Results
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Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome. [electronic resource] by
- Jeck, N
- Derst, C
- Wischmeyer, E
- Ott, H
- Weber, S
- Rudin, C
- Seyberth, H W
- Daut, J
- Karschin, A
- Konrad, M
Producer: 20010726
In:
Kidney international vol. 59
Availability: No items available.
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Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits. [electronic resource] by
- Derst, C
- Karschin, C
- Wischmeyer, E
- Hirsch, J R
- Preisig-Müller, R
- Rajan, S
- Engel, H
- Grzeschik, K
- Daut, J
- Karschin, A
Producer: 20010419
In:
FEBS letters vol. 491
Availability: No items available.
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28.
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A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels. [electronic resource] by
- Derst, C
- Wischmeyer, E
- Preisig-Müller, R
- Spauschus, A
- Konrad, M
- Hensen, P
- Jeck, N
- Seyberth, H W
- Daut, J
- Karschin, A
Producer: 19981013
In:
The Journal of biological chemistry vol. 273
Availability: No items available.
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29.
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Cellular localization of the potassium channel Kir7.1 in guinea pig and human kidney. [electronic resource] by
- Derst, C
- Hirsch, J R
- Preisig-Müller, R
- Wischmeyer, E
- Karschin, A
- Döring, F
- Thomzig, A
- Veh, R W
- Schlatter, E
- Kummer, W
- Daut, J
Producer: 20010809
In:
Kidney international vol. 59
Availability: No items available.
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