Hirtz S - Search Results

1

Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles.

Graeber SY, Vitzthum C, Pallenberg ST, Naehrlich L, Stahl M, Rohrbach A, Drescher M, Minso R, Ringshausen FC, Rueckes-Nilges C, Klajda J, Berges J, Yu Y, Scheuermann H, Hirtz S, Sommerburg O, Dittrich AM, Tümmler B, Mall MA. Graeber SY, et al. Among authors: hirtz s. Am J Respir Crit Care Med. 2022 Mar 1;205(5):540-549. doi: 10.1164/rccm.202110-2249OC. Am J Respir Crit Care Med. 2022. PMID: 34936849

2

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: hirtz s. 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.

3

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.

Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, Seydewitz HH, Yankaskas J, Kunzelmann K, Riordan JR, Boucher RC. Mall M, et al. Among authors: hirtz s. Gastroenterology. 2004 Jan;126(1):32-41. doi: 10.1053/j.gastro.2003.10.049. Gastroenterology. 2004. PMID: 14699484

4

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: hirtz s. 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.

5

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. Gastroenterology. 2004 Oct;127(4):1085-95. doi: 10.1053/j.gastro.2004.07.006. Gastroenterology. 2004. PMID: 15480987

6

Preventive but not late amiloride therapy reduces morbidity and mortality of lung disease in betaENaC-overexpressing mice.

Zhou Z, Treis D, Schubert SC, Harm M, Schatterny J, Hirtz S, Duerr J, Boucher RC, Mall MA. Zhou Z, et al. Among authors: hirtz s. Am J Respir Crit Care Med. 2008 Dec 15;178(12):1245-56. doi: 10.1164/rccm.200803-442OC. Epub 2008 Oct 10. Am J Respir Crit Care Med. 2008. PMID: 18849497

7

Allergic airway inflammation induces a pro-secretory epithelial ion transport phenotype in mice.

Anagnostopoulou P, Dai L, Schatterny J, Hirtz S, Duerr J, Mall MA. Anagnostopoulou P, et al. Among authors: hirtz s. Eur Respir J. 2010 Dec;36(6):1436-47. doi: 10.1183/09031936.00181209. Epub 2010 Apr 22. Eur Respir J. 2010. PMID: 20413543 Free article.

8

In vivo monitoring of cystic fibrosis-like lung disease in mice by volumetric computed tomography.

Wielpütz MO, Eichinger M, Zhou Z, Leotta K, Hirtz S, Bartling SH, Semmler W, Kauczor HU, Puderbach M, Mall MA. Wielpütz MO, et al. Among authors: hirtz s. Eur Respir J. 2011 Nov;38(5):1060-70. doi: 10.1183/09031936.00149810. Epub 2011 Apr 8. Eur Respir J. 2011. PMID: 21478215 Free article.

9

The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients.

Roth EK, Hirtz S, Duerr J, Wenning D, Eichler I, Seydewitz HH, Amaral MD, Mall MA. Roth EK, et al. Among authors: hirtz s. PLoS One. 2011;6(8):e24445. doi: 10.1371/journal.pone.0024445. Epub 2011 Aug 31. PLoS One. 2011. PMID: 21909392 Free PMC article.

10

CFTR regulates early pathogenesis of chronic obstructive lung disease in βENaC-overexpressing mice.

Johannesson B, Hirtz S, Schatterny J, Schultz C, Mall MA. Johannesson B, et al. Among authors: hirtz s. PLoS One. 2012;7(8):e44059. doi: 10.1371/journal.pone.0044059. Epub 2012 Aug 24. PLoS One. 2012. PMID: 22937152 Free PMC article.

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