Pathogenesis of Paget disease of bone. (Q38006389)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

title

Pathogenesis of Paget disease of bone (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

1

Stuart H Ralston

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

language of work or name

English

0 references

publication date

29 April 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

Calcified Tissue International

30 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

volume

91

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

30 January 2020

page(s)

97-113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

The p62 P392L mutation linked to Paget's disease induces activation of human osteoclasts

30 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Pathogenesis of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The epidemiology of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Incidence and natural history of Paget's disease of bone in England and Wales.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Archaeological skeletons support a northwest European origin for Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease in New Zealand: evidence for declining prevalence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Epidemiology of Paget's disease in Europe: the prevalence is decreasing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease of bone in New Zealand: continued decline in disease severity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Prevalence of Paget's disease of bone in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Long-term trends in the incidence of Paget's disease of bone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease of bone in Lancashire and arsenic pesticide in cotton mill wastewater: a speculative hypothesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease in a treadle machine operator

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Characteristics and familial aggregation of Paget's disease of bone in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Cattle, pets, and Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Past pets and Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Multicenter blinded analysis of RT-PCR detection methods for paramyxoviruses in relation to Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The pro and con of measles virus in Paget's disease: con.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Randomized trial of intensive bisphosphonate treatment versus symptomatic management in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Clinical determinants of quality of life in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paramyxovirus-like nuclear inclusions identical to those of Paget's disease of bone detected in giant cells of primary oxalosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Huntington's disease intranuclear inclusions contain truncated, ubiquitinated huntingtin protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Osteoclast differentiation from circulating mononuclear precursors in Paget's disease is hypersensitive to 1,25-dihydroxyvitamin D(3) and RANKL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Interleukin 6. A potential autocrine/paracrine factor in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

FGF-2 stimulation of RANK ligand expression in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Dickkopf-1 as a potential therapeutic target in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The atypical PKC-interacting protein p62 is an important mediator of RANK-activated osteoclastogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Deubiquitinating enzyme CYLD negatively regulates RANK signaling and osteoclastogenesis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Mutant p62P392L Stimulation of Osteoclast Differentiation in Paget's Disease of Bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Bone stromal cells in pagetic bone and Paget's sarcoma express RANKL and support human osteoclast formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Frequency and characteristics of familial aggregation of paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Familial Paget's disease in The Netherlands: occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Familial aggregation of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

A family study of Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

SQSTM1 and Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Macrophage colony-stimulating factor is indispensable for both proliferation and differentiation of osteoclast progenitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: Evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondral ossification

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

RANK is the intrinsic hematopoietic cell surface receptor that controls osteoclastogenesis and regulation of bone mass and calcium metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Genetic linkage of familial expansile osteolysis to chromosome 18q

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Phenotypic characterization of early onset Paget's disease of bone caused by a 27-bp duplication in the TNFRSF11A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Expansile skeletal hyperphosphatasia: a new familial metabolic bone disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Signal peptide mutations in RANK prevent downstream activation of NF-κB.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Evaluation of the role of RANK and OPG genes in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Optineurin negatively regulates TNFalpha- induced NF-kappaB activation by competing with NEMO for ubiquitinated RIP

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Phosphorylation of the autophagy receptor optineurin restricts Salmonella growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Adult-onset primary open-angle glaucoma caused by mutations in optineurin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Mutations of optineurin in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Optineurin is required for CYLD-dependent inhibition of TNFα-induced NF-κB activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Osteoprotegerin deficiency and juvenile Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Deletion of aspartate 182 in OPG causes juvenile Paget's disease by impairing both protein secretion and binding to RANKL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Identification of sex-specific associations between polymorphisms of the osteoprotegerin gene, TNFRSF11B, and Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Nup93, a Vertebrate Homologue of Yeast Nic96p, Forms a Complex with a Novel 205-kDa Protein and Is Required for Correct Nuclear Pore Assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The role of PML in tumor suppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The Ubx2 and Ubx3 cofactors direct Cdc48 activity to proteolytic and nonproteolytic ubiquitin-dependent processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

