Matches in SemOpenAlex for { <https://semopenalex.org/work/W2148494499> ?p ?o ?g. }
- W2148494499 endingPage "59" @default.
- W2148494499 startingPage "51" @default.
- W2148494499 abstract "Renal tubular acidosis (RTA) is characterized by metabolic acidosis due to renal impaired acid excretion. Hyperchloremic acidosis with normal anion gap and normal or minimally affected glomerular filtration rate defines this disorder. RTA can also present with hypokalemia, medullary nephrocalcinosis and nephrolitiasis, as well as growth retardation and rickets in children, or short stature and osteomalacia in adults. In the past decade, remarkable progress has been made in our understanding of the molecular pathogenesis of RTA and the fundamental molecular physiology of renal tubular transport processes. This review summarizes hereditary diseases caused by mutations in genes encoding transporter or channel proteins operating along the renal tubule. Review of the molecular basis of hereditary tubulopathies reveals various loss-of-function or gain-of-function mutations in genes encoding cotransporter, exchanger, or channel proteins, which are located in the luminal, basolateral, or endosomal membranes of the tubular cell or in paracellular tight junctions. These gene mutations result in a variety of functional defects in transporter/channel proteins, including decreased activity, impaired gating, defective trafficking, impaired endocytosis and degradation, or defective assembly of channel subunits. Further molecular studies of inherited tubular transport disorders may shed more light on the molecular pathophysiology of these diseases and may significantly improve our understanding of the mechanisms underlying renal salt homeostasis, urinary mineral excretion, and blood pressure regulation in health and disease. The identification of the molecular defects in inherited tubulopathies may provide a basis for future design of targeted therapeutic interventions and, possibly, strategies for gene therapy of these complex disorders. Keywords: Renal tubular acidosis, acid-base homeostasis, molecular physiology, tubular transport, gene mutations" @default.
- W2148494499 created "2016-06-24" @default.
- W2148494499 creator A5064839258 @default.
- W2148494499 creator A5076820886 @default.
- W2148494499 creator A5076979842 @default.
- W2148494499 creator A5088732408 @default.
- W2148494499 date "2009-03-01" @default.
- W2148494499 modified "2023-09-25" @default.
- W2148494499 title "Molecular Pathophysiology of Renal Tubular Acidosis" @default.
- W2148494499 cites W129717176 @default.
- W2148494499 cites W1533109364 @default.
- W2148494499 cites W1947834585 @default.
- W2148494499 cites W1975970390 @default.
- W2148494499 cites W1983638877 @default.
- W2148494499 cites W1985455923 @default.
- W2148494499 cites W1990587990 @default.
- W2148494499 cites W1993697399 @default.
- W2148494499 cites W1995620131 @default.
- W2148494499 cites W1995773817 @default.
- W2148494499 cites W1996499484 @default.
- W2148494499 cites W2000396915 @default.
- W2148494499 cites W2004953882 @default.
- W2148494499 cites W2009050455 @default.
- W2148494499 cites W2010418177 @default.
- W2148494499 cites W2019688274 @default.
- W2148494499 cites W2029209604 @default.
- W2148494499 cites W2030589408 @default.
- W2148494499 cites W2056490931 @default.
- W2148494499 cites W2061221721 @default.
- W2148494499 cites W2067541932 @default.
- W2148494499 cites W2072903395 @default.
- W2148494499 cites W2073876005 @default.
- W2148494499 cites W2080987000 @default.
- W2148494499 cites W2082719247 @default.
- W2148494499 cites W2086915337 @default.
- W2148494499 cites W2087050036 @default.
- W2148494499 cites W2088380869 @default.
- W2148494499 cites W2097456656 @default.
- W2148494499 cites W2103083708 @default.
- W2148494499 cites W2106666091 @default.
- W2148494499 cites W2109554821 @default.
- W2148494499 cites W2112150224 @default.
- W2148494499 cites W2118527116 @default.
- W2148494499 cites W2118613002 @default.
- W2148494499 cites W2118792580 @default.
- W2148494499 cites W2121193330 @default.
- W2148494499 cites W2124678488 @default.
- W2148494499 cites W2131398176 @default.
- W2148494499 cites W2140592163 @default.
- W2148494499 cites W2142766228 @default.
- W2148494499 cites W2150463659 @default.
- W2148494499 cites W2157194582 @default.
- W2148494499 cites W2160018480 @default.
- W2148494499 cites W2160953172 @default.
- W2148494499 cites W2162415185 @default.
- W2148494499 cites W2164820318 @default.
- W2148494499 cites W2167235167 @default.
- W2148494499 cites W2175268283 @default.
- W2148494499 cites W2176888636 @default.
- W2148494499 cites W2186994815 @default.
- W2148494499 cites W2324300516 @default.
- W2148494499 cites W2329235470 @default.
- W2148494499 cites W2419039010 @default.
- W2148494499 cites W137527499 @default.
- W2148494499 cites W3139843180 @default.
- W2148494499 doi "https://doi.org/10.2174/138920209787581262" @default.
- W2148494499 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2699831" @default.
- W2148494499 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19721811" @default.
- W2148494499 hasPublicationYear "2009" @default.
- W2148494499 type Work @default.
- W2148494499 sameAs 2148494499 @default.
- W2148494499 citedByCount "65" @default.
- W2148494499 countsByYear W21484944992012 @default.
- W2148494499 countsByYear W21484944992013 @default.
- W2148494499 countsByYear W21484944992014 @default.
- W2148494499 countsByYear W21484944992015 @default.
- W2148494499 countsByYear W21484944992016 @default.
- W2148494499 countsByYear W21484944992017 @default.
- W2148494499 countsByYear W21484944992018 @default.
- W2148494499 countsByYear W21484944992019 @default.
- W2148494499 countsByYear W21484944992020 @default.
- W2148494499 countsByYear W21484944992021 @default.
- W2148494499 countsByYear W21484944992022 @default.
- W2148494499 countsByYear W21484944992023 @default.
- W2148494499 crossrefType "journal-article" @default.
- W2148494499 hasAuthorship W2148494499A5064839258 @default.
- W2148494499 hasAuthorship W2148494499A5076820886 @default.
- W2148494499 hasAuthorship W2148494499A5076979842 @default.
- W2148494499 hasAuthorship W2148494499A5088732408 @default.
- W2148494499 hasBestOaLocation W21484944992 @default.
- W2148494499 hasConcept C126322002 @default.
- W2148494499 hasConcept C134018914 @default.
- W2148494499 hasConcept C2776356786 @default.
- W2148494499 hasConcept C2776777027 @default.
- W2148494499 hasConcept C2778553927 @default.
- W2148494499 hasConcept C2778573388 @default.
- W2148494499 hasConcept C2779026464 @default.
- W2148494499 hasConcept C2780091579 @default.