Karschin, C., E. Wischmeyer, R. Preisig-Mueller, S. Rajan, C. Derst, K. H. Grzeschik, J. Daut and A. Karschin: Expression pattern in brain of TASK-1, TASK-3, and a tandem pore domain K+ channel subunit, TASK-5, associated with the central auditory nervous system. In: Molecular and Cellular Neuroscience 18, 6, 632-648 (2001).
url: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WNB-456JPMM-5-1&_cdi=6958&_user=38661&_pii=S1044743101910450&_origin=search&_coverDate=12%2F31%2F2001&_sk=999819993&view=c&wchp=dGLbVtz-zSkzk&md5=b9a83a8cbe4d1cf29341b4ca00718c3a&ie=/sdarticle.pdf
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Toepert, C., F. Doering, C. Derst, J. Daut, K. H. Grzeschik and A. Karschin: Cloning, structure and assignment to Chromosome 19q13 of the human Kir2.4 inwardly rectifying potassium channel gene (KCNJ 14). In: Mammalian Genome 11, 247-249 (2000).
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Doering, F., C. Derst, E. Wischmeyer, C. Karschin, R. Schneggenburger, J. Daut and A. Karschin: The epithelial inward rectifier channel Kir7.1 displays unusual K+ permeation properties.. In: Journal of Neuroscience 18, 8625-8636 (1998).
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Derst, C., F. Doering, R. Preisig-Mueller, J. Daut, A. Karschin, N. Jeck, S. Weber, H. Engel and K. H. Grzeschik: Gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel Kir 7.1 (KCNJ13).. In: Genomics 54, 560-563 (1998).
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Derst, C., E. Wischmeyer, R. Preisig-Mueller, A. Spauschus, M. Konrad, P. Hensen, N. Jeck, H. W. Seyberth, J. Daut and A. Karschin: A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels.. In: Journal of Biological Chemistry 273, 23884-23891 (1998).
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Derst, C., M. Konrad, A. Kockerling, L. Karolyi, G. Deschenes, J. Daut, A. Karschin and H. W. Seyberth: Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function. In: Biochemical and Biophysical Research Communications 230, 3, 641-645 (1997).
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