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Targeting loop3 of sclerostin preserves its cardiovascular protective action and promotes bone formation

Nature communications, 2022-07, Vol.13 (1), p.4241-4241, Article 4241

2022

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Oxygen content-related DNA damage of graphene oxide on human retinal pigment epithelium cells

Journal of materials science. Materials in medicine, 2021-02, Vol.32 (2), p.20-20, Article 20

2021

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Nonremission and Recurrent Tumor‐Induced Osteomalacia: A Retrospective Study

Journal of bone and mineral research, 2020-03, Vol.35 (3), p.469-477

2020

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Pharmacological Treatment of Bone Loss

Current pharmaceutical design, 2017-01, Vol.23 (41), p.6298

2017

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Recurrent Femoral Fractures in a Boy with an Atypical Progeroid Syndrome: A Case Report

Calcified tissue international, 2020-03, Vol.106 (3), p.325-330

2020

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Novel 4.18 Mb deletion resulting in 2q37 microdeletion syndrome combined with PTH resistance found in one Chinese patient

Endocrine, 2024-02, Vol.85 (1), p.331-340

2024

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Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification

Orphanet journal of rare diseases, 2023-08, Vol.18 (1), p.234-234, Article 234

2023

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Correction to: Oxygen content-related DNA damage of graphene oxide on human retinal pigment epithelium cells

Journal of materials science. Materials in medicine, 2022-02, Vol.33 (2), p.23-23, Article 23

2022

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An adult patient of X-linked hypophosphatemia with joint manifestation mimicking spondylarthritis

Chinese medical journal, 2022-05, Vol.135 (10), p.1255-1257

2022

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Age‐, Site‐, and Sex‐Specific Normative Centile Curves for HR‐pQCT‐Derived Microarchitectural and Bone Strength Parameters in a Chinese Mainland Population

Journal of bone and mineral research, 2020-11, Vol.35 (11), p.2159-2170

2020

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Clinical, Biochemical, Radiological, and Genetic Analyses of a Patient with VCP Gene Variant-Induced Paget’s Disease of Bone

Calcified tissue international, 2022-04, Vol.110 (4), p.518-528

2022

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Bone mineral density and microarchitecture among Chinese patients with rheumatoid arthritis: a cross-sectional study with HRpQCT

Arthritis research & therapy, 2021-04, Vol.23 (1), p.127-127, Article 127

2021

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Clinical Characteristics and Bone Features of Autosomal Recessive Hypophosphatemic Rickets Type 1 in Three Chinese Families: Report of Five Chinese Cases and Review of the Literature

Calcified tissue international, 2020-12, Vol.107 (6), p.636-648

2020

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Locoregional recurrence of parathyroid carcinoma: how to identify this rare but fatal condition using ultrasonography

Endocrine Journal, 2021, Vol.68(10), pp.1179-1186

2021

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A novel long-range deletion spanning STX16 and NPEPL1 causing imprinting defects of the GNAS locus discovered in a patient with autosomal-dominant pseudohypoparathyroidism type 1B

Endocrine, 2020-07, Vol.69 (1), p.212-219

2020

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Full-length versus intact PTH concentrations in pseudohypoparathyroidism type 1 and primary hyperparathyroidism: clinical evaluation of immunoassays in individuals from China

Endocrine, 2022-12, Vol.78 (3), p.605-614

2022

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Optimization of Neferine Purification Based on Response Surface Methodology and Its Anti-Metastasis Mechanism on HepG2 Cells

Molecules (Basel, Switzerland), 2023-06, Vol.28 (13), p.5086

2023

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Association of serum osteocalcin with bone microarchitecture and muscle mass in Beijing community-dwelling postmenopausal women

Endocrine, 2024-04, Vol.84 (1), p.236-244

2024

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Explorative research on glucolipid metabolism and levels of adipokines in pseudohypoparathyroidism type 1 patients

