Wei-wei Hu

发表

Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent‐1 disease

Zhenlin Zhang, Jin-wei He, H. Yue, 2014, Nephrology.

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.

Age-related changes of serum tartrate-resistant acid phosphatase 5b and the relationship with bone mineral density in Chinese women

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2008, Acta Pharmacologica Sinica.

The duration of beta‐blocker therapy and outcomes in patients without heart failure or left ventricular systolic dysfunction after acute myocardial infarction: A multicenter prospective cohort study

Dong-Ying Zhang, Qin Duan, S. Qin, 2022, Clinical cardiology.

Serum osteocalcin levels are inversely associated with plasma glucose and body mass index in healthy Chinese women

Di Chen, Zhenlin Zhang, Jin-wei He, 2014, Acta Pharmacologica Sinica.

An Ac transposon system based on maize chromosome 4S for isolating long-distance-transposed Ac tags in the maize genome

Gang Wang, Fei Wang, Zhengkai Xu, 2010, Genetica.

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.

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.

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.

[Osteoprotegerin gene polymorphism and therapeutic response to alendronate in postmenopausal women with osteoporosis].

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2009, Zhonghua yi xue za zhi.

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.

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.

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.

Association between SNP and haplotypes in PPARGC1 and adiponectin genes and bone mineral density in Chinese nuclear families

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2007, Acta Pharmacologica Sinica.

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.

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.

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.

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

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

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.

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 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.

Contribution of the sclerostin domain-containing protein 1 (SOSTDC1) gene to normal variation of peak bone mineral density in Chinese women and men

Zhenlin Zhang, Jin-wei He, H. Yue, 2011, Journal of Bone and Mineral Metabolism.

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.

The efficacy and safety of weekly 35-mg risedronate dosing regimen for Chinese postmenopausal women with osteoporosis or osteopenia: 1-year data

W. Xia, Zhenlin Zhang, Jin-wei He, 2015, 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.

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.

Bone mineral density of the spine and femur in healthy Chinese men.

Zhenlin Zhang, Jin-wei He, Hao Zhang, 2006, Asian journal of andrology.

Identifying therapeutic biomarkers of zoledronic acid by metabolomics

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

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.

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 .

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.

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.

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 myostatin gene polymorphisms and peak BMD variation in Chinese nuclear families

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