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ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2

ATP6V0D2
Top mentioned proteins: ATPase, A-4, ATP6V1G3, ACID, V-ATPase
Papers on ATP6V0D2
Identification of novel osteochondrosis- associated genes.
New
Mackie et al., Melbourne, Australia. In J Orthop Res, Sep 2015
Genes encoding vacuolar H(+) -ATPase V0 subunit d2 (ATP6V0D2), cathepsin K, integrin-binding sialoprotein, integrin αV, low density lipoprotein receptor-related protein 4, lumican, osteopontin, and thymosin β4 (TMSB4) were expressed at higher levels in lesions than in control cartilage.
Expression of acidosis-dependent genes in human cancer nests.
Kobayashi et al., Chiba, Japan. In Mol Clin Oncol, 2014
Therefore, 7 genes were selected from our previous study, which encoded interleukin 32 (IL-32), lysosomal H(+) transporting ATPase, V0 subunit d2 (ATP6V0D2), tumor necrosis factor receptor superfamily, member 9 (TNFRSF9), amphiregulin, schwannoma-derived growth factor (AREG), v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (ErbB3), PRR5-ARHGAP8 (LOC553158) and dimethylglycine dehydrogenase (DMGDH), and their expression was examined in human clinical specimens from patients with cancer.
Establishing an osteosarcoma associated protein-protein interaction network to explore the pathogenesis of osteosarcoma.
Cai et al., Shanghai, China. In Eur J Med Res, 2012
Genes such as HRAS, IDH3A, ATP6ap1, ATP6V0D2, SEMA3F and SEMA3A were involved in the enriched pathways.
Adrm1 interacts with Atp6v0d2 and regulates osteoclast differentiation.
GeneRIF
Choi et al., Philadelphia, United States. In Biochem Biophys Res Commun, 2010
these data suggest that Adrm1, a new Atp6v0d2-interacting protein, plays an important role in osteoclast differentiation, and in particular the fusion of preosteoclasts.
The proton pump inhibitor inhibits cell growth and induces apoptosis in human hepatoblastoma.
Satomi et al., Saitama, Japan. In Pediatr Surg Int, 2008
Moreover, the analysis of hepatoblastoma cells using the gene Chip gene expression analysis arrays showed that three of the 27 V-ATPase-related transcripts (ATP6V0D2, ATP6V1B1, and ATP6V0A1) were more weakly expressed in the Baf-A1-treated cells than in the Baf-A1-free cells.
Distinct expression patterns of different subunit isoforms of the V-ATPase in the rat epididymis.
Breton et al., Boston, United States. In Biol Reprod, 2006
Here, we report the localization of V-ATPase subunit isoforms ATP6V1A, ATP6V1C1, ATP6V1C2, ATP6V1G1, ATP6V1G3, ATP6V0A1, ATP6V0A2, ATP6V0A4, ATP6V0D1, and ATP6V0D2, previously labeled A, C1, C2, G1, G3, a1, a2, a4, d1, and d2, in epithelial cells of the rat epididymis and vas deferens.
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.
Karet et al., Cambridge, United Kingdom. In Gene, 2002
Here we report the cloning of three previously uncharacterized human genes, ATP6V1C2, ATP6V1G3 and ATP6V0D2, encoding novel H(+)-ATPase subunit isoforms C2, G3 and d2, respectively.
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