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

@article{Sverdlov1987FamilyON,
  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},
  year={1987},
  volume={221}
}
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9 Citations

9 Citations

Citation Type

Citation Type

Na+, K+‐ATPase: Tissue‐specific expression of genes coding for α‐subunit in diverse human tissues
Advances in Na+,K+‐ATPase studies: from protein to gene and back to protein
Family of human Na+,K+‐ATPase genes Structure of the putative regulatory region of the α+‐gene
Family of human Na+,K+‐ATPase genes Structure of the gene for the catalytic subunit (αIII‐form) and its relationship with structural features of the protein
A plasma membrane‐type Ca2+‐ATPase co‐localizes with a vacuolar H+‐pyrophosphatase to acidocalcisomes of Toxoplasma gondii
TLDR
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*
TLDR
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.
TLDR
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

References

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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.
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