J. Gu

发表

The A242T mutation in the low-density lipoprotein receptor-related protein 5 gene in one Chinese family with osteosclerosis.

Bao-Hong Zhang, Zhenlin Zhang, Jin-wei He, 2013, Internal medicine.

Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese women

Wei-wei Hu, Yujuan Liu, Zhenlin Zhang, 2012, Menopause.

No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women

Zhenlin Zhang, Jin-wei He, H. Yue, 2011, Acta Pharmacologica Sinica.

Prevalence of Vitamin D Inadequacy Among Chinese Postmenopausal Women: A Nationwide, Multicenter, Cross-Sectional Study

J. Chandler, W. Xia, Zhenlin Zhang, 2019, Front. Endocrinol..

Genetics Evaluation of Targeted Exome Sequencing in 223 Chinese Probands With Genetic Skeletal Dysplasias

Shan-shan Li, Wei-wei Hu, Zhenlin Zhang, 2021, Frontiers in Cell and Developmental Biology.

Lean mass predicts hip geometry and bone mineral density in chinese men and women and age comparisons of body composition.

Wei-wei Hu, Zhenlin Zhang, H. Yue, 2012, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.

Wei-wei Hu, Yujuan Liu, W. Xia, 2012, American journal of human genetics.

Hip axis length changes in 10,554 males and females and the association with femoral neck fracture.

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2008, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Genetic polymorphisms in the mevalonate pathway affect the therapeutic response to alendronate treatment in postmenopausal Chinese women with low bone mineral density

H. Zhang, Y.-J. Liu, H. Yue, 2014, The Pharmacogenomics Journal.

Thirteen Chinese patients with sporadic Paget’s disease of bone: clinical features, SQSTM1 mutation identification, and functional analysis

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of Bone and Mineral Metabolism.

Susceptibility genes for osteoporotic fracture in postmenopausal chinese women

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Comparison of the effects of cholecalciferol and calcitriol on calcium metabolism and bone turnover in Chinese postmenopausal women with vitamin D insufficiency

Zhenlin Zhang, Hao Zhang, Jie-mei Gu, 2012, Acta Pharmacologica Sinica.

Identifying therapeutic biomarkers of zoledronic acid by metabolomics

Xia Li, Zhenlin Zhang, Xiang Yu, 2023, Frontiers in Pharmacology.

Associations of polymorphisms in the SOST gene and bone mineral density in postmenopausal Chinese Women

H. Zhang, H. Yue, W. Hu, 2014, Osteoporosis International.

Associations of serum sclerostin and polymorphisms in the SOST gene with bone mineral density and markers of bone metabolism in postmenopausal Chinese women.

Wei-wei Hu, Yujuan Liu, Zhenlin Zhang, 2014, The Journal of clinical endocrinology and metabolism.

A phase III randomized, double-blind, placebo-controlled trial of the denosumab biosimilar QL1206 in postmenopausal Chinese women with osteoporosis and high fracture risk

Guang Wang, Y. Huo, Han Yang, 2022, Acta Pharmacologica Sinica.

Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta.

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2018, International journal of molecular medicine.

Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2009, Acta Pharmacologica Sinica.

Association of HIVEP3 Gene and Lnc RNA with Femoral Neck Bone Mineral Content and Hip Geometry by Genome-Wide Association Analysis in Chinese People

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2020, International journal of endocrinology.

Polymorphisms in the human ALOX12 and ALOX15 genes are associated with peak bone mineral density in Chinese nuclear families

H. Zhang, Y.-J. Liu, H. Yue, 2012, Osteoporosis International.

ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families

H. Zhang, H. Yue, C. Wang, 2010, International Journal of Obesity.

Association of single nucleotide polymorphism Rs2236518 in PRDM16 gene with BMI in Chinese males

Zhenlin Zhang, Jin-wei He, H. Yue, 2013, Acta Pharmacologica Sinica.

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2016, Molecular medicine reports.

The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of Bone and Mineral Metabolism.

No association of the polymorphisms of the frizzled-related protein gene with peak bone mineral density in Chinese nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2010, BMC Medical Genetics.

Targeted resequencing of phosphorus metabolism‑related genes in 86 patients with hypophosphatemic rickets/osteomalacia.

