Jie-mei Gu

发表

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.

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.

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

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.

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.

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.

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.

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 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.

Une mutation dans le gène NOTCH2 chez un patient chinois porteur d’un syndrome de Hadju-Cheney☆

Jie-mei Gu, Yunhua Hu, Hao Zhang, 2013 .

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.