标题
Pathogenesis of Paget Disease of Bone
作者
关键词
-
出版物
CALCIFIED TISSUE INTERNATIONAL
Volume 91, Issue 2, Pages 97-113
出版商
Springer Nature
发表日期
2012-04-28
DOI
10.1007/s00223-012-9599-0
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Lysine 63-linked polyubiquitin potentially partners with p62 to promote the clearance of protein inclusions by autophagy
- (2014) Jeanne M.M Tan et al. Autophagy
- Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system
- (2012) Hemmo Meyer et al. NATURE CELL BIOLOGY
- Contributions of the Measles Virus Nucleocapsid Gene and the SQSTM1/p62P392L Mutation to Paget's Disease
- (2011) Noriyoshi Kurihara et al. Cell Metabolism
- Autophagy Proteins Regulate the Secretory Component of Osteoclastic Bone Resorption
- (2011) Carl J. DeSelm et al. DEVELOPMENTAL CELL
- Mutant p62P392LStimulation of Osteoclast Differentiation in Paget's Disease of Bone
- (2011) Kumaran Sundaram et al. ENDOCRINOLOGY
- A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice
- (2011) Anna Daroszewska et al. HUMAN MOLECULAR GENETICS
- Signal peptide mutations in RANK prevent downstream activation of NF-κB
- (2011) Julie C Crockett et al. JOURNAL OF BONE AND MINERAL RESEARCH
- A nonsynonymousTNFRSF11Avariation increases NFκB activity and the severity of Paget's disease
- (2011) Fernando Gianfrancesco et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms
- (2011) Pui Yan Jenny Chung et al. MOLECULAR GENETICS AND METABOLISM
- Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations
- (2011) Danilo Ritz et al. NATURE CELL BIOLOGY
- Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
- (2011) Omar M E Albagha et al. NATURE GENETICS
- Optineurin Is Required for CYLD-Dependent Inhibition of TNFα-Induced NF-κB Activation
- (2011) Ananthamurthy Nagabhushana et al. PLoS One
- Phosphorylation of the Autophagy Receptor Optineurin Restricts Salmonella Growth
- (2011) P. Wild et al. SCIENCE
- VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD
- (2010) Emilie Tresse et al. Autophagy
- Dickkopf-1 as a potential therapeutic target in Paget's disease of bone
- (2010) Helen S McCarthy et al. EXPERT OPINION ON THERAPEUTIC TARGETS
- Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone
- (2010) Sara K. Custer et al. HUMAN MOLECULAR GENETICS
- Osteoclasts in human osteopetrosis contain viral-nucleocapsid-like nuclear inclusions
- (2010) Barbara G. Mills et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Absence of paramyxovirus RNA in cultures of pagetic bone cells and in pagetic bon
- (2010) M.A. Birch et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Macrophage colony-stimulating factor restores bone resorption in op/op bone in vitro in conjunction with parathyroid hormone or 1,25-dihydroxyvitamin D3
- (2010) Tomio Morohashi et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Failure to detect paramyxovirus sequences in paget's disease of bone using the polymerase chain reaction
- (2010) Stuart H. Ralston et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Frequency and characteristics of familial aggregation of paget's disease of bone
- (2010) A.A. Morales-Piga et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Familial aggregation of paget's disease of bone
- (2010) Ethel S. Siris et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Archaeological skeletons support a northwest European origin for Paget's disease of bone
- (2010) Simon Mays JOURNAL OF BONE AND MINERAL RESEARCH
- Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone
- (2010) Pui Yan Jenny Chung et al. JOURNAL OF BONE AND MINERAL RESEARCH
- SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone
- (2010) Luigi Gennari et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Mutations ofSQSTM1are associated with severity and clinical outcome in paget disease of bone
- (2010) Micaela Rios Visconti et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Mutations of optineurin in amyotrophic lateral sclerosis
- (2010) Hirofumi Maruyama et al. NATURE
- Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
- (2010) Omar M E Albagha et al. NATURE GENETICS
- Regulation of Mammalian Autophagy in Physiology and Pathophysiology
- (2010) Brinda Ravikumar et al. PHYSIOLOGICAL REVIEWS
- VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease
- (2010) Mallikarjun Badadani et al. PLoS One
- Neighbor of Brca1 gene (Nbr1) functions as a negative regulator of postnatal osteoblastic bone formation and p38 MAPK activity
- (2010) C. A. Whitehouse et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- NBR1 co-operates with p62 in selective autophagy of ubiquitinated targets
- (2009) Vladimir Kirkin et al. Autophagy
- Sequestosome 1 Mutations in Paget's Disease of Bone in Australia: Prevalence, Genotype/Phenotype Correlation, and a Novel Non-UBA Domain Mutation (P364S) Associated With Increased NF-κB Signaling Without Loss of Ubiquitin Binding
- (2009) Sarah L Rea et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Randomized trial of intensive bisphosphonate treatment versus symptomatic management in paget's disease of bone
- (2009) Anne L Langston et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease
- (2009) Jeong-Sun Ju et al. JOURNAL OF CELL BIOLOGY
- Recent advances in understanding the molecular basis of Paget disease of bone
- (2009) A Goode et al. JOURNAL OF CLINICAL PATHOLOGY
- FGF-2 Stimulation of RANK Ligand Expression in Paget’s Disease of Bone
- (2009) Kumaran Sundaram et al. MOLECULAR ENDOCRINOLOGY
- The p62 P392L Mutation Linked to Paget’s Disease Induces Activation of Human Osteoclasts
- (2009) Estelle Chamoux et al. MOLECULAR ENDOCRINOLOGY
- Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
- (2008) Virginia. E. Kimonis et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Pathogenesis of Paget's disease of bone
- (2008) Stuart H. Ralston BONE
- Genetic Epidemiology of Paget’s Disease of Bone in Italy: sequestosome1/p62 Gene Mutational Test and Haplotype Analysis at 5q35 in a Large Representative Series of Sporadic and Familial Italian Cases of Paget’s Disease of Bone
- (2008) Alberto Falchetti et al. CALCIFIED TISSUE INTERNATIONAL
- A SQSTM1/p62 mutation linked to Paget’s disease increases the osteoclastogenic potential of the bone microenvironment
- (2008) Yuko Hiruma et al. HUMAN MOLECULAR GENETICS
- Somatic Mutations inSQSTM1Detected in Affected Tissues From Patients With Sporadic Paget's Disease of Bone
- (2008) Anand Merchant et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Failure to Detect Measles Virus Ribonucleic Acid in Bone Cells from Patients with Paget’s Disease
- (2008) Brya G. Matthews et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Absence of Somatic SQSTM1 Mutations in Paget’s Disease of Bone
- (2008) Brya G. Matthews et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Deubiquitinating enzyme CYLD negatively regulates RANK signaling and osteoclastogenesis in mice
- (2008) Wei Jin et al. JOURNAL OF CLINICAL INVESTIGATION
- Ubiquitin signals autophagic degradation of cytosolic proteins and peroxisomes
- (2008) P. K. Kim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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