiopathic Hypogonadotropic Hypogonadism.

Clinical Manifestations, Genetic Variants and Therapeutic Evaluation in Sporadic Chinese Patients with Idiopathic Hypogonadotropic Hypogonadism.

Journal: International journal of general medicine

Published: July 16, 2023

Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search.

Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search.

Journal: Orphanet journal of rare diseases

Published: April 03, 2023

Serum triglyceride glucose index is a valuable predictor for visceral obesity in patients with type 2 diabetes: a cross-sectional study.

Serum triglyceride glucose index is a valuable predictor for visceral obesity in patients with type 2 diabetes: a cross-sectional study.

Journal: Cardiovascular diabetology

Published: March 09, 2023

Association Between the Growth Hormone/Insulin-Like Growth Factor-1 Axis and Muscle Density in Children and Adolescents of Short Stature.

Association Between the Growth Hormone/Insulin-Like Growth Factor-1 Axis and Muscle Density in Children and Adolescents of Short Stature.

Journal: Frontiers in endocrinology

Published: April 14, 2022

Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone.

Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: October 28, 2021

Toxicological Evaluation of Camellia euphlebia Leaves Aqueous Extract Using Acute and Subacute Toxicity Studies in Mice and Genotoxicity Studies.

Toxicological Evaluation of Camellia euphlebia Leaves Aqueous Extract Using Acute and Subacute Toxicity Studies in Mice and Genotoxicity Studies.

Journal: Evidence-based complementary and alternative medicine : eCAM

Published: August 10, 2021

Corilagin induces apoptosis and inhibits autophagy of HL‑60 cells by regulating miR‑451/HMGB1 axis.

Corilagin induces apoptosis and inhibits autophagy of HL‑60 cells by regulating miR‑451/HMGB1 axis.

Journal: Molecular medicine reports

Published: December 31, 2020

Showing 1-12 of 17

Last Updated: 09/26/2026