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Seth L Alper

Showing results (181-190 of 258) with videos related to

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The Journal of Clinical Investigation|June 16, 2026
GLUT9b- and ABCG2-mediated collecting duct urate transport uncover a vasopressin-independent mechanism of renal water reabsorptionMohamad Hadla, Jean Marc Mardirossian, Daniel G Bichet, et al.
Journal of the American Society of Nephrology : JASN|March 2, 2022
DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk VariantsJustin Chun, Cristian V Riella, Hyunjae Chung, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Human Mutation|April 29, 2026
De Novo <i>TRIO</i> Missense Variants Disrupt Ras-GEF Domains and Cause Congenital Ventriculomegaly and HydrocephalusNeel H Mehta, Evan Dennis, Garrett Allington, et al.
American Journal of Physiology. Cell Physiology|May 16, 2019
Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cellsAlicia Rivera, David H Vandorpe, Boris E Shmukler, et al.
Frontiers in Physiology|July 10, 2015
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393WFabian R Reimold, Savithri Balasubramanian, David B Doroquez, et al.
Haematologica|June 10, 2021
A <i>Grammastola spatulata</i> mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologiesDavid H Vandorpe, Boris E Shmukler, Yann Ilboudo, et al.
Plos One|February 19, 2013
Transcriptional patterns in peritoneal tissue of encapsulating peritoneal sclerosis, a complication of chronic peritoneal dialysisFabian R Reimold, Niko Braun, Zsuzsanna K Zsengellér, et al.
Biology|October 27, 2022
Combined Treatment with KV Channel Inhibitor 4-Aminopyridine and either γ-Cystathionine Lyase Inhibitor β-Cyanoalanine or Epinephrine Restores Blood Pressure, and Improves Survival in the Wistar Rat Model of Anaphylactic ShockAbdelouahab Bellou, Nacira Sennoun, Elhadi H Aburawi, et al.
Pageof 26

Showing results (181-190 of 258) with videos related to

Sort By:
Pageof 26
The Journal of Clinical Investigation|June 16, 2026
GLUT9b- and ABCG2-mediated collecting duct urate transport uncover a vasopressin-independent mechanism of renal water reabsorptionMohamad Hadla, Jean Marc Mardirossian, Daniel G Bichet, et al.
Journal of the American Society of Nephrology : JASN|March 2, 2022
DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk VariantsJustin Chun, Cristian V Riella, Hyunjae Chung, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductTaku Ito, Byung Yoon Choi, Kelly A King, et al.
Human Mutation|April 29, 2026
De Novo <i>TRIO</i> Missense Variants Disrupt Ras-GEF Domains and Cause Congenital Ventriculomegaly and HydrocephalusNeel H Mehta, Evan Dennis, Garrett Allington, et al.
American Journal of Physiology. Cell Physiology|May 16, 2019
Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cellsAlicia Rivera, David H Vandorpe, Boris E Shmukler, et al.
Frontiers in Physiology|July 10, 2015
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393WFabian R Reimold, Savithri Balasubramanian, David B Doroquez, et al.
Haematologica|June 10, 2021
A <i>Grammastola spatulata</i> mechanotoxin-4 (GsMTx4)-sensitive cation channel mediates increased cation permeability in human hereditary spherocytosis of multiple genetic etiologiesDavid H Vandorpe, Boris E Shmukler, Yann Ilboudo, et al.
Plos One|February 19, 2013
Transcriptional patterns in peritoneal tissue of encapsulating peritoneal sclerosis, a complication of chronic peritoneal dialysisFabian R Reimold, Niko Braun, Zsuzsanna K Zsengellér, et al.
Biology|October 27, 2022
Combined Treatment with KV Channel Inhibitor 4-Aminopyridine and either γ-Cystathionine Lyase Inhibitor β-Cyanoalanine or Epinephrine Restores Blood Pressure, and Improves Survival in the Wistar Rat Model of Anaphylactic ShockAbdelouahab Bellou, Nacira Sennoun, Elhadi H Aburawi, et al.
Pageof 26