JOURNAL OF BONE AND MINERAL RESEARCH

Journal

Identifier:

E090767

ISSN:

0884-0431

Overview

Outputs (42)

A New Familial Sclerosing Bone Dysplasia

Academic Article

A new familial sclerosing bone dysplasia.

Academic Article

A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease

Academic Article

A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease.

Academic Article

A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease

Academic Article

Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss

Academic Article

As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene

Academic Article

Bone Mineral Density Predicts Fractures in Chronic Kidney Disease

Translation

Bone quality in hip fractures and hip osteoarthritis.

Abstract

Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis.

Academic Article

Characterization of Extracellular Vesicles in Osteoporotic Patients Compared to Osteopenic and Healthy Controls

Academic Article

Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patients.

Academic Article

Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis

Academic Article

Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone.

Academic Article

Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.

Academic Article

Comparison of intravenous and intramuscular neridronate regimens for the treatment of paget's disease of bone.

Academic Article

In Vitro Differentiation of CD14 Cells From Osteopetrotic Subjects: Contrasting Phenotypes With TCIRG1, CLCN7, and Attachment Defects.

Academic Article

Increased Risk of Bone Fractures in Hemodialysis Patients Treated with Proton Pump Inhibitors in Real World: Results from the Dialysis Outcomes and Practice Patterns Study (DOPPS)

Academic Article

Klotho Variants and Chronic Hemodialysis Mortality.

Academic Article

Large Collaborative Study on Geographic Variation of SQSTM1 Mutations in Paget's Disease of Bone in Italy

Conference Paper

Muscle microstructure: a new point of view on osteoporosis-related muscle atrophy.

Conference Paper

Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement.

Academic Article

Oral Calcitriol Use, Vertebral Fractures, and Vitamin K in Hemodialysis Patients: A Cross-Sectional Study

Academic Article

Osteopetrosis rescue upon RANKL administration to Rankl -/- mice: A new therapy for human RANKL-dependent ARO

Academic Article

Overexpression of Deaminase Acting on RNA-2 enzyme ADAR2 Reduces Osteosarcoma Progression

Abstract

Pathobiologic Mechanisms of Neurodegeneration in Osteopetrosis Derived from Structural and Functional Analysis of 14 ClC-7 Mutants

Academic Article

Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women.

Academic Article

RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations.

Academic Article

Relationship Between Low Bone Mineral Density and Fractures With Incident Cardiovascular Disease: A Systematic Review and Meta-Analysis

Academic Article

Romosozumab Use and Cardiovascular Events

Academic Article

SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.

Academic Article

SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone

Academic Article

Sclerostin Regulation, Microarchitecture, and Advanced Glycation End-Products in the Bone of Elderly Women With Type 2 Diabetes

Academic Article

Sevelamer Use, Vitamin K Levels, Vascular Calcifications, and Vertebral Fractures in Hemodialysis Patients: Results from the VIKI Study

Academic Article

Severe Malignant Osteopetrosis Caused by a GL Gene Mutation.

Academic Article

Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis.

Academic Article

Transfer, analysis and reversion of the fibrous dysplasia cellular phenotype in human skeletal progenitors

Academic Article

Urokinase plasminogen activator receptor affects bone homeostasis by regulating osteoblast and osteoclast

Academic Article

Vitamin D Receptor (VDR) gene polymorphism is associated with Left Ventricular (LV) mass and predicts Left Ventricular Hypertrophy (LVH) progression in End-Stage Renal Disease (ESRD) patients

Academic Article

Vitamin K, vertebral fractures, vascular calcifications and mortality: Vitamin K Italian (VIKI) dialysis study.

Academic Article

Vitamin K, vertebral fractures, vascular calcifications, and mortality: VItamin K Italian (VIKI) dialysis study.

Academic Article

ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology

Academic Article

No Results Found

JOURNAL OF BONE AND MINERAL RESEARCH

Overview

Outputs (42)