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Beta-actin is a target for transglutaminase activity at synaptic endings in chicken telencephalic cell cultures.
Dolge L, Aufenvenne K, Traupe H, Baumgartner W. Dolge L, et al. Among authors: traupe h. J Mol Neurosci. 2012 Feb;46(2):410-9. doi: 10.1007/s12031-011-9601-8. Epub 2011 Jul 26. J Mol Neurosci. 2012. PMID: 21789544
A novel in situ method for the detection of deficient transglutaminase activity in the skin.
Raghunath M, Hennies HC, Velten F, Wiebe V, Steinert PM, Reis A, Traupe H. Raghunath M, et al. Among authors: traupe h. Arch Dermatol Res. 1998 Nov;290(11):621-7. doi: 10.1007/s004030050362. Arch Dermatol Res. 1998. PMID: 9860283
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
Oji V, Seller N, Sandilands A, Gruber R, Gerss J, Hüffmeier U, Hamm H, Emmert S, Aufenvenne K, Metze D, Luger T, Loser K, Hausser I, Traupe H, McLean WH. Oji V, et al. Among authors: traupe h. Br J Dermatol. 2009 Apr;160(4):771-81. doi: 10.1111/j.1365-2133.2008.08999.x. Epub 2009 Jan 13. Br J Dermatol. 2009. PMID: 19183181
Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1.
Oji V, Oji ME, Adamini N, Walker T, Aufenvenne K, Raghunath M, Traupe H. Oji V, et al. Among authors: traupe h. Br J Dermatol. 2006 May;154(5):860-7. doi: 10.1111/j.1365-2133.2005.07109.x. Br J Dermatol. 2006. PMID: 16634887
Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko.
Traupe H. Traupe H. Am J Med Genet. 1999 Aug 6;85(4):324-9. doi: 10.1002/(sici)1096-8628(19990806)85:4<324::aid-ajmg2>;2-o. Am J Med Genet. 1999. PMID: 10398252
Unstable pre-mutation may explain mosaic disease expression of incontinentia pigmenti in males.
Traupe H, Vehring KH. Traupe H, et al. Am J Med Genet. 1994 Feb 15;49(4):397-8. doi: 10.1002/ajmg.1320490409. Am J Med Genet. 1994. PMID: 8160732
Hereditary angioedema with normal C1-inhibitor activity in women.
Bork K, Barnstedt SE, Koch P, Traupe H. Bork K, et al. Among authors: traupe h. Lancet. 2000 Jul 15;356(9225):213-7. doi: 10.1016/S0140-6736(00)02483-1. Lancet. 2000. PMID: 10963200
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicism.
Has C, Bruckner-Tuderman L, Müller D, Floeth M, Folkers E, Donnai D, Traupe H. Has C, et al. Among authors: traupe h. Hum Mol Genet. 2000 Aug 12;9(13):1951-5. doi: 10.1093/hmg/9.13.1951. Hum Mol Genet. 2000. PMID: 10942423
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease.
Oji V, Eckl KM, Aufenvenne K, Nätebus M, Tarinski T, Ackermann K, Seller N, Metze D, Nürnberg G, Fölster-Holst R, Schäfer-Korting M, Hausser I, Traupe H, Hennies HC. Oji V, et al. Among authors: traupe h. Am J Hum Genet. 2010 Aug 13;87(2):274-81. doi: 10.1016/j.ajhg.2010.07.005. Am J Hum Genet. 2010. PMID: 20691404 Free PMC article.
The expression of the 27-kd heat shock protein in keratinization disorders: an immunohistological study.
Jonak C, Metze D, Traupe H, Happle R, König A, Trautinger F. Jonak C, et al. Among authors: traupe h. Hum Pathol. 2005 Jun;36(6):686-93. doi: 10.1016/j.humpath.2005.04.009. Hum Pathol. 2005. PMID: 16021576
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