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2018, International journal of molecular medicine.

Association between myostatin gene polymorphisms and peak BMD variation in Chinese nuclear families

H. Zhang, Maolan Li, Y.-J. Liu, 2007, Osteoporosis International.

Identification of Two Novel Mutations in the PHEX Gene in Chinese Patients with Hypophosphatemic Rickets/Osteomalacia

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2014, PloS one.

Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets

Shan-shan Li, Zhenlin Zhang, Jin-wei He, 2016, International journal of molecular medicine.

Physical performance and life quality in postmenopausal women supplemented with vitamin D: a two-year prospective study

X. Xing, Ling Xu, O. Wang, 2015, Acta Pharmacologica Sinica.

Fibroblast Growth Factor 21 Is Associated With Bone Mineral Density, but not With Bone Turnover Markers and Fractures in Chinese Postmenopausal Women.

Wei-wei Hu, C. Wang, Zhenlin Zhang, 2019, Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry.

Vitamin D pathway gene variation rs3740165 is associated with serological uric acid levels in healthy Chinese women

Wei-wei Hu, C. Wang, Zhenlin Zhang, 2022, Frontiers in Endocrinology.

Establishing Reference Intervals for Bone Turnover Markers in the Healthy Shanghai Population and the Relationship with Bone Mineral Density in Postmenopausal Women

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2013, International journal of endocrinology.

A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A

Zhenlin Zhang, Jin-wei He, H. Yue, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Novel mutations in the SEC24D gene in Chinese families with autosomal recessive osteogenesis imperfecta

H. Zhang, H. Yue, C. Wang, 2017, Osteoporosis International.

Association between Low Density Lipoprotein Receptor- Related Protein 2 Gene Polymorphisms and Bone Mineral Density Variation in Chinese Population

Y. Hu, Zhenlin Zhang, Jin-wei He, 2011 .

W. Liu, Shenmin Zhang, Qifu Li, 2022, Journal of orthopaedic translation.

Association of ALOX15 gene polymorphisms with obesity-related phenotypes in Chinese nuclear families with male offspring

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Acta Pharmacologica Sinica.

A mutation in NOTCH2 gene in a Chinese patient with Hajdu-Cheney syndrome.

Zhenlin Zhang, H. Yue, Hao Zhang, 2013, Joint, bone, spine : revue du rhumatisme.

Polymorphisms in the HOXD4 gene are not associated with peak bone mineral density in Chinese nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2010, Acta Pharmacologica Sinica.

Clinical and Molecular Characterization and Discovery of Novel Genetic Mutations of Chinese Patients with COL2A1-related Dysplasia

Wei-wei Hu, Zhenlin Zhang, H. Yue, 2020, International journal of biological sciences.

Clinical and Genetic Characteristics of Hypophosphatasia in Chinese Adults

Xia Li, Wei-wei Hu, Zhenlin Zhang, 2023, Genes.

ALOX12 polymorphisms are associated with fat mass but not peak bone mineral density in Chinese nuclear families

H. Zhang, Congrong Wang, Jin-wei He, 2010, International Journal of Obesity.

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.

Zhenlin Zhang, Jin-wei He, H. Yue, 2013, Bone.

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta

Wei-wei Hu, Zhenlin Zhang, Jin-wei He, 2016, Molecular medicine reports.

Identification of the mutations in the tissue-nonspecific alkaline phosphatase gene in two Chinese families with hypophosphatasia.

Zhenlin Zhang, H. Yue, Hao Zhang, 2012, Archives of medical research.

Contribution of Myostatin gene polymorphisms to normal variation in lean mass, fat mass and peak BMD in Chinese male offspring

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Acta Pharmacologica Sinica.

No association between LRP5 gene polymorphisms and bone and obesity phenotypes in Chinese male-offspring nuclear families

Zhenlin Zhang, Jin-wei He, H. Yue, 2010, Acta Pharmacologica Sinica.

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2009, Journal of Bone and Mineral Metabolism.

The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: six novel mutations of the CLCN7 gene in twelve osteopetrosis families

Zhenlin Zhang, Jin-wei He, H. Yue, 2012, Journal of Bone and Mineral Metabolism.