Publications by authors named "Alexandra Deichsel"

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The Fibrodysplasia Ossificans Progressiva (FOP) mutation p.R206H in ACVR1 confers an altered ligand response.
Laura Hildebrand, Katja Stange, Alexandra Deichsel, Manfred Gossen, Petra Seemann

Cell Signal· January 2017

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ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variant.
Julia Haupt, Alexandra Deichsel, Katja Stange, Cindy Ast, Renata Bocciardi

Hum Mol Genet· October 2014

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Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type Grebe.
Luitgard M Graul-Neumann, Alexandra Deichsel, Ulrike Wille, Naseebullah Kakar, Randi Koll

Eur J Hum Genet· June 2014

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The ubiquitin-selective chaperone CDC-48/p97, a new player in DNA replication.
Alexandra Deichsel, Julien Mouysset, Thorsten Hoppe

Cell Cycle· January 2009

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Cell cycle progression requires the CDC-48UFD-1/NPL-4 complex for efficient DNA replication.
Julien Mouysset, Alexandra Deichsel, Sandra Moser, Carsten Hoege, Anthony A Hyman

Proc Natl Acad Sci U S A· September 2008

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