M
Michaela Kneissel
Researcher at Novartis
Publications - 100
Citations - 8372
Michaela Kneissel is an academic researcher from Novartis. The author has contributed to research in topics: Sclerostin & Osteoblast. The author has an hindex of 41, co-authored 98 publications receiving 7451 citations. Previous affiliations of Michaela Kneissel include University of Vienna.
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Journal ArticleDOI
WNT signaling in bone homeostasis and disease: from human mutations to treatments
Roland Baron,Michaela Kneissel +1 more
TL;DR: Current understanding of the mechanisms by which WNT signalng regulates bone homeostasis is reviewed, finding the pathway is now the target for therapeutic intervention to restore bone strength in millions of patients at risk for fracture.
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SOST is a target gene for PTH in bone.
TL;DR: It is shown that PTH directly inhibits SOST transcription in vivo and in vitro, suggesting that SOST regulation may play a role in mediating PTH action in bone.
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Osteocyte Wnt/β-Catenin Signaling Is Required for Normal Bone Homeostasis
Ina Kramer,Christine Halleux,Hansjoerg Keller,Marco Pegurri,Jonathan H. Gooi,Patricia Brander Weber,Jian Q. Feng,Lynda F. Bonewald,Michaela Kneissel +8 more
TL;DR: Results reveal a crucial novel function for osteocyte β-catenin signaling in controlling bone homeostasis in osteocyte-specific β- catenin mutants.
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Mice Lacking Histone Deacetylase 6 Have Hyperacetylated Tubulin but Are Viable and Develop Normally
Yu Zhang,So Hee Kwon,Teppei Yamaguchi,Fabien Cubizolles,Sophie Rousseaux,Michaela Kneissel,Chun Cao,Na Li,Hwei Ling Cheng,Katrin F. Chua,David B. Lombard,Adam Mizeracki,Gabriele Matthias,Frederick W. Alt,Saadi Khochbin,Patrick Matthias +15 more
TL;DR: It is demonstrated that mice survive well without HDAC6 and that tubulin hyperacetylation is not detrimental to normal mammalian development, and that this deacetylase plays a minor role in bone biology.
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Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease
Gabriela G. Loots,Michaela Kneissel,Hansjoerg Keller,Myma Baptist,Jessie Chang,Nicole M. Collette,Dmitriy Ovcharenko,Ingrid Plajzer-Frick,Edward M. Rubin +8 more
TL;DR: A comparative sequence-based approach to characterize a large noncoding region deleted in patients affected by Van Buchem (VB) disease, a severe sclerosing bone dysplasia, and identifies a candidate enhancer element that drives human SOST expression in osteoblast-like cell lines in vitro and in the skeletal anlage of the embryonic day 14.5 mouse embryo.