Universität zu Köln

University / College


Location: Köln, Germany (DE) DE

ISNI: 0000000085803777

ROR: https://ror.org/00rcxh774

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta (2012) Tagariello A, Breuer C, Birkner Y, Schmidt S, Koch AM, Cesnjevar R, Rueffer A, et al. Journal article Trastuzumab beyond progression: Overall survival analysis of the GBG 26/BIG 3-05 phase III study in HER2-positive breast cancer (2011) Von Minckwitz G, Schweller K, Schmidt M, Barinoff J, Mundhenke C, Cufer T, Maartense E, et al. Journal article Do locked compression intramedullary nails improve the biomechanical stability of distal femoral fractures? (2011) Wild M, Thelen S, Spoor V, Eichler C, Koebke J, Jungbluth P, Betsch M, et al. Journal article Via Minimization in VLSI Chip Design - Application of a Planar Max-Cut Algorithm (2011) Liers F, Nieberg T, Pardella GL Other publication type, Preprint Fetal programming of gene expression in growth-restricted rats depends on the cause of low birth weight (2011) Nuesken KD, Schneider H, Plank CG, Trollmann R, Nuesken E, Rascher W, Doetsch J Journal article Inhibition of tgf-β signaling and decreased apoptosis in iugr-associated lung disease in rats (2011) Alcazar MAA, Morty RE, Lendzian L, Vohlen C, Oestreicher I, Plank CG, Schneider H, Doetsch J Journal article Geschichte der Ästhetischen Bildung Band 2 - Frühe Neuzeit (2011) Klepacki L, Zirfas J Authored book Simplifying maximum flow computations: The effect of shrinking and good initial flows (2011) Liers F, Pardella GL Journal article, Original article An exact algorithm for robust network design (2011) Buchheim C, Liers F, Sanità L Book chapter / Article in edited volumes Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome (2011) Krumbiegel M, Pasutto F, Schlötzer-Schrehardt U, Uebe S, Zenkel M, Mardin CY, Weisschuh N, et al. Journal article