(Q24299288)

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Vacuolar H+-ATPase d2 subunit: molecular characterization, developmental regulation, and localization to specialized proton pumps in kidney and bone

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scholarly article

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Vacuolar H+-ATPase d2 subunit: molecular characterization, developmental regulation, and localization to specialized proton pumps in kidney and bone (English)

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ATPase H+ transporting V0 subunit a4

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GOA release 2020-03-11

T cell immune regulator 1, ATPase H+ transporting V0 subunit a3

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GOA release 2020-03-11

ATPase H+ transporting V0 subunit d2

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GOA release 2020-03-11

Olivier Devuyst

12

object named as

Olivier Devuyst

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object named as

Fiona E Karet

13

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object named as

Anna Villa

10

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Valérie Cormier-Daire

object named as

Valerie Cormier-Daire

8

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François Jouret

2

object named as

François Jouret

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author name string

Annabel N Smith

1

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Sharyn Bord

3

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Katherine J Borthwick

4

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Rafia S Al-Lamki

5

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Carsten A Wagner

6

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Deborah C Ireland

7

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Annalisa Frattini

9

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Uwe Kornak

11

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language of work or name

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publication date

May 2005

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Journal of the American Society of Nephrology

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16

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5

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1245-56

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Identification of a novel mutation in the coding region of the grey-lethal gene OSTM1 in human malignant infantile osteopetrosis

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Molecular cloning and characterization of a putative novel human osteoclast-specific 116-kDa vacuolar proton pump subunit

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Postnatal development of H+ ATPase (proton-pump)-rich cells in rat epididymis.

1 reference

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Postnatal expression of transport proteins involved in acid-base transport in mouse kidney

1 reference

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based on heuristic

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The putative 116 kDa osteoclast specific vacuolar proton pump subunit has ubiquitous tissue distribution

1 reference

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based on heuristic

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A human gene, ATP6E1, encoding a testis-specific isoform of H(+)-ATPase subunit E

1 reference

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Molecular cloning and characterization of novel tissue-specific isoforms of the human vacuolar H(+)-ATPase C, G and d subunits, and their evaluation in autosomal recessive distal renal tubular acidosis

1 reference

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Diversity of mouse proton-translocating ATPase: presence of multiple isoforms of the C, d and G subunits

1 reference

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Molecular cloning and characterization of Atp6v1b1, the murine vacuolar H+-ATPase B1-subunit

1 reference

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

1 reference

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

1 reference

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

1 reference

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based on heuristic

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

1 reference

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The vacuolar (H+)-ATPases--nature's most versatile proton pumps

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A novel inhibitor of vacuolar ATPase, FR167356, which can discriminate between osteoclast vacuolar ATPase and lysosomal vacuolar ATPase

1 reference

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based on heuristic

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Heterogeneity of vacuolar H(+)-ATPase: differential expression of two human subunit B isoforms

1 reference

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based on heuristic

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Crystal structure of a central stalk subunit C and reversible association/dissociation of vacuole-type ATPase

1 reference

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Polymorphic DNA region adjacent to the 5' end of the human insulin gene

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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

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Selectively amplified expression of an isoform of the vacuolar H(+)-ATPase 56-kilodalton subunit in renal intercalated cells

1 reference

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7 January 2021

based on heuristic

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Vacuolar H+-ATPase in ocular ciliary epithelium

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based on heuristic

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

1 reference

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based on heuristic

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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/10.1681%2FASN.2004090761

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based on heuristic

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

1 reference

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7 January 2021

based on heuristic

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a4, a unique kidney-specific isoform of mouse vacuolar H+-ATPase subunit a

1 reference

https://api.crossref.org/works/10.1681%2FASN.2004090761

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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From lysosomes to the plasma membrane: localization of vacuolar-type H+ -ATPase with the a3 isoform during osteoclast differentiation

1 reference

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7 January 2021

based on heuristic

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Expression and function of the mouse V-ATPase d subunit isoforms

1 reference

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based on heuristic

inferred from DOI database lookup

Mouse proton pump ATPase C subunit isoforms (C2-a and C2-b) specifically expressed in kidney and lung.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

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The yeast vacuolar proton-translocating ATPase contains a subunit homologous to the Manduca sexta and bovine e subunits that is essential for function

1 reference

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Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease

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

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Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis

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Comparative ontogeny, processing, and segmental distribution of the renal chloride channel, ClC-5

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Osteoclastic bone resorption by a polarized vacuolar proton pump

1 reference

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Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

1 reference

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Physiology and biochemistry of the kidney vacuolar H+-ATPase

1 reference

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Characterization of mouse Atp6i gene, the gene promoter, and the gene expression.

1 reference

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

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Identifiers

10.1681/ASN.2004090761

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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