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Julia Haupt
Julia Haupt
University of Pennsylvania
Biology
Fibrodysplasia ossificans progressiva
ACVR1
Mutation
Genetics
4
Papers
121
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ACVR1R206H FOP mutation alters mechanosensing and tissue stiffness during heterotopic ossification
2019
Molecular Biology of the Cell
Julia Haupt
Alexandra Stanley
Claire M. McLeod
Brian D. Cosgrove
Andria L. Culbert
Linda Wang
Foteini Mourkioti
Robert L. Mauck
Eileen M. Shore
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Citations (19)
Variable signaling activity by FOP ACVR1 mutations
2017
Bone
Julia Haupt
Meiqi Xu
Eileen M. Shore
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Citations (24)
TGF-β Family Signaling in Connective Tissue and Skeletal Diseases
2017
Cold Spring Harbor Perspectives in Biology
Elena Gallo MacFarlane
Julia Haupt
Harry C. Dietz
Eileen M. Shore
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Citations (42)
ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variant
2014
Human Molecular Genetics
Julia Haupt
Alexandra Deichsel
Katja Stange
Cindy Ast
Renata Bocciardi
Roberto Ravazzolo
Maja Di Rocco
Paola Ferrari
Antonio Landi
Frederick S. Kaplan
Eileen M. Shore
Carsten Reissner
Petra Seemann
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Citations (36)
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