Publications by authors named "Ina Prade"

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Biphasic bone substitutes coated with PLGA incorporating therapeutic ions Sr and Mg: cytotoxicity cascade and response of immune and bone regeneration.
Yanru Ren, Ole Jung, Milijana Batinic, Kim Burckhardt, Oliver Görke, Ina Prade

Front Bioeng Biotechnol· June 2024

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Human endothelial cells form an endothelium in freestanding collagen hollow filaments fabricated by direct extrusion printing.
Ina Prade, Michaela Schröpfer, Caroline Seidel, Claudia Krumbiegel, Tina Hille

Biomater Biosyst· December 2022

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Gas-Phase Fluorination on PLA Improves Cell Adhesion and Spreading.
Michaela Schroepfer, Frauke Junghans, Diana Voigt, Michael Meyer, Anette Breier, Ina Prade

ACS Omega· March 2020

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Enhanced Growth of Lapine Anterior Cruciate Ligament-Derived Fibroblasts on Scaffolds Embroidered from Poly(l-lactide--ε-caprolactone) and Polylactic Acid Threads Functionalized by Fluorination and Hexamethylene Diisocyanate Cross-Linked Collagen Foams.
Clemens Gögele, Judith Hahn, Cindy Elschner, Annette Breier, Michaela Schröpfer, Ina Prade

Int J Mol Sci· February 2020

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PHD4 stimulates tumor angiogenesis in osteosarcoma cells via TGF-α.
Anne Klotzsche-von Ameln, Ina Prade, Marianne Grosser, Antje Kettelhake, Maryam Rezaei

Mol Cancer Res· November 2013

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Parameter estimation with a novel gradient-based optimization method for biological lattice-gas cellular automaton models.
Carsten Mente, Ina Prade, Lutz Brusch, Georg Breier, Andreas Deutsch

J Math Biol· July 2011

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A designed cell-permeable aptamer-based corepressor peptide is highly specific for the androgen receptor and inhibits prostate cancer cell growth in a vector-free mode.
Christina A Reeb, Claudia Gerlach, Maria Heinssmann, Ina Prade, Jocelyn Ceraline

Endocrinology· June 2011

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Inhibition of HIF prolyl hydroxylase-2 blocks tumor growth in mice through the antiproliferative activity of TGFβ.
Anne Klotzsche-von Ameln, Antje Muschter, Soulafa Mamlouk, Joanna Kalucka, Ina Prade

Cancer Res· May 2011

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The natural compound atraric acid is an antagonist of the human androgen receptor inhibiting cellular invasiveness and prostate cancer cell growth.
Maria Papaioannou, Sonja Schleich, Ina Prade, Stephanie Degen, Daniela Roell

J Cell Mol Med· August 2009

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Wild-type but not mutant androgen receptor inhibits expression of the hTERT telomerase subunit: a novel role of AR mutation for prostate cancer development.
Udo Moehren, Maria Papaioannou, Christina A Reeb, Annalisa Grasselli, Simona Nanni, Ina Prade

FASEB J· April 2008

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