Results 141 to 150 of about 3,909 (203)
Assessing the Functional Significance of Novel and Rare Variants of the <i>SLC26A4</i> Gene Found in Patients with Hearing Loss by Minigene Assay. [PDF]
Int J Mol SciDanilchenko VY +4 more
europepmc +1 more source
Prevalence of pendrin defects in sudanese families with congenital hypothyroidism. [PDF]
EndocrineIslam MS +4 more
europepmc +1 more source
The K-Cl cotransporter-3 in the mammalian kidney. [PDF]
Curr Opin Nephrol Hypertens, 2023 Ferdaus MZ, Delpire E.
europepmc +1 more source
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct. [PDF]
Mol MedBernardinelli E +7 more
europepmc +1 more source
Cystic fibrosis-related kidney disease-emerging morbidity and disease modifier. [PDF]
Pediatr NephrolHart M +5 more
europepmc +1 more source
Structural basis for substrate recognition mechanism of human SLC26A7. [PDF]
Nat CommunLi X +10 more
europepmc +1 more source
Hypokalemia and Pendrin Induction by Aldosterone
Hypokalemia and Pendrin Induction by AldosteroneAldosterone plays an important role in regulating Na-Cl reabsorption and blood pressure. Epithelial Na+ channel, Na+-Cl- cotransporter, and Cl-/HCO3- exchanger pendrin are the major mediators of Na-Cl transport in the aldosterone-sensitive distal nephron. Existing evidence also suggests that plasma K+ concentration affects renal Na-Cl handling. In this
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Nitric oxide reduces renal pendrin abundance
The FASEB Journal, 2011 Monika Thumova +3 more
openaire +1 more source