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Classification of CFTR mutation classes.
Stanke F, Tümmler B. Stanke F, et al. Among authors: tummler b. Lancet Respir Med. 2016 Aug;4(8):e36. doi: 10.1016/S2213-2600(16)30147-3. Epub 2016 Jul 1. Lancet Respir Med. 2016. PMID: 27377412 No abstract available.
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe.
Dörk T, Macek M Jr, Mekus F, Tümmler B, Tzountzouris J, Casals T, Krebsová A, Koudová M, Sakmaryová I, Macek M Sr, Vávrová V, Zemková D, Ginter E, Petrova NV, Ivaschenko T, Baranov V, Witt M, Pogorzelski A, Bal J, Zékanowsky C, Wagner K, Stuhrmann M, Bauer I, Seydewitz HH, Neumann T, Jakubiczka S. Dörk T, et al. Among authors: tummler b. Hum Genet. 2000 Mar;106(3):259-68. doi: 10.1007/s004390000246. Hum Genet. 2000. PMID: 10798353
Basic protocol for transepithelial nasal potential difference measurements.
Schüler D, Sermet-Gaudelus I, Wilschanski M, Ballmann M, Dechaux M, Edelman A, Hug M, Leal T, Lebacq J, Lebecque P, Lenoir G, Stanke F, Wallemacq P, Tümmler B, Knowles MR. Schüler D, et al. Among authors: tummler b. J Cyst Fibros. 2004 Aug;3 Suppl 2:151-5. doi: 10.1016/j.jcf.2004.05.032. J Cyst Fibros. 2004. PMID: 15463949 Free article. Review.
Genetic modifiers in cystic fibrosis.
Stanke F, Tümmler B, Becker T. Stanke F, et al. Among authors: tummler b. N Engl J Med. 2006 Jan 5;354(1):88-90; author reply 88-90. doi: 10.1056/NEJMc052980. N Engl J Med. 2006. PMID: 16394309 No abstract available.
Ex vivo biochemical analysis of CFTR in human rectal biopsies.
van Barneveld A, Stanke F, Ballmann M, Naim HY, Tümmler B. van Barneveld A, et al. Among authors: tummler b. Biochim Biophys Acta. 2006 Apr;1762(4):393-7. doi: 10.1016/j.bbadis.2006.01.007. Epub 2006 Feb 13. Biochim Biophys Acta. 2006. PMID: 16504487 Free article.
367 results