S. Verkaart

发表

TRPV5 Is Internalized via Clathrin-dependent Endocytosis to Enter a Ca2+-controlled Recycling Pathway*

U. Rescher, S. V. D. van de Graaf, J. Hoenderop, 2008, Journal of Biological Chemistry.

Inherited complex I deficiency is associated with faster protein diffusion in the matrix of moving mitochondria.

J. Fransen, J. Smeitink, M. Hink, 2008, American journal of physiology. Cell physiology.

Partial complex I inhibition decreases mitochondrial motility and increases matrix protein diffusion as revealed by fluorescence correlation spectroscopy.

J. Smeitink, M. Hink, P. Willems, 2007, Biochimica et biophysica acta.

The Na+/Ca2+ Exchanger 1 (NCX1) Variant 3 as the Major Extrusion System in Renal Distal Tubular Transcellular Ca2+-Transport

J. Hoenderop, S. Verkaart, R. Bindels, 2015, Nephron.

Interspecies differences in PTH-mediated PKA phosphorylation of the epithelial calcium channel TRPV5

M. Huynen, Teunis J. P. van Dam, S. Verkaart, 2017, Pflügers Archiv - European Journal of Physiology.

Cell Biological Consequences of OXPHOS Disorders

P. Willems, S. Verkaart, W. Koopman, 2004 .

Glucose specifically regulates TRPC6 expression in the podocyte in an AngII-dependent manner.

J. Wetzels, M. Baltissen, J. Hoenderop, 2014, The American journal of pathology.

CARDIOVASCULAR , PULMONARY , AND RENAL PATHOLOGY Glucose Speci fi cally Regulates TRPC 6 Expression in the Podocyte in an AngII-Dependent Manner

J. Wetzels, M. Baltissen, J. Hoenderop, 2022 .

Differential regulation of the Na+-Ca2+ exchanger 3 (NCX3) by protein kinase PKC and PKA.

J. Hoenderop, S. Verkaart, R. Bindels, 2017, Cell calcium.

Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy

S. Gallati, T. Slowinski, A. Schaller, 2012, Proceedings of the National Academy of Sciences.

β1-Adrenergic Receptor Signaling Activates the Epithelial Calcium Channel, Transient Receptor Potential Vanilloid Type 5 (TRPV5), via the Protein Kinase A Pathway*

J. Hoenderop, S. Verkaart, R. Bindels, 2014, The Journal of Biological Chemistry.

Tissue transglutaminase inhibits the TRPV5-dependent calcium transport in an N-glycosylation-dependent manner

J. Hoenderop, S. Verkaart, R. Bindels, 2012, Cellular and Molecular Life Sciences.

Role of the Transient Receptor Potential Vanilloid 5 (TRPV5) Protein N Terminus in Channel Activity, Tetramerization, and Trafficking*

V. te Boekhorst, J. Hoenderop, S. Verkaart, 2011, The Journal of Biological Chemistry.

3 as the Major Extrusion System in Renal Distal Tubular Transcellular Ca 2+ -Transport

J. Hoenderop, S. Verkaart, R. Bindels, 2015 .

Inhibition of Mitochondrial Na (cid:1) -Ca 2 (cid:1) Exchange Restores Agonist-induced ATP Production and Ca 2 (cid:1) Handling in Human Complex I Deficiency*

G. Rutter, J. Smeitink, L. P. Van den Heuvel, 2004 .

Cystine Dimethylester Model of Cystinosis: Still Reliable?

H. Blom, E. Levtchenko, L. Heuvel, 2007, Pediatric Research.

The calcium-sensing receptor promotes urinary acidification to prevent nephrolithiasis.

C. Wagner, A. Velic, J. Hoenderop, 2009, Journal of the American Society of Nephrology : JASN.

Flavaglines Stimulate Transient Receptor Potential Melastatin Type 6 (TRPM6) Channel Activity

J. Hoenderop, S. Verkaart, R. Bindels, 2015, PloS one.

A Novel Hypokalemic-Alkalotic Salt-Losing Tubulopathy in Patients with CLDN10 Mutations.

