Hedtfeld S - Search Results

1

Nasal potential difference of carriers of the W493R ENaC variant with non-cystic fibrosis bronchiectasis.

Rademacher J, Schulz A, Hedtfeld S, Stanke F, Ringshausen F, Welte T, Tümmler B. Rademacher J, et al. Among authors: hedtfeld s. Eur Respir J. 2016 Jan;47(1):322-4. doi: 10.1183/13993003.01128-2015. Epub 2015 Oct 9. Eur Respir J. 2016. PMID: 26453628 Free article. No abstract available.

2

Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.

Stanke F, Becker T, Hedtfeld S, Tamm S, Wienker TF, Tümmler B. Stanke F, et al. Among authors: hedtfeld s. Hum Genet. 2010 Apr;127(4):383-94. doi: 10.1007/s00439-009-0779-6. Epub 2010 Jan 3. Hum Genet. 2010. PMID: 20047061

3

Differential decay of parent-of-origin-specific genomic sharing in cystic fibrosis-affected sib pairs maps a paternally imprinted locus to 7q34.

Stanke F, Davenport C, Hedtfeld S, Tümmler B. Stanke F, et al. Among authors: hedtfeld s. Eur J Hum Genet. 2010 May;18(5):553-9. doi: 10.1038/ejhg.2009.229. Epub 2010 Jan 6. Eur J Hum Genet. 2010. PMID: 20051989 Free PMC article.

4

Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia.

Stanke F, Becker T, Kumar V, Hedtfeld S, Becker C, Cuppens H, Tamm S, Yarden J, Laabs U, Siebert B, Fernandez L, Macek M Jr, Radojkovic D, Ballmann M, Greipel J, Cassiman JJ, Wienker TF, Tümmler B. Stanke F, et al. Among authors: hedtfeld s. J Med Genet. 2011 Jan;48(1):24-31. doi: 10.1136/jmg.2010.080937. Epub 2010 Sep 12. J Med Genet. 2011. PMID: 20837493 Free PMC article.

5

An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion.

Stanke F, Hedtfeld S, Becker T, Tümmler B. Stanke F, et al. Among authors: hedtfeld s. BMC Med Genet. 2011 May 6;12:62. doi: 10.1186/1471-2350-12-62. BMC Med Genet. 2011. PMID: 21548936 Free PMC article.

6

Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation.

Labenski H, Hedtfeld S, Becker T, Tümmler B, Stanke F. Labenski H, et al. Among authors: hedtfeld s. Eur J Hum Genet. 2011 Dec;19(12):1281-8. doi: 10.1038/ejhg.2011.129. Epub 2011 Jul 6. Eur J Hum Genet. 2011. PMID: 21731057 Free PMC article.

7

Frequency of the hyperactive W493R ENaC variant in carriers of a CFTR mutation.

Handschick M, Hedtfeld S, Tümmler B. Handschick M, et al. Among authors: hedtfeld s. J Cyst Fibros. 2012 Jan;11(1):53-5. doi: 10.1016/j.jcf.2011.08.008. Epub 2011 Sep 13. J Cyst Fibros. 2012. PMID: 21917531 Free article.

8

Effective prevention of Pseudomonas aeruginosa cross-infection at a cystic fibrosis centre - results of a 10-year prospective study.

Wiehlmann L, Cramer N, Ulrich J, Hedtfeld S, Weissbrodt H, Tümmler B. Wiehlmann L, et al. Among authors: hedtfeld s. Int J Med Microbiol. 2012 Mar;302(2):69-77. doi: 10.1016/j.ijmm.2011.11.001. Epub 2011 Dec 22. Int J Med Microbiol. 2012. PMID: 22196973

9

CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestine.

Kolbe EW, Tamm S, Hedtfeld S, Becker T, Tümmler B, Stanke F. Kolbe EW, et al. Among authors: hedtfeld s. Eur J Hum Genet. 2013 Jun;21(6):691-4. doi: 10.1038/ejhg.2012.234. Epub 2012 Oct 17. Eur J Hum Genet. 2013. PMID: 23073314 Free PMC article.

10

The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells.

Stanke F, van Barneveld A, Hedtfeld S, Wölfl S, Becker T, Tümmler B. Stanke F, et al. Among authors: hedtfeld s. Eur J Hum Genet. 2014 May;22(5):660-6. doi: 10.1038/ejhg.2013.209. Epub 2013 Oct 9. Eur J Hum Genet. 2014. PMID: 24105369 Free PMC article.

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