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Year | Number of Results |
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2013 | 1 |
2014 | 1 |
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PubMed for id: 4844
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Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations.
Genes (Basel). 2021 Sep 29;12(10):1554. doi: 10.3390/genes12101554.
Genes (Basel). 2021.
PMID: 34680949
Free PMC article.
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.
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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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.
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.
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