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Complement activating antibodies to myelin oligodendrocyte glycoprotein in neuromyelitis optica and related disorders.
Mader S, Gredler V, Schanda K, Rostasy K, Dujmovic I, Pfaller K, Lutterotti A, Jarius S, Di Pauli F, Kuenz B, Ehling R, Hegen H, Deisenhammer F, Aboul-Enein F, Storch MK, Koson P, Drulovic J, Kristoferitsch W, Berger T, Reindl M. Mader S, et al. Among authors: pfaller k. J Neuroinflammation. 2011 Dec 28;8:184. doi: 10.1186/1742-2094-8-184. J Neuroinflammation. 2011. PMID: 22204662 Free PMC article.
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity.
Müller T, Hess MW, Schiefermeier N, Pfaller K, Ebner HL, Heinz-Erian P, Ponstingl H, Partsch J, Röllinghoff B, Köhler H, Berger T, Lenhartz H, Schlenck B, Houwen RJ, Taylor CJ, Zoller H, Lechner S, Goulet O, Utermann G, Ruemmele FM, Huber LA, Janecke AR. Müller T, et al. Among authors: pfaller k. Nat Genet. 2008 Oct;40(10):1163-5. doi: 10.1038/ng.225. Epub 2008 Aug 24. Nat Genet. 2008. PMID: 18724368
Nogo-A expression in the brain of mice with cerebral malaria.
Lackner P, Beer R, Broessner G, Helbok R, Dallago K, Hess MW, Pfaller K, Bandtlow C, Schmutzhard E. Lackner P, et al. Among authors: pfaller k. PLoS One. 2011;6(9):e25728. doi: 10.1371/journal.pone.0025728. Epub 2011 Sep 29. PLoS One. 2011. PMID: 21980529 Free PMC article.
The viral make-up makes a world of difference.
Posch W, Pfaller K, Lass-Flörl C, Wilflingseder D. Posch W, et al. Among authors: pfaller k. AIDS Res Hum Retroviruses. 2014 Jul;30(7):642-3. doi: 10.1089/aid.2014.0061. AIDS Res Hum Retroviruses. 2014. PMID: 24984236 No abstract available.
Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model.
Ruemmele FM, Müller T, Schiefermeier N, Ebner HL, Lechner S, Pfaller K, Thöni CE, Goulet O, Lacaille F, Schmitz J, Colomb V, Sauvat F, Revillon Y, Canioni D, Brousse N, de Saint-Basile G, Lefebvre J, Heinz-Erian P, Enninger A, Utermann G, Hess MW, Janecke AR, Huber LA. Ruemmele FM, et al. Among authors: pfaller k. Hum Mutat. 2010 May;31(5):544-51. doi: 10.1002/humu.21224. Hum Mutat. 2010. PMID: 20186687
Towards understanding microvillus inclusion disease.
Vogel GF, Hess MW, Pfaller K, Huber LA, Janecke AR, Müller T. Vogel GF, et al. Among authors: pfaller k. Mol Cell Pediatr. 2016 Dec;3(1):3. doi: 10.1186/s40348-016-0031-0. Epub 2016 Jan 29. Mol Cell Pediatr. 2016. PMID: 26830108 Free PMC article.
Loss of syntaxin 3 causes variant microvillus inclusion disease.
Wiegerinck CL, Janecke AR, Schneeberger K, Vogel GF, van Haaften-Visser DY, Escher JC, Adam R, Thöni CE, Pfaller K, Jordan AJ, Weis CA, Nijman IJ, Monroe GR, van Hasselt PM, Cutz E, Klumperman J, Clevers H, Nieuwenhuis EE, Houwen RH, van Haaften G, Hess MW, Huber LA, Stapelbroek JM, Müller T, Middendorp S. Wiegerinck CL, et al. Among authors: pfaller k. Gastroenterology. 2014 Jul;147(1):65-68.e10. doi: 10.1053/j.gastro.2014.04.002. Epub 2014 Apr 12. Gastroenterology. 2014. PMID: 24726755
114 results