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Here we show mice homozygous for R740S (R740S/R740S) of the Vacuolar-type H(+)-ATPases have more severe osteopetrosis (show CSF1 ELISA Kits) and die by postnatal day 14
Luteolin can be effective in reducing bone resorption and that this effect of luteolin may be through disruption of osteoclast V-ATPase a3-d2 interaction.
increased lysosomal pH in V ATPase a3 mutant mice osteoclasts leads to decreased NFATc1 (show NFATC1 ELISA Kits) signaling and nuclear translocation, resulting in a cell autonomous impairment of osteoclastogenesis in vitro.
These results demonstrate that adeno (show ADORA2A ELISA Kits)-associated virus-mediated Atp6i/TIRC7 knockdown in periapical tissues can inhibit endodontic disease development, bone resorption, and inflammation.
The N termini of a-subunit isoforms are involved in signaling between vacuolar H+-ATPase (show ATP6V1B2 ELISA Kits) (V-ATPase (show DNAH8 ELISA Kits)) and cytohesin-2 (show CYTH2 ELISA Kits)
we report for the first time on biological effects mediated by a peptide corresponding to the C-terminus of Tirc7 protein, which interfere with monocytic differentiation pathways.
Tcirg1, which is essential for osteoclasts to pump protons into the bone, is not appreciably expressed in maturation stage mouse ameloblasts.
ocular phenotype of mice deficient in Tcirg1 function
V-ATPase (show ATP6V1H ELISA Kits) localization and activity in kidney cells via direct PKA-dependent phosphorylation of the A subunit at Ser-175
RANKL (show TNFSF11 ELISA Kits) treatment releases the negative regulation of PARP-1 (show PARP1 ELISA Kits) on Tcirg1 gene expression during osteoclastogenesis
TCIRG1 may be involved in endolysosomal transport-a process known to be important to development of early onset AD.
TCIRG1 gene mutation in a Chinese family is associated with infantile malignant osteopetrosis (show CSF1 ELISA Kits).
Nine rare missense variants at evolutionarily conserved sites in TCIRG1 are associated with lower absolute neutrophil count.
an intronic region in TCIRG1 that seems to be particularly prone to splicing mutations, allowing the production of a small amount of protein sufficient to reduce the severity of the phenotype usually associated with TCIRG1 defects.
TIRC7 might be involved in the pathogenesis of aplastic anemia.
An A to T transversion in the fourth base of the intron 2 donor splice site (c.117+4A-->T) in TCIRG1 in the Ashkenazi Jewish (AJ) population was found to be responsible for osteopetrosis (show CSF1 ELISA Kits).
TIRC7 might be associated with the pathogenesis of ITP (show ITPA ELISA Kits), and TIRC7 levels could be used as an indicator to evaluate patients' response to HD-DXM treatment.
Increased expression of TIRC7 in plasma was associated with the severity of acute graft-versus-host disease.
Data indicate that the effects of epiregulin (EREG (show EREG ELISA Kits)) and V-ATPase (show ATP6V1H ELISA Kits) (TCIRG1) single nucleotide polymorphism (SNP) on pulmonary tuberculosis susceptibility, to the extent that they exist, are dependent on gene-gene interactions in West African populations.
TCIRG1-associated congenital neutropenia.
Through alternate splicing, this gene encodes two proteins with similarity to subunits of the vacuolar ATPase (V-ATPase) but the encoded proteins seem to have different functions. V-ATPase is a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, and receptor-mediated endocytosis. V-ATPase is comprised of a cytosolic V1 domain and a transmembrane V0 domain. Mutations in this gene are associated with infantile malignant osteopetrosis.
ATPase, H+ transporting, lysosomal V0 protein a
, T cell immune response cDNA7 protein
, T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3
, T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein a
, V-type proton ATPase 116 kDa subunit a
, V-type proton ATPase 116 kDa subunit a isoform 3
, osteoclastic proton pump
, v-ATPase 116-kDa
, v-H+ATPase subunit a3
, ATPase, H+ transporting, lysosomal I
, T-cell, immune regulator 1
, V-ATPase a3
, ATPase, H+ transporting, 116kD
, OC-116 kDa
, T-cell immune response cDNA 7
, V-ATPase 116-kDa
, osteoclastic proton pump 116 kDa subunit
, specific 116-kDa vacuolar proton pump subunit
, vacuolar proton translocating ATPase 116 kDa subunit A