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Alexandra Deichsel

Showing results (1-10 of 5) with videos related to

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Cell Cycle (Georgetown, Tex.)|January 23, 2009
The ubiquitin-selective chaperone CDC-48/p97, a new player in DNA replicationAlexandra Deichsel, Julien Mouysset, Thorsten Hoppe
Cellular Signalling|November 7, 2016
The Fibrodysplasia Ossificans Progressiva (FOP) mutation p.R206H in ACVR1 confers an altered ligand responseLaura Hildebrand, Katja Stange, Alexandra Deichsel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2008
Cell cycle progression requires the CDC-48UFD-1/NPL-4 complex for efficient DNA replicationJulien Mouysset, Alexandra Deichsel, Sandra Moser, et al.
Human Molecular Genetics|May 24, 2014
ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variantJulia Haupt, Alexandra Deichsel, Katja Stange, et al.
European Journal of Human Genetics : EJHG|October 17, 2013
Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type GrebeLuitgard M Graul-Neumann, Alexandra Deichsel, Ulrike Wille, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Cell Cycle (Georgetown, Tex.)|January 23, 2009
The ubiquitin-selective chaperone CDC-48/p97, a new player in DNA replicationAlexandra Deichsel, Julien Mouysset, Thorsten Hoppe
Cellular Signalling|November 7, 2016
The Fibrodysplasia Ossificans Progressiva (FOP) mutation p.R206H in ACVR1 confers an altered ligand responseLaura Hildebrand, Katja Stange, Alexandra Deichsel, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2008
Cell cycle progression requires the CDC-48UFD-1/NPL-4 complex for efficient DNA replicationJulien Mouysset, Alexandra Deichsel, Sandra Moser, et al.
Human Molecular Genetics|May 24, 2014
ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variantJulia Haupt, Alexandra Deichsel, Katja Stange, et al.
European Journal of Human Genetics : EJHG|October 17, 2013
Homozygous missense and nonsense mutations in BMPR1B cause acromesomelic chondrodysplasia-type GrebeLuitgard M Graul-Neumann, Alexandra Deichsel, Ulrike Wille, et al.
Pageof 1