Journal of bone and mineral research

Label

• Journal of bone and mineral research (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patients. (Articolo in rivista) (Prodotto della ricerca)
• Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene (Articolo in rivista) (Prodotto della ricerca)
• RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Large Collaborative Study on Geographic Variation of SQSTM1 Mutations in Paget's Disease of Bone in Italy (Contributo in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1301)
• SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone (Articolo in rivista) (Prodotto della ricerca)
• Comparison of intravenous and intramuscular neridronate regimens for the treatment of paget's disease of bone. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Transfer, analysis and reversion of the fibrous dysplasia cellular phenotype in human skeletal progenitors (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Vitamin K, vertebral fractures, vascular calcifications, and mortality: VItamin K Italian (VIKI) dialysis study. (Articolo in rivista) (Prodotto della ricerca)
• SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. (Articolo in rivista) (Prodotto della ricerca)
• A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (Prodotto della ricerca)
• Severe Malignant Osteopetrosis Caused by a GL Gene Mutation. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Vitamin K, vertebral fractures, vascular calcifications and mortality: Vitamin K Italian (VIKI) dialysis study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Osteopetrosis rescue upon RANKL administration to Rankl -/- mice: A new therapy for human RANKL-dependent ARO (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women. (Articolo in rivista) (Prodotto della ricerca)
• Vitamin D Receptor (VDR) Gene Polymorphism is associated with Left Ventricular (LV) Mass and predicts LVH progression in end stage renal disease (ESRD) patients. (Articolo in rivista) (Prodotto della ricerca)
• 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. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone. (Articolo in rivista) (Prodotto della ricerca)
• A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. (Articolo in rivista) (Prodotto della ricerca)
• A new familial sclerosing bone dysplasia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Urokinase plasminogen activator receptor affects bone homeostasis by regulating osteoblast and osteoclast (Articolo in rivista) (Prodotto della ricerca)
• In Vitro Differentiation of CD14 Cells From Osteopetrotic Subjects: Contrasting Phenotypes With TCIRG1, CLCN7, and Attachment Defects. (Articolo in rivista) (Prodotto della ricerca)
• Klotho Variants and Chronic Hemodialysis Mortality. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)

Alternative label

• JBMR (literal)
• J. bone miner. res. (literal)
• Journal of bone and mineral research (literal)

Language

• eng (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn

• 0884-0431 (literal)

Preferred label

• Journal of bone and mineral research (literal)

Publisher

• Mary Ann Liebert, New York : USA (literal)

Incoming links:

Rivista

• Large Collaborative Study on Geographic Variation of SQSTM1 Mutations in Paget's Disease of Bone in Italy (Contributo in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1301)
• Klotho Variants and Chronic Hemodialysis Mortality. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Urokinase plasminogen activator receptor affects bone homeostasis by regulating osteoblast and osteoclast (Articolo in rivista) (Prodotto della ricerca)
• Transfer, analysis and reversion of the fibrous dysplasia cellular phenotype in human skeletal progenitors (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• 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. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Vitamin D Receptor (VDR) Gene Polymorphism is associated with Left Ventricular (LV) Mass and predicts LVH progression in end stage renal disease (ESRD) patients. (Articolo in rivista) (Prodotto della ricerca)
• A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone (Articolo in rivista) (Prodotto della ricerca)
• Comparison of intravenous and intramuscular neridronate regimens for the treatment of paget's disease of bone. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women. (Articolo in rivista) (Prodotto della ricerca)
• In Vitro Differentiation of CD14 Cells From Osteopetrotic Subjects: Contrasting Phenotypes With TCIRG1, CLCN7, and Attachment Defects. (Articolo in rivista) (Prodotto della ricerca)
• Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Severe Malignant Osteopetrosis Caused by a GL Gene Mutation. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A new familial sclerosing bone dysplasia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Osteopetrosis rescue upon RANKL administration to Rankl -/- mice: A new therapy for human RANKL-dependent ARO (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Characterization of a novel Alu-Alu recombination-mediated genomic deletion in the TCIRG1 gene in five osteopetrotic patients. (Articolo in rivista) (Prodotto della ricerca)
• Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. (Articolo in rivista) (Prodotto della ricerca)
• RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Vitamin K, vertebral fractures, vascular calcifications and mortality: Vitamin K Italian (VIKI) dialysis study. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Vitamin K, vertebral fractures, vascular calcifications, and mortality: VItamin K Italian (VIKI) dialysis study. (Articolo in rivista) (Prodotto della ricerca)
• Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. (Articolo in rivista) (Prodotto della ricerca)
• As little as needed: The extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene (Articolo in rivista) (Prodotto della ricerca)
• A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Clinical characteristics and evolution of giant cell tumor occurring in paget's disease of bone. (Articolo in rivista) (Prodotto della ricerca)
• A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (Prodotto della ricerca)