Melanie Peters
Publications by Year
Research Areas
Ion Transport and Channel Regulation, Ion channel regulation and function, Magnesium in Health and Disease, Pharmacogenetics and Drug Metabolism, Metabolomics and Mass Spectrometry Studies
Most-Cited Works
- → Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family(2002)776 cited
- → Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis(2001)270 cited
- → Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies(2002)261 cited
- → Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype(2000)194 cited
- → Barttin increases surface expression and changes current properties of ClC-K channels(2002)171 cited
- → Salt handling in the distal nephron: lessons learned from inherited human disorders(2005)122 cited
- → Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome(2003)76 cited
- → Studies on trans-cinnamaldehyde. I. The influence of dose size and sex on its disposition in the rat and mouse(1994)54 cited
- → Cytotoxicity and cell-proliferation induced by the nephrocarcinogen hydroquinone and its nephrotoxic metabolite 2,3,5-(tris-glutathion-S- yl)hydroquinone(1997)53 cited
- Glutathione conjugates of tert-butyl-hydroquinone, a metabolite of the urinary tract tumor promoter 3-tert-butyl-hydroxyanisole, are toxic to kidney and bladder.(1996)