Pages that link to "Q33942447"
Jump to navigation
Jump to search
The following pages link to Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney (Q33942447):
Displaying 20 items.
- NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation (Q24311258) (← links)
- Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11 (Q24647552) (← links)
- SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy (Q26785510) (← links)
- Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature (Q27003290) (← links)
- Transport and regulatory characteristics of the yeast bicarbonate transporter homolog Bor1p (Q27932256) (← links)
- The SLC4 family of HCO 3 - transporters (Q28238660) (← links)
- The forkhead transcription factor Foxi1 directly activates the AE4 promoter (Q28513920) (← links)
- AE4 is a DIDS-sensitive Cl(-)/HCO(-)(3) exchanger in the basolateral membrane of the renal CCD and the SMG duct (Q28575883) (← links)
- SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria. (Q28590585) (← links)
- Expression and localization of Na-driven Cl-HCO(3)(-) exchanger (SLC4A8) in rodent CNS (Q28594378) (← links)
- The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transporters (Q30440948) (← links)
- Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities (Q30479480) (← links)
- Transport of H2S and HS(-) across the human red blood cell membrane: rapid H2S diffusion and AE1-mediated Cl(-)/HS(-) exchange (Q33702662) (← links)
- Glutaminolysis is Essential for Energy Production and Ion Transport in Human Corneal Endothelium. (Q33809428) (← links)
- The SLC4 family of bicarbonate (HCO₃⁻) transporters (Q34333694) (← links)
- Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). (Q34536951) (← links)
- Fuchs Endothelial Corneal Dystrophy (Q34624570) (← links)
- Structural determinants and significance of regulation of electrogenic Na(+)-HCO(3)(-) cotransporter stoichiometry (Q34953449) (← links)
- Human SLC4A11-C functions as a DIDS-stimulatable H⁺(OH⁻) permeation pathway: partial correction of R109H mutant transport (Q34980472) (← links)
- Bicarbonate transport proteins. (Q35003109) (← links)