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Enriko Klootwijk

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 20, 2011
Filtering the genes and sorting the glomerular filter: a new piece in the puzzle?Robert Kleta, Enriko Klootwijk, Horia Stanescu, et al.
World Journal of Nephrology|February 4, 2022
Literature review of the mechanisms of acute kidney injury secondary to acute liver injuryEsther Platt, Enriko Klootwijk, Alan Salama, et al.
Lancet (London, England)|January 7, 2014
A novel claudin-16 mutation, severe bone disease, and nephrocalcinosisLuxme Nadarajah, Maryam Khosravi, Simona Dumitriu, et al.
European Journal of Clinical Investigation|February 13, 2013
ATP and arterial calcificationRichard S Fish, Enriko Klootwijk, Frederick W K Tam, et al.
Molecular Genetics and Metabolism|March 31, 2010
OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondriaMarjan Huizing, Heidi Dorward, Lien Ly, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
Frontiers in Cell and Developmental Biology|October 30, 2023
A missense mutation in <i>Ehd1</i> associated with defective spermatogenesis and male infertilityKatrin Meindl, Naomi Issler, Sara Afonso, et al.
Nephron. Physiology|November 7, 2013
KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16Sophie Parrock, Sofia Hussain, Naomi Issler, et al.
The New England Journal of Medicine|May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsDetlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 20, 2011
Filtering the genes and sorting the glomerular filter: a new piece in the puzzle?Robert Kleta, Enriko Klootwijk, Horia Stanescu, et al.
World Journal of Nephrology|February 4, 2022
Literature review of the mechanisms of acute kidney injury secondary to acute liver injuryEsther Platt, Enriko Klootwijk, Alan Salama, et al.
Lancet (London, England)|January 7, 2014
A novel claudin-16 mutation, severe bone disease, and nephrocalcinosisLuxme Nadarajah, Maryam Khosravi, Simona Dumitriu, et al.
European Journal of Clinical Investigation|February 13, 2013
ATP and arterial calcificationRichard S Fish, Enriko Klootwijk, Frederick W K Tam, et al.
Molecular Genetics and Metabolism|March 31, 2010
OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondriaMarjan Huizing, Heidi Dorward, Lien Ly, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
Frontiers in Cell and Developmental Biology|October 30, 2023
A missense mutation in <i>Ehd1</i> associated with defective spermatogenesis and male infertilityKatrin Meindl, Naomi Issler, Sara Afonso, et al.
Nephron. Physiology|November 7, 2013
KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16Sophie Parrock, Sofia Hussain, Naomi Issler, et al.
The New England Journal of Medicine|May 8, 2009
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutationsDetlef Bockenhauer, Sally Feather, Horia C Stanescu, et al.
Pageof 2