Family of Na+, K+‐ATPase genes Intra‐individual tissue‐specific restriction fragment length polymorphism

  title={Family of Na+, K+‐ATPase genes Intra‐individual tissue‐specific restriction fragment length polymorphism},
  author={Eugene D. Sverdlov and Natalia E. Broude and Vladimir E. Sverdlov and Galina Sergeevna Monastyrskaya and Alexander V Grishin and K. E. Petrukhin and N. S. Akopyanz and Nikolai N. Modyanov and Yu. A. Ovchinnikov},
  journal={FEBS Letters},
9 Citations
A plasma membrane‐type Ca2+‐ATPase co‐localizes with a vacuolar H+‐pyrophosphatase to acidocalcisomes of Toxoplasma gondii
Cloning and sequencing of a gene encoding a plasma membrane‐type Ca2+‐ATPase of T.gondii indicate that TgA1 localizes to the plasma membrane and co‐localizes with the vacuolar H+‐pyrophosphatase to intracellular vacuoles identified morphologically and by X‐ray microanalysis as the acidocalcisomes.
Na+, K(+)-ATPase isoforms in the retina.
Trypanosoma brucei Plasma Membrane-Type Ca2+-ATPase 1 (TbPMC1) and 2 (TbPMC2) Genes Encode Functional Ca2+-ATPases Localized to the Acidocalcisomes and Plasma Membrane, and Essential for Ca2+ Homeostasis and Growth*
The cloning and sequencing of two genes encoding plasma membrane-type Ca2+-ATPases (PMCAs) of T. brucei are reported to establish that they are essential for parasite viability and validate them as targets for drug development.
Functional genomic assessment of phosgene-induced acute lung injury in mice.
A gene with a suggestive SNP association, Itga9, is linked to transforming growth factor β1 signaling, which previously has been associated with the susceptibility to ALI in mice.
Isozymes of the Na+/K+-ATPase.
  • K. Sweadner
  • Chemistry, Medicine
    Biochimica et biophysica acta
  • 1989


Primary structure of the α-subunit of Torpedo californica (Na+ + K+)ATPase deduced from cDNA sequence
Cloned and sequenced DNA complementary to the Torpedo californica electroplax messenger RNA encoding the α-subunit of (Na+ + K+)ATPase is cloned and deduced the complete ammo-acid sequence of the polypeptide.
Molecular cloning of three distinct forms of the Na+,K+-ATPase alpha-subunit from rat brain.
A lysine-rich sequence that may function as a movable, ion-selective gate during cation binding and occlusion and several amino acid sequence variations that appear to explain some of the well-known species and tissue differences in cardiac glycoside sensitivity are identified.
Structure of the human immune interferon gene
All the evidence to date and the present data suggest that this is the only gene for IFN-γ and that the resolution of IFn-γ into two components18 is probably the result of post-translational processing of the protein.
Amino-acid sequence of the catalytic subunit of the (Na+ + K+)ATPase deduced from a complementary DNA
A complementary DNA for the catalytic subunit of the sheep kidney sodium / potassium-dependent ATPase is isolated and characterized and is linked to the phosphorylation site by a 60-amino-acid conserved sequence that may be a major channel for energy transduction.
Genomic sequencing.
  • G. Church, W. Gilbert
  • Biology, Chemistry
    Proceedings of the National Academy of Sciences of the United States of America
  • 1984
The genomic sequencing procedures are applicable to the analysis of genetic polymorphisms, DNA methylation at deoxycytidines, and nucleic acid-protein interactions at single nucleotide resolution.
Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose.
  • H. Aviv, P. Leder
  • Biology, Chemistry
    Proceedings of the National Academy of Sciences of the United States of America
  • 1972
A convenient technique for the partial purification of large quantities of functional, poly(adenylic acid)-rich mRNA is described and should prove generally useful as an initial step in the isolation of specific mRNAs.
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.
  • P. Thomas
  • Biology, Chemistry
    Proceedings of the National Academy of Sciences of the United States of America
  • 1980
A simple and rapid method for transferring RNA from agarose gels to nitrocellulose paper for blot hybridization has been developed, allowing removal of the hybridized probes and rehybridization of the RNA blots without loss of sensitivity.