(Q44961480)

7 December 2017

title

In vitro differentiation of CD14 cells from osteopetrotic subjects: contrasting phenotypes with TCIRG1, CLCN7, and attachment defects (English)

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7 December 2017

3

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7 December 2017

Harry C Blair

1

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7 December 2017

Christopher W Borysenko

2

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7 December 2017

Paul H Schlesinger

4

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7 December 2017

Sara E Kalla

5

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7 December 2017

Beatrice B Yaroslavskiy

6

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7 December 2017

Verónica Garćia-Palacios

7

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7 December 2017

Jennifer I Oakley

8

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7 December 2017

Paul J Orchard

9

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7 December 2017

publication date

5 April 2004

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Journal of Bone and Mineral Research

7 December 2017

published in

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7 December 2017

volume

19

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7 December 2017

issue

8

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7 December 2017

page(s)

1329-1338

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Mechanisms balancing skeletal matrix synthesis and degradation

7 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Osteopetrosis in mice lacking haematopoietic transcription factor PU.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Congenital osteoclast deficiency in osteopetrotic (op/op) mice is cured by injections of macrophage colony-stimulating factor

21 January 2018

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https://api.crossref.org/works/10.1359%2FJBMR.040403

Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency

21 January 2018

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https://api.crossref.org/works/10.1359%2FJBMR.040403

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Novel mutations in the a3 subunit of vacuolar H(+)-adenosine triphosphatase in a Japanese patient with infantile malignant osteopetrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Complete genomic structure of the CLCN6 and CLCN7 putative chloride channel genes(1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structures.

21 January 2018

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https://api.crossref.org/works/10.1359%2FJBMR.040403

Autocrine and paracrine nitric oxide regulate attachment of human osteoclasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Proteolytic activity of human osteoclast cathepsin K. Expression, purification, activation, and substrate identification

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Proteinase expression during differentiation of human osteoclasts in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

The mutational spectrum of human malignant autosomal recessive osteopetrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

The ClC-5 knockout mouse model of Dent's disease has renal hypercalciuria and increased bone turnover

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Proteolysis of latent transforming growth factor-beta (TGF-beta )-binding protein-1 by osteoclasts. A cellular mechanism for release of TGF-beta from bone matrix.

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Rescue of osteoclast function by transgenic expression of kinase-deficient Src in src-/- mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Extracellular protons acidify osteoclasts, reduce cytosolic calcium, and promote expression of cell-matrix attachment structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

c-Fms and the alphavbeta3 integrin collaborate during osteoclast differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Characterization of the Osteoclast Ruffled Border Chloride Channel and Its Role in Bone Resorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Colony Stimulating Factor-1-Induced Osteoclast Spreading Depends on Substrate and Requires the Vitronectin Receptor and the c-src Proto-Oncogene

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

Upregulation of osteoclast alpha2beta1 integrin compensates for lack of alphavbeta3 vitronectin receptor in Iraqi-Jewish-type Glanzmann thrombasthenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1359%2FJBMR.040403

21 January 2018

Identifiers

DOI

10.1359/JBMR.040403

1 reference

7 December 2017

1 reference