Gonska T - Search Results

1

Na(+)-dependent and -independent amino acid transport systems in immortalized human kidney epithelial cells derived from the proximal tubule.

Hirsch JR, Gonska T, Waldegger S, Lang F, Schlatter E. Hirsch JR, et al. Among authors: gonska t. Kidney Blood Press Res. 1998;21(1):50-8. doi: 10.1159/000025843. Kidney Blood Press Res. 1998. PMID: 9661137

2

Amino acid transport in the renal proximal tubule.

Gonska T, Hirsch JR, Schlatter E. Gonska T, et al. Amino Acids. 2000;19(2):395-407. doi: 10.1007/s007260070019. Amino Acids. 2000. PMID: 11128548 Review.

3

Diadenosine polyphosphates activate a Ca(2+)-dependent K(+)-conductance in porcine aortic smooth muscle cells via P2-purinoceptors.

Schlatter E, Gonska T, Windau J, Mehrens T. Schlatter E, et al. Among authors: gonska t. Cell Physiol Biochem. 2000;10(3):125-34. doi: 10.1159/000016343. Cell Physiol Biochem. 2000. PMID: 10878443

4

Inhibition of amiloride-sensitive epithelial Na(+) absorption by extracellular nucleotides in human normal and cystic fibrosis airways.

Mall M, Wissner A, Gonska T, Calenborn D, Kuehr J, Brandis M, Kunzelmann K. Mall M, et al. Among authors: gonska t. Am J Respir Cell Mol Biol. 2000 Dec;23(6):755-61. doi: 10.1165/ajrcmb.23.6.4207. Am J Respir Cell Mol Biol. 2000. PMID: 11104728

5

A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene.

Seydewitz HH, Gonska T, Mall M, Kueh J. Seydewitz HH, et al. Among authors: gonska t. Hum Mutat. 2000 Sep;16(3):277. doi: 10.1002/1098-1004(200009)16:3<277::AID-HUMU26>3.0.CO;2-S. Hum Mutat. 2000. PMID: 10980550 No abstract available.

6

Transcript analysis of the cystic fibrosis splicing mutation 1525-1G>A shows use of multiple alternative splicing sites and suggests a putative role of exonic splicing enhancers.

Ramalho AS, Beck S, Penque D, Gonska T, Seydewitz HH, Mall M, Amaral MD. Ramalho AS, et al. Among authors: gonska t. J Med Genet. 2003 Jul;40(7):e88. doi: 10.1136/jmg.40.7.e88. J Med Genet. 2003. PMID: 12843337 Free PMC article. No abstract available.

7

Activation of ion secretion via proteinase-activated receptor-2 in human colon.

Mall M, Gonska T, Thomas J, Hirtz S, Schreiber R, Kunzelmann K. Mall M, et al. Among authors: gonska t. Am J Physiol Gastrointest Liver Physiol. 2002 Feb;282(2):G200-10. doi: 10.1152/ajpgi.00137.2001. Am J Physiol Gastrointest Liver Physiol. 2002. PMID: 11804840 Free article.

8

Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia.

Mall M, Gonska T, Thomas J, Schreiber R, Seydewitz HH, Kuehr J, Brandis M, Kunzelmann K. Mall M, et al. Among authors: gonska t. Pediatr Res. 2003 Apr;53(4):608-18. doi: 10.1203/01.PDR.0000057204.51420.DC. Epub 2003 Feb 5. Pediatr Res. 2003. PMID: 12612194

9

Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis.

Mall M, Hirtz S, Gonska T, Kunzelmann K. Mall M, et al. Among authors: gonska t. J Cyst Fibros. 2004 Aug;3 Suppl 2:165-9. doi: 10.1016/j.jcf.2004.05.035. J Cyst Fibros. 2004. PMID: 15463952 Free article. Review.

10

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M. Hirtz S, et al. Among authors: gonska t. Gastroenterology. 2004 Oct;127(4):1085-95. doi: 10.1053/j.gastro.2004.07.006. Gastroenterology. 2004. PMID: 15480987

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