Skip to search formSkip to main contentSkip to account menu
Amiloride: a molecular probe of sodium transport in tissues and cells.
  • D. Benos
  • Biology
    The American journal of physiology
  • 1 March 1982
TLDR
This drug is the most potent and specific inhibitor of Na+ entry found to date and thus affords the opportunity to be used as a label for the isolation of these transport moieties.
View on PubMed
NaCl uptake by the branchial epithelium in freshwater teleost fish: an immunological approach to ion-transport protein localization.
TLDR
A freshwater-type MR chloride cell exists in teleost fishes, and the NHE-like immunoreactivity is associated with the accessory cell type and with a small population of pavement cells in tilapia and rainbow trout.
View on PubMed
Guidelines for reporting statistics in journals published by the American Physiological Society.
TLDR
Based on the incidence of standard deviations, standard errors, and confidence intervals in articles published by the American Physiological Society, many scientists appear to misunderstand fundamental concepts and procedures in statistics.
View on PubMed
The ups and downs of peer review.
TLDR
The merits of peer review and its weaknesses, both perceived and real, as well as the practicalities of several major proposed changes to the system are discussed.
View on PubMed
Guidelines for reporting statistics in journals published by the American Physiological Society.
TLDR
Based on the incidence of standard deviations, standard errors, and confidence intervals in articles published by the American Physiological Society, many scientists appear to misunderstand fundamental concepts and procedures in statistics.
View on PubMed
CFTR is a conductance regulator as well as a chloride channel.
TLDR
This review focuses on a plethora of studies showing that CFTR also regulates other ion channel proteins, and it is the hope of the authors that the reader will take with him or her the message thatCFTR is a conductance regulator as well as a Cl- channel.
View on PubMed
Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms
TLDR
It is shown that cystic fibrosis gene encodes a cyclic AMP-gated chloride channel that mediates electrolyte transport across the luminal surfaces of a variety of epithelial cells and is regulated by an epithelially expressed syntaxin (syntaxin 1A), a membrane protein that also modulates neurosecretion and calcium-channel gating in brain.
View on Springer
Cloning of an Epithelial Chloride Channel from Bovine Trachea (*)
TLDR
It is suggested that either the 140-kDa translated product is a prepro form of the 38-k Da subunit of the previously identified bovine tracheal anion channel and that the primary transcript is post-translationally cleaved to yield the final product, or that the cloned channel and the previously identify bovines trachea anionChannel protein share an epitope that is recognized by the αp38 antibody.
View on Publisher
Mammalian blastocyst: transport functions in a developing epithelium.
TLDR
The current state of knowledge concerning morphological and physiological mechanisms important to growth and differentiation of the mammalian blastocyst between compaction and implantation are reviewed.
View on PubMed
Cystic Fibrosis Transmembrane Conductance Regulator Facilitates ATP Release by Stimulating a Separate ATP Release Channel for Autocrine Control of Cell Volume Regulation*
TLDR
These studies provide evidence that cystic fibrosis transmembrane conductance regulator potentiates and accelerates regulatory volume decrease (RVD) following hypotonic challenge by an autocrine mechanism involving ATP release and signaling and suggest that CFTR potentiates ATP release by stimulating a separate ATP channel to strengthen autocrine control of cell volume regulation.
View on Publisher
...
...
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License