Publications by authors named "Nele Vollersen"

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The WNT1 mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV.
Nele Vollersen, Wenbo Zhao, Tim Rolvien, Fabiola Lange, Felix Nikolai Schmidt

Bone Res· November 2021

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Mice Carrying a Ubiquitous R235W Mutation of Wnt1 Display a Bone-Specific Phenotype.
Timur Alexander Yorgan, Tim Rolvien, Julian Stürznickel, Nele Vollersen, Fabiola Lange

J Bone Miner Res· September 2020

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Wnt1 is an Lrp5-independent bone-anabolic Wnt ligand.
Julia Luther, Timur Alexander Yorgan, Tim Rolvien, Lorenz Ulsamer, Till Koehne, Nele Vollersen

Sci Transl Med· November 2018

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High Bone Turnover in Mice Carrying a Pathogenic Notch2 Mutation Causing Hajdu-Cheney Syndrome.
Nele Vollersen, Irm Hermans-Borgmeyer, Kerstin Cornils, Boris Fehse, Tim Rolvien

J Bone Miner Res· January 2018

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Osteoblast-specific Notch2 inactivation causes increased trabecular bone mass at specific sites of the appendicular skeleton.
Timur Yorgan, Nele Vollersen, Christoph Riedel, Anke Jeschke, Stephanie Peters

Bone· June 2016

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