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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
Authors: Karschin, C.; Wischmeyer, E.; Preisig-Mueller, R.; Rajan, S.; Derst, C.; Grzeschik, K. H.; Daut, J.; Karschin, A.
Date of Publication (YYYY-MM-DD): 2001-12
Title of Journal: Molecular and Cellular Neuroscience
Volume: 18
Issue / Number: 6
Start Page: 632
End Page: 648
Document Type: Article
ID: 233178.0


TASK-3, a novel tandem pore domain acid-sensitive K+ channel.
Authors: Rajan, S.; Wischmeyer, E.; Liu, G. X.; Preisig-Mueller, R.; Daut, J.; Karschin, A.; Derst, C.
Date of Publication (YYYY-MM-DD): 2000
Title of Journal: Journal of Biological Chemistry
Volume: 275
Start Page: 16650
End Page: 16657
Document Type: Article
ID: 233711.0


Cloning, structure and assignment to Chromosome 19q13 of the human Kir2.4 inwardly rectifying potassium channel gene (KCNJ 14)
Authors: Toepert, C.; Doering, F.; Derst, C.; Daut, J.; Grzeschik, K. H.; Karschin, A.
Date of Publication (YYYY-MM-DD): 2000
Title of Journal: Mammalian Genome
Volume: 11
Start Page: 247
End Page: 249
Document Type: Article
ID: 240141.0


The epithelial inward rectifier channel Kir7.1 displays unusual K+ permeation properties.
Authors: Doering, F.; Derst, C.; Wischmeyer, E.; Karschin, C.; Schneggenburger, R.; Daut, J.; Karschin, A.
Date of Publication (YYYY-MM-DD): 1998
Title of Journal: Journal of Neuroscience
Volume: 18
Start Page: 8625
End Page: 8636
Document Type: Article
ID: 224515.0


Gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel Kir 7.1 (KCNJ13).
Authors: Derst, C.; Doering, F.; Preisig-Mueller, R.; Daut, J.; Karschin, A.; Jeck, N.; Weber, S.; Engel, H.; Grzeschik, K. H.
Date of Publication (YYYY-MM-DD): 1998
Title of Journal: Genomics
Volume: 54
Start Page: 560
End Page: 563
Document Type: Article
ID: 233193.0


A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels.
Authors: Derst, C.; Wischmeyer, E.; Preisig-Mueller, R.; Spauschus, A.; Konrad, M.; Hensen, P.; Jeck, N.; Seyberth, H. W.; Daut, J.; Karschin, A.
Date of Publication (YYYY-MM-DD): 1998
Title of Journal: Journal of Biological Chemistry
Volume: 273
Start Page: 23884
End Page: 23891
Document Type: Article
ID: 233195.0


Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function
Authors: Derst, C.; Konrad, M.; Kockerling, A.; Karolyi, L.; Deschenes, G.; Daut, J.; Karschin, A.; Seyberth, H. W.
Date of Publication (YYYY-MM-DD): 1997-01-23
Title of Journal: Biochemical and Biophysical Research Communications
Volume: 230
Issue / Number: 3
Start Page: 641
End Page: 645
Document Type: Article
ID: 260944.0