Orphanet journal of rare diseases, 2023-11, Vol.18 (1), p.1-367, Article 367

2023

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Successful treatment of tumor-induced osteomalacia causing by phosphaturic mesenchymal tumor of the foot

Medicine (Baltimore), 2019-07, Vol.98 (27), p.e16296-e16296

2019

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Comparison of differences in bone microarchitecture in adult- versus juvenile-onset type 1 diabetes Asian males versus non-diabetes males: an observational cross-sectional pilot study

Endocrine, 2021-01, Vol.71 (1), p.87-95

2021

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Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

American journal of human genetics, 2012-01, Vol.90 (1), p.125-132

2012

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A novel long-range deletion spanning CDC73 and upper-stream genes discovered in a kindred of familial primary hyperparathyroidism

Endocrine, 2022-03, Vol.75 (3), p.907-915

2022

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Preoperative evaluation and orthopedic surgical strategies for tumor-induced osteomalacia

Journal of bone oncology, 2024-04, Vol.45, p.100600-100600, Article 100600

2024

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Health-related quality of life in men with osteoporosis: a systematic review and meta-analysis

Endocrine, 2021-11, Vol.74 (2), p.270-280

2021

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Targeting loop3 of sclerostin preserves its cardiovascular protective action and promotes bone formation

Oxygen content-related DNA damage of graphene oxide on human retinal pigment epithelium cells

Nonremission and Recurrent Tumor‐Induced Osteomalacia: A Retrospective Study

Pharmacological Treatment of Bone Loss

Recurrent Femoral Fractures in a Boy with an Atypical Progeroid Syndrome: A Case Report

Novel 4.18 Mb deletion resulting in 2q37 microdeletion syndrome combined with PTH resistance found in one Chinese patient

Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification

Correction to: Oxygen content-related DNA damage of graphene oxide on human retinal pigment epithelium cells

An adult patient of X-linked hypophosphatemia with joint manifestation mimicking spondylarthritis

Age‐, Site‐, and Sex‐Specific Normative Centile Curves for HR‐pQCT‐Derived Microarchitectural and Bone Strength Parameters in a Chinese Mainland Population

Clinical, Biochemical, Radiological, and Genetic Analyses of a Patient with VCP Gene Variant-Induced Paget’s Disease of Bone

Bone mineral density and microarchitecture among Chinese patients with rheumatoid arthritis: a cross-sectional study with HRpQCT

Clinical Characteristics and Bone Features of Autosomal Recessive Hypophosphatemic Rickets Type 1 in Three Chinese Families: Report of Five Chinese Cases and Review of the Literature

Locoregional recurrence of parathyroid carcinoma: how to identify this rare but fatal condition using ultrasonography

A novel long-range deletion spanning STX16 and NPEPL1 causing imprinting defects of the GNAS locus discovered in a patient with autosomal-dominant pseudohypoparathyroidism type 1B

Full-length versus intact PTH concentrations in pseudohypoparathyroidism type 1 and primary hyperparathyroidism: clinical evaluation of immunoassays in individuals from China

Optimization of Neferine Purification Based on Response Surface Methodology and Its Anti-Metastasis Mechanism on HepG2 Cells

Association of serum osteocalcin with bone microarchitecture and muscle mass in Beijing community-dwelling postmenopausal women

Explorative research on glucolipid metabolism and levels of adipokines in pseudohypoparathyroidism type 1 patients

Successful treatment of tumor-induced osteomalacia causing by phosphaturic mesenchymal tumor of the foot

Comparison of differences in bone microarchitecture in adult- versus juvenile-onset type 1 diabetes Asian males versus non-diabetes males: an observational cross-sectional pilot study

Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

A novel long-range deletion spanning CDC73 and upper-stream genes discovered in a kindred of familial primary hyperparathyroidism

Preoperative evaluation and orthopedic surgical strategies for tumor-induced osteomalacia

Health-related quality of life in men with osteoporosis: a systematic review and meta-analysis

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