S. Bandulik

发表

KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function

Markus Rapedius, R. Witzgall, R. Kleta, 2010, Proceedings of the National Academy of Sciences.

Task3 potassium channel gene invalidation causes low renin and salt-sensitive arterial hypertension.

E. Lalli, J. Barhanin, T. Budde, 2012, Endocrinology.

The calcium-activated chloride channel Anoctamin 1 contributes to the regulation of renal function.

R. Witzgall, H. Pavenstädt, R. Schreiber, 2014, Kidney international.

ApoA-I induces a preferential efflux of monounsaturated phosphatidylcholine and medium chain sphingomyelin species from a cellular pool distinct from HDL(3) mediated phospholipid efflux.

T. Langmann, G. Schmitz, G. Liebisch, 2007, Biochimica et biophysica acta.

Ezetimib influences the expression of raft‐associated antigens in human monocytes†

G. Schmitz, S. Bandulik, T. Werner, 2006, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability.

M. Tarailo-Graovac, C. V. van Karnebeek, Jessica J. Y. Lee, 2018, American journal of human genetics.

Severe hyperaldosteronism in neonatal Task3 potassium channel knockout mice is associated with activation of the intraadrenal renin-angiotensin system.

E. Lalli, J. Barhanin, Michael Hartmann, 2013, Endocrinology.

Zinc transporter somatic gene mutations cause primary aldosteronism

T. Giordano, H. Sasano, C. Kumar-Sinha, 2022, bioRxiv.

Pathogenesis of Adrenal Aldosterone-Producing Adenomas Carrying Mutations of the Na(+)/K(+)-ATPase.

S. Bandulik, C. Sterner, I. Tegtmeier, 2015, Endocrinology.

KCNJ5 Mutations in European Families With Nonglucocorticoid Remediable Familial Hyperaldosteronism

T. Strom, F. Beuschlein, X. Jeunemaître, 2012, Hypertension.

Cellular pathophysiology of mutant voltage-dependent Ca2+ channel CACNA1H in primary aldosteronism.

S. Bandulik, I. Tegtmeier, R. Warth, 2020, Endocrinology.

Two-pore domain potassium channels in the adrenal cortex

E. Lalli, J. Barhanin, S. Bandulik, 2014, Pflügers Archiv - European Journal of Physiology.

Potassium channels in adrenocortical cells

J. Barhanin, S. Bandulik, R. Warth, 2019, Current Opinion in Endocrine and Metabolic Research.

TASK1 and TASK3 Potassium Channels: Determinants of Aldosterone Secretion and Adrenocortical Zonation

J. Barhanin, S. Bandulik, D. Pentón, 2010, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.

Dorothy A. Thompson, M. Hubank, J. Cross, 2009, The New England journal of medicine.

Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis

W. Wisden, E. Lalli, S. Bendahhou, 2008, The EMBO journal.

A case of severe hyperaldosteronism caused by a de novo mutation affecting a critical salt bridge Kir3.4 residue.

C. Stratakis, P. Mulatero, S. Monticone, 2015, The Journal of clinical endocrinology and metabolism.

Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex.

C. Niehrs, E. Lalli, S. Bendahhou, 2012, Human molecular genetics.

Cellular Pathophysiology of an Adrenal Adenoma-Associated Mutant of the Plasma Membrane Ca(2+)-ATPase ATP2B3.

F. Beuschlein, S. Bandulik, R. Warth, 2016, Endocrinology.

The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel

R. Kleta, M. Reichold, A. Zdebik, 2011, Pflügers Archiv - European Journal of Physiology.

Task2 potassium channels set central respiratory CO2 and O2 sensitivity

P. Pierson, M. Georgieff, S. Bendahhou, 2010, Proceedings of the National Academy of Sciences.

Collecting system-specific deletion of Kcnj10 predisposes for thiazide- and low-potassium diet-induced hypokalemia.

J. Loffing, A. Forst, S. Bandulik, 2020, Kidney international.

Dynamics of Renal Electrolyte Excretion in Growing Mice

M. Reichold, Katharina Schmidt, S. Bandulik, 2013, Nephron Physiology.

Of channels and pumps: different ways to boost the aldosterone?

S. Bandulik, 2017, Acta physiologica.

A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassium.

V. Fishman, C. Gomez-Sanchez, G. Zanotti, 2014, The Journal of clinical endocrinology and metabolism.

Pharmacology and pathophysiology of mutated KCNJ5 found in adrenal aldosterone-producing adenomas.

F. Beuschlein, J. Barhanin, S. Bandulik, 2014, Endocrinology.

Rare but Relevant Kidney Disorders

Knepper, Dorothy A. Thompson, M. Hubank, 2009, Clinical Journal of the American Society of Nephrology.

Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronism

A. Turcu, S. Bandulik, R. Warth, 2023, Nature Genetics.

KCNJ5 Mutations in European Families With Nonglucocorticoid Remediable Familial Hyperaldosteronism

T. Strom, F. Beuschlein, X. Jeunemaître, 2012, Hypertension.

Cellular Pathophysiology of an Adrenal Adenoma-Associated Mutant of the Plasma Membrane Ca(2+)-ATPase ATP2B3.

S. Bandulik, P. Tauber, Y. Rhayem, 2016, Endocrinology.