Jin-wei He

600 Yishan Road
Shanghai, 200233, China

Last Updated: 09/26/2026

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Found 48 publications

Steroids Therapy in Patients With Severe COVID-19: Association With Decreasing of Pneumonia Fibrotic Tissue Volume.

Steroids Therapy in Patients With Severe COVID-19: Association With Decreasing of Pneumonia Fibrotic Tissue Volume.

Journal: Frontiers in medicine

Published: April 01, 2022

Genetic Polymorphisms of Nuclear Factor-κB Family Affect the Bone Mineral Density Response to Zoledronic Acid Therapy in Postmenopausal Chinese Women.

Genetic Polymorphisms of Nuclear Factor-κB Family Affect the Bone Mineral Density Response to Zoledronic Acid Therapy in Postmenopausal Chinese Women.

Journal: Genes

Published: February 27, 2022

Serum Periostin Level and Genetic Polymorphisms Are Associated with Vertebral Fracture in Chinese Postmenopausal Women.

Serum Periostin Level and Genetic Polymorphisms Are Associated with Vertebral Fracture in Chinese Postmenopausal Women.

Journal: Genes

Published: January 17, 2022

Usage of compromised lung volume in monitoring steroid therapy on severe COVID-19.

Usage of compromised lung volume in monitoring steroid therapy on severe COVID-19.

Journal: Respiratory research

Published: August 12, 2021

LGR4 Gene Polymorphisms Are Associated With Bone and Obesity Phenotypes in Chinese Female Nuclear Families.

LGR4 Gene Polymorphisms Are Associated With Bone and Obesity Phenotypes in Chinese Female Nuclear Families.

Journal: Frontiers in endocrinology

Published: January 25, 2021

Association between LGR4 polymorphisms and peak bone mineral density and body composition.

Association between LGR4 polymorphisms and peak bone mineral density and body composition.

Journal: Journal of bone and mineral metabolism

Published: September 07, 2019

Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese women.

Genetic variants in the PLS3 gene are associated with osteoporotic fractures in postmenopausal Chinese women.

Journal: Acta pharmacologica Sinica

Published: September 14, 2018

Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas.

Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas.

Journal: Endocrinology

Published: March 08, 2018

Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families.

Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families.

Journal: Acta pharmacologica Sinica

Published: January 19, 2017

Associations of Serum Osteocalcin and Polymorphisms of the Osteocalcin Gene with Bone Mineral Density in Postmenopausal and Elderly Chinese Women.

Associations of Serum Osteocalcin and Polymorphisms of the Osteocalcin Gene with Bone Mineral Density in Postmenopausal and Elderly Chinese Women.

Journal: Journal of nutrigenetics and nutrigenomics

Published: March 23, 2016

Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families.

Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families.

Journal: Journal of bone and mineral metabolism

Published: January 27, 2016

Osteomalacia induced by long-term low-dose adefovir dipivoxil: Clinical characteristics and genetic predictors.

Osteomalacia induced by long-term low-dose adefovir dipivoxil: Clinical characteristics and genetic predictors.

Journal: Bone

Published: January 24, 2016

Showing 1-12 of 48

Last Updated: 09/26/2026