Pages that link to "Q38748793"
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The following pages link to Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants (Q38748793):
Displaying 14 items.
- SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations (Q30396131) (← links)
- Comprehensive characterization of DNA methylation changes in Fuchs endothelial corneal dystrophy (Q36338076) (← links)
- Conditionally Immortal Slc4a11-/- Mouse Corneal Endothelial Cell Line Recapitulates Disrupted Glutaminolysis Seen in Slc4a11-/- Mouse Model. (Q38696524) (← links)
- Vps35-deficiency impairs SLC4A11 trafficking and promotes corneal dystrophy (Q41866630) (← links)
- H(OH), H(OH), H(OH): a holiday perspective. Focus on "Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH- conductance pathway that is stimulated by rises in intracellular and extracellular pH". (Q46370115) (← links)
- Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies (Q47719851) (← links)
- Expression of SLC4A11 protein in mouse and rat medulla: a candidate transporter involved in outer medullary ammonia recycling (Q64280967) (← links)
- R125H, W240S, C386R, and V507I SLC4A11 mutations associated with corneal endothelial dystrophy affect the transporter function but not trafficking in PS120 cells (Q90585779) (← links)
- Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies (Q91622650) (← links)
- Slc4a11 disruption causes duct cell loss and impairs NaCl reabsorption in female mouse submandibular glands (Q91946288) (← links)
- ZEB1 insufficiency causes corneal endothelial cell state transition and altered cellular processing (Q92718830) (← links)
- Ammonia sensitive SLC4A11 mitochondrial uncoupling reduces glutamine induced oxidative stress (Q93122190) (← links)
- Phenotypic and functional characterization of corneal endothelial cells during in vitro expansion (Q94521487) (← links)
- Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation (Q98945076) (← links)