AAA ATPase p97/valosin-containing protein interacts with gp78, a ubiquitin ligase for endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Targeted deletion of p97 (VCP/CDC48) in mouse results in early embryonic lethality.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Endolysosomal sorting of ubiquitylated caveolin-1 is regulated by VCP and UBXD1 and impaired by VCP disease mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Somatic mutations in SQSTM1 detected in affected tissues from patients with sporadic Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Recent advances in understanding the molecular basis of Paget disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Regulation of mammalian autophagy in physiology and pathophysiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Ubiquitin signals autophagic degradation of cytosolic proteins and peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Neighbor of Brca1 gene (Nbr1) functions as a negative regulator of postnatal osteoblastic bone formation and p38 MAPK activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

NBR1 cooperates with p62 in selective autophagy of ubiquitinated targets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease of bone in the French population: novel SQSTM1 mutations, functional analysis, and genotype-phenotype correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Autophagy proteins regulate the secretory component of osteoclastic bone resorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Nuclear inclusions in Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Multinucleated cells formed in vitro from Paget's bone marrow express viral antigens

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Bone tissue in Paget's disease of bone. Ultrastructure and Immunocytology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Immunohistological demonstration of respiratory syncytial virus antigens in Paget disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Paget's disease of bone and previous pet ownership in the United States: dogs exonerated

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Canine distemper virus localised in bone cells of patients with Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Detection of canine distemper virus in 100% of Paget's disease samples by in situ-reverse transcriptase-polymerase chain reaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Canine distemper virus transcripts sequenced from pagetic bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Measles virus RNA detected in Paget's disease bone tissue by in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Measles virus nucleocapsid transcript expression is not restricted to the osteoclast lineage in patients with Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Failure to detect paramyxovirus sequences in Paget's disease of bone using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Absence of measles virus and canine distemper virus transcripts in long-term bone marrow cultures from patients with Paget's disease of bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Sequence analysis of measles virus nucleocapsid transcripts in patients with Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Failure to detect measles virus ribonucleic acid in bone cells from patients with Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Generation of multinucleated osteoclast-like cells from canine bone marrow: Effects of canine distemper virus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Osteoclasts formed by measles virus-infected osteoclast precursors from hCD46 transgenic mice express characteristics of pagetic osteoclasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Osteoclasts expressing the measles virus nucleocapsid gene display a pagetic phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Contributions of the measles virus nucleocapsid gene and the SQSTM1/p62(P392L) mutation to Paget's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Expression of measles virus nucleocapsid protein in osteoclasts induces Paget's disease-like bone lesions in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Mice transgenic for HTLV-I LTR-tax exhibit tax expression in bone, skeletal alterations, and high bone turnover.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

A SQSTM1/p62 mutation linked to Paget's disease increases the osteoclastogenic potential of the bone microenvironment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

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-kappaB signaling without loss of ubiquitin binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Three Novel Mutations in SQSTM1 Identified in Familial Paget's Disease of Bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Two novel mutations at exon 8 of the Sequestosome 1 (SQSTM1) gene in an Italian series of patients affected by Paget's disease of bone (PDB).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

RANKL maintains bone homeostasis through c-Fos-dependent induction of interferon-β

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Mutation Screening of the TNFRSF11A Gene Encoding Receptor Activator of NFkB (RANK) in Familial and Sporadic Paget's Disease of Bone and Osteosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

A Negative Search for a Paramyxoviral Etiology of Paget's Disease of Bone: Molecular, Immunological, and Ultrastructural Studies in U.K. Patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

Loss of Ubiquitin Binding Is a Unifying Mechanism by Which Mutations of SQSTM1 Cause Paget’s Disease of Bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S00223-012-9599-0

10.1007/S00223-012-9599-0

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json

Dimensions Publication ID

30 January 2020

1038411294

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22543925 AND SRC:MED&resulttype=core&format=json