Characterization of osteoclasts from patients harboring a G215R mutation in ClC-7 causing autosomal dominant osteopetrosis type II (Q24672242)

2

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Sophie Schaller

3

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Bjarne H Dahl

4

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Morten H Dziegiel

5

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Jens Bollerslev

6

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Morten A Karsdal

The American Journal of Pathology

7

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language of work or name

English

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publication date

May 2004

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published in

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volume

164

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issue

5

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page(s)

1537-45

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cites work

X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity

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Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II

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Chloride channel 7 (CLCN7) gene mutations in intermediate autosomal recessive osteopetrosis

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Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

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

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The a3 Isoform of the 100-kDa V-ATPase Subunit Is Highly but Differentially Expressed in Large (≥10 Nuclei) and Small (≤5 Nuclei) Osteoclasts

7 April 2017

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Matrix metalloproteinases (MMP) and cathepsin K contribute differently to osteoclastic activities

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Genotype-phenotype relationship in human ATP6i-dependent autosomal recessive osteopetrosis

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Molecular structure and physiological function of chloride channels

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Establishment and characterization of tartrate-resistant acid phosphatase and alkaline phosphatase double positive cell lines

28 September 2017

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Resorptive state and cell size influence intracellular pH regulation in rabbit osteoclasts cultured on collagen-hydroxyapatite films

28 September 2017

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A selective inhibitor of the osteoclastic V-H(+)-ATPase prevents bone loss in both thyroparathyroidectomized and ovariectomized rats

28 September 2017

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Osteoclast molecular phenotyping by random cDNA sequencing

28 September 2017

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Autosomal dominant osteopetrosis: bone mineral measurements of the entire skeleton of adults in two different subtypes.

28 September 2017

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Chloride channels of intracellular organelles.

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Cell-mediated extracellular acidification and bone resorption: evidence for a low pH in resorbing lacunae and localization of a 100-kD lysosomal membrane protein at the osteoclast ruffled border

28 September 2017

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Heterogeneity of autosomal dominant osteopetrosis

28 September 2017

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Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis

28 September 2017

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Autosomal dominant osteopetrosis: bone metabolism and epidemiological, clinical, and hormonal aspects

28 September 2017

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Osteoclastic bone resorption by a polarized vacuolar proton pump

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Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders

28 September 2017

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Ultrastructural investigations of bone resorptive cells in two types of autosomal dominant osteopetrosis.

30 May 2018

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Autosomal dominant osteopetrosis: an otoneurological investigation of the two radiological types

30 May 2018

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Biochemical evidence of disturbed bone metabolism and calcium homeostasis in two types of autosomal dominant osteopetrosis.

30 May 2018

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Inhibition of osteoclast proton transport by bafilomycin A1 abolishes bone resorption

30 May 2018

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The chloride channel inhibitor NS3736 [corrected] prevents bone resorption in ovariectomized rats without changing bone formation.

30 May 2018

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A potent small molecule, nonpeptide inhibitor of cathepsin K (SB 331750) prevents bone matrix resorption in the ovariectomized rat.

28 November 2018

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Measurement of tartrate-resistant acid phosphatase and the brain isoenzyme of creatine kinase accurately diagnoses type II autosomal dominant osteopetrosis but does not identify gene carriers

28 November 2018

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28 November 2018

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

28 November 2018

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

28 November 2018

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Cathepsin K Knockout Mice Develop Osteopetrosis Due to a Deficit in Matrix Degradation but Not Demineralization

28 November 2018

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Cortical bone remodeling in autosomal dominant osteopetrosis: a study of two different phenotypes.

28 November 2018

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Structural and histomorphometric studies of iliac crest trabecular and cortical bone in autosomal dominant osteopetrosis: a study of two radiological types

28 November 2018

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Elevated serum levels of creatine kinase BB in autosomal dominant osteopetrosis type II

7 January 2021

1 reference

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Higher osteoclastic demineralization and highly mineralized cement lines with osteocalcin deposition in a mandibular cortical bone of autosomal dominant osteopetrosis type II: ultrastructural and undecalcified histological investigations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963712-1

Transforming growth factor-beta controls human osteoclastogenesis through the p38 MAPK and regulation of RANK expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963712-1

Peptide aldehyde inhibitors of cathepsin K inhibit bone resorption both in vitro and in vivo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2963712-1

Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier

7 January 2021

1 reference

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Functional heterogeneity of osteoclasts: matrix metalloproteinases participate in osteoclastic resorption of calvarial bone but not in resorption of long bone

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15111300

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)63712-1

1 reference

3986749

3986749

1 reference

1 reference

1 reference