Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man (Q28201425)

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D Kasper

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M R Bösl

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E Kaiser

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M Schweizer

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A Schulz

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W Friedrich

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G Delling

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T J Jentsch

Chloride channels of intracellular organelles.

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language of work or name

English

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publication date

26 January 2001

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published in

Cell

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volume

104

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issue

2

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page(s)

205-15

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Axotomy results in delayed death and apoptosis of retinal ganglion cells in adult rats.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Osteoclastic bone resorption by a polarized vacuolar proton pump

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Biochemical markers of bone metabolism: an overview

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

The yeast CLC chloride channel functions in cation homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

The GEF1 gene of Saccharomyces cerevisiae encodes an integral membrane protein; mutations in which have effects on respiration and iron-limited growth

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

The CLC chloride channel family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Retinal atrophy in osteopetrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Osteopetrosis and osteoporosis: two sides of the same coin

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Trafficking of Matrix Collagens Through Bone-Resorbing Osteoclasts

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Molecular cloning and expression of three isoforms of the 100-kDa a subunit of the mouse vacuolar proton-translocating ATPase.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Removal of osteoclast bone resorption products by transcytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

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://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Inactivation of muscle chloride channel by transposon insertion in myotonic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Disruption of ClC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

Three subunit a isoforms of mouse vacuolar H(+)-ATPase. Preferential expression of the a3 isoform during osteoclast differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021

The bone marrow-derived stromal cell lines MC3T3-G2/PA6 and ST2 support osteoclast-like cell differentiation in cocultures with mouse spleen cells

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2801%2900206-9

7 January 2021