E. Bongers, J. Wetzels, S. Milatz, 2017, Journal of the American Society of Nephrology : JASN.

A primary culture of distal convoluted tubules expressing functional thiazide-sensitive NaCl transport.

J. Hoenderop, S. Verkaart, R. Bindels, 2012, American journal of physiology. Renal physiology.

A smart rhodamine-pyridine conjugate for bioimaging of thiocyanate in living cells†

K. Robeyns, A. Banerjee, S. Mandal, 2015 .

Mitochondrial and cytosolic thiol redox state are not detectably altered in isolated human NADH:ubiquinone oxidoreductase deficiency.

J. Smeitink, P. Willems, S. Verkaart, 2007, Biochimica et biophysica acta.

Human NADH:ubiquinone oxidoreductase deficiency: radical changes in mitochondrial morphology?

J. Smeitink, P. Willems, S. Verkaart, 2007, American journal of physiology. Cell physiology.

Cell biological consequences of inherited mitochondrial complex I deficiency : a radical study

S. Verkaart, 2007 .

Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiency.

J. Smeitink, P. Willems, S. Verkaart, 2008, Cell calcium.

Inhibition of complex I of the electron transport chain causes O2-. -mediated mitochondrial outgrowth.

F. H. van der Westhuizen, J. Smeitink, M. Murphy, 2005, American journal of physiology. Cell physiology.

Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5

Steve D. M. Brown, F. Ashcroft, R. Cox, 2013, PloS one.

Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly.

Rutger O. Vogel, J. Smeitink, L. P. Van den Heuvel, 2007, Genes & development.

Nucleolin associates with a subset of the human Ro ribonucleoprotein complexes.

G. Pruijn, W. V. van Venrooij, P. Bouvet, 2002, Journal of molecular biology.

Superoxide production is inversely related to complex I activity in inherited complex I deficiency.

J. Smeitink, P. Willems, S. Verkaart, 2007, Biochimica et biophysica acta.

Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency.

J. Smeitink, P. Willems, S. Verkaart, 2005, American journal of physiology. Cell physiology.

Mitigation of NADH: ubiquinone oxidoreductase deficiency by chronic Trolox treatment.

J. Smeitink, P. Willems, S. Verkaart, 2008, Biochimica et biophysica acta.

Simultaneous quantification of oxidative stress and cell spreading using 5‐(and‐6)‐chloromethyl‐2′,7′‐dichlorofluorescein

J. Smeitink, P. Willems, S. Verkaart, 2006, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

Urinary plasmin inhibits TRPV5 in nephrotic-range proteinuria.

G. Navis, A. Kwakernaak, N. Kovalevskaya, 2012, Journal of the American Society of Nephrology : JASN.

A de novo KCNA1 Mutation in a Patient with Tetany and Hypomagnesemia

M. Konrad, M. Tkaczyk, J. Altmüller, 2018, Nephron.

Functionomics of NCC mutations in Gitelman syndrome using a novel mammalian cell-based activity assay.

Á. Valdez-Ortiz, J. Hoenderop, S. Verkaart, 2016, American journal of physiology. Renal physiology.

Function and Regulation of the Na+-Ca2+ Exchanger NCX3 Splice Variants in Brain and Skeletal Muscle*

P. Willems, J. Hoenderop, S. Verkaart, 2014, The Journal of Biological Chemistry.

Function and Regulation of the Na -Ca Exchanger NCX3 Splice Variants in Brain and Skeletal Muscle*

P. Willems, J. Hoenderop, S. Verkaart, 2014 .

Molecular Mechanisms of Calmodulin Action on TRPV5 and Modulation by Parathyroid Hormone

G. W. Vuister, N. Kovalevskaya, J. Hoenderop, 2011, Molecular and Cellular Biology.

The Identification of Histidine 712 as a Critical Residue for Constitutive TRPV5 Internalization*

J. Hoenderop, S. Verkaart, R. Bindels, 2010, The Journal of Biological Chemistry.