New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis. (Q37748586)

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scientific article published on 11 May 2010

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English	New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis.	scientific article published on 11 May 2010

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2 February 2020

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New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis (English)

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2 February 2020

Derek Anthony Scott

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J C Crockett

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D J Mellis

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M H Helfrich

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Osteoporosis International

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2 February 2020

Intracranial calcification in children with osteopetrosis caused by carbonic anhydrase II deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS00198-010-1272-8

21 January 2018

Crystal structure of the TRANCE/RANKL cytokine reveals determinants of receptor-ligand specificity

1 reference

https://api.crossref.org/works/10.1007%2FS00198-010-1272-8

21 January 2018

Paget disease of bone

1 reference

https://api.crossref.org/works/10.1007%2FS00198-010-1272-8

21 January 2018

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

1 reference

https://api.crossref.org/works/10.1007%2FS00198-010-1272-8

21 January 2018

Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Applying nonsense-mediated mRNA decay research to the clinic: progress and challenges

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: report of 20 novel mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paget's disease of bone--becoming a rarity?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hematopoietic stem cell transplantation for osteopetrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ubiquitin signalling in the NF-kappaB pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Commitment and differentiation of osteoclast precursor cells by the sequential expression of c-Fms and receptor activator of nuclear factor kappaB (RANK) receptors

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoprotegerin: a novel secreted protein involved in the regulation of bone density

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of understanding of genetics of Paget's disease of bone and related diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GM-CSF and IL-4 induce dendritic cell differentiation and disrupt osteoclastogenesis through M-CSF receptor shedding by up-regulation of TNF-alpha converting enzyme (TACE).

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spleen Cells Transmit Osteopetrosis in Mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced expression and shedding of receptor activator of NF-kappaB ligand during tumor-bone interaction potentiates mammary tumor-induced osteolysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Canonical and non-canonical pathways of osteoclast formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone Resorption Restored in Osteopetrotic Mice by Transplants of Normal Bone Marrow and Spleen Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonproteolytic functions of ubiquitin in cell signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential Gene Expression in Cultured Osteoblasts and Bone Marrow Stromal Cells From Patients With Paget's Disease of Bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of Ubiquitin-Binding Associated With Paget's Disease of Bone p62 (SQSTM1) Mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile malignant, autosomal recessive osteopetrosis: the rich and the poor

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three is better than one: pre-ligand receptor assembly in the regulation of TNF receptor signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A domain in TNF receptors that mediates ligand-independent receptor assembly and signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Removal of osteoclast bone resorption products by transcytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoclasts: what do they do and how do they do it?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial expansile osteolysis. A new dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new heterozygous mutation (R714C) of the osteopetrosis gene, pleckstrin homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP secretion in osteoclasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial expansile osteolysis (excessive RANK effect) in a 5-generation American kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Receptor activator of NF-kappaB (RANK) ligand induces ectodomain shedding of RANK in murine RAW264.7 macrophages.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of Cbl-b increases osteoclast bone-resorbing activity and induces osteopenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autophagy, organelles and ageing

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics and aetiology of Pagetic disorders of bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formation of stacked ER cisternae by low affinity protein interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Receptor activator of NF-kappaB ligand (RANKL) activates TAK1 mitogen-activated protein kinase kinase kinase through a signaling complex containing RANK, TAB2, and TRAF6

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe liver degeneration and lack of NF-kappaB activation in NEMO/IKKgamma-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic characteristics of bone in carbonic anhydrase II-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a role of a tumor necrosis factor-alpha (TNF-alpha)-converting enzyme-like protease in shedding of TRANCE, a TNF family member involved in osteoclastogenesis and dendritic cell survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atp6i-deficient mice exhibit severe osteopetrosis due to loss of osteoclast-mediated extracellular acidification.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trafficking of Matrix Collagens Through Bone-Resorbing Osteoclasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ubiquitin-mediated signalling and Paget's disease of bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TAK1-dependent signaling requires functional interaction with TAB2/TAB3

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MMP-7 promotes prostate cancer-induced osteolysis via the solubilization of RANKL.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital osteopetrotic mutations as probes of the origin, structure, and function of osteoclasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoclast biology: lessons from mammalian mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoprotegerin deficiency and juvenile Paget's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Signal transduction from the endoplasmic reticulum to the cell nucleus

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of the sequestosome 1 (p62) gene increases osteoclastogenesis but does not induce Paget disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TRAF6 ubiquitin ligase is essential for RANKL signaling and osteoclast differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RANK is essential for osteoclast and lymph node development

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Type II autosomal dominant osteopetrosis (Albers-Schönberg disease): clinical and radiological manifestations in 42 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteopetrosis cured by temporary parabiosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Central control of fever and female body temperature by RANKL/RANK

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensing of Lys 63-linked polyubiquitination by NEMO is a key event in NF-kappaB activation [corrected]

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensive clear zone and defective ruffled border formation in osteoclasts of osteopetrotic (ia/ia) rats: implications for secretory function

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenesis and management of Paget's disease of bone.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autophagy counterbalances endoplasmic reticulum expansion during the unfolded protein response

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Self-assembled RANK induces osteoclastogenesis ligand-independently.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel receptor activator of NF-kappaB (RANK) cytoplasmic motif plays an essential role in osteoclastogenesis by committing macrophages to the osteoclast lineage

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of NF-kappaB by RANK requires tumor necrosis factor receptor-associated factor (TRAF) 6 and NF-kappaB-inducing kinase. Identification of a novel TRAF6 interaction motif

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in TRAF6-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansile skeletal hyperphosphatasia is caused by a 15-base pair tandem duplication in TNFRSF11A encoding RANK and is allelic to familial expansile osteolysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role(s) of Src kinase and Cbl proteins in the regulation of osteoclast differentiation and function

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

One step at a time: endoplasmic reticulum-associated degradation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A positive regulatory role for Cbl family proteins in tumor necrosis factor-related activation-induced cytokine (trance) and CD40L-mediated Akt activation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of Somatic SQSTM1 Mutations in Paget’s Disease of Bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, genetic, and cellular analysis of 49 osteopetrotic patients: implications for diagnosis and treatment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RANK/RANKL: regulators of immune responses and bone physiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Cl-/H+ antiporter ClC-7 is the primary chloride permeation pathway in lysosomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Shared principles in NF-kappaB signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interactions of tumor necrosis factor (TNF) and TNF receptor family members in the mouse and human

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse osteopetrotic grey-lethal mutation induces a defect in osteoclast maturation/function.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile Paget's disease, familial expansile osteolysis and other genetic osteolytic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines on the management of Paget's disease of bone

1 reference

https://pubmed.ncbi.nlm.nih.gov/20458572

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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