Haupt J - Search Results

1

The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralization.

Shen Q, Little SC, Xu M, Haupt J, Ast C, Katagiri T, Mundlos S, Seemann P, Kaplan FS, Mullins MC, Shore EM. Shen Q, et al. Among authors: haupt j. J Clin Invest. 2009 Nov;119(11):3462-72. doi: 10.1172/JCI37412. Epub 2009 Oct 12. J Clin Invest. 2009. PMID: 19855136 Free PMC article.

2

ACVR1 p.Q207E causes classic fibrodysplasia ossificans progressiva and is functionally distinct from the engineered constitutively active ACVR1 p.Q207D variant.

Haupt J, Deichsel A, Stange K, Ast C, Bocciardi R, Ravazzolo R, Di Rocco M, Ferrari P, Landi A, Kaplan FS, Shore EM, Reissner C, Seemann P. Haupt J, et al. Hum Mol Genet. 2014 Oct 15;23(20):5364-77. doi: 10.1093/hmg/ddu255. Epub 2014 May 22. Hum Mol Genet. 2014. PMID: 24852373 Free PMC article.

3

Variable signaling activity by FOP ACVR1 mutations.

Haupt J, Xu M, Shore EM. Haupt J, et al. Bone. 2018 Apr;109:232-240. doi: 10.1016/j.bone.2017.10.027. Epub 2017 Oct 31. Bone. 2018. PMID: 29097342 Free PMC article.

4

Investigations of activated ACVR1/ALK2, a bone morphogenetic protein type I receptor, that causes fibrodysplasia ossificans progressiva.

Kaplan FS, Seemann P, Haupt J, Xu M, Lounev VY, Mullins M, Shore EM. Kaplan FS, et al. Among authors: haupt j. Methods Enzymol. 2010;484:357-73. doi: 10.1016/B978-0-12-381298-8.00018-6. Methods Enzymol. 2010. PMID: 21036241 Free PMC article.

5

ACVR1^R206H FOP mutation alters mechanosensing and tissue stiffness during heterotopic ossification.

Haupt J, Stanley A, McLeod CM, Cosgrove BD, Culbert AL, Wang L, Mourkioti F, Mauck RL, Shore EM. Haupt J, et al. Mol Biol Cell. 2019 Jan 1;30(1):17-29. doi: 10.1091/mbc.E18-05-0311. Epub 2018 Oct 31. Mol Biol Cell. 2019. PMID: 30379592 Free PMC article.

6

TGF-β Family Signaling in Connective Tissue and Skeletal Diseases.

MacFarlane EG, Haupt J, Dietz HC, Shore EM. MacFarlane EG, et al. Among authors: haupt j. Cold Spring Harb Perspect Biol. 2017 Nov 1;9(11):a022269. doi: 10.1101/cshperspect.a022269. Cold Spring Harb Perspect Biol. 2017. PMID: 28246187 Free PMC article. Review.

7

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

Villavicencio-Lorini P, Kuss P, Friedrich J, Haupt J, Farooq M, Türkmen S, Duboule D, Hecht J, Mundlos S. Villavicencio-Lorini P, et al. Among authors: haupt j. J Clin Invest. 2010 Jun;120(6):1994-2004. doi: 10.1172/JCI41554. Epub 2010 May 10. J Clin Invest. 2010. PMID: 20458143 Free PMC article.

8

Stricker S, Mathia S, Haupt J, Seemann P, Meier J, Mundlos S. Stricker S, et al. Among authors: haupt j. Stem Cells Dev. 2012 Mar 1;21(4):623-33. doi: 10.1089/scd.2011.0154. Epub 2011 Jul 26. Stem Cells Dev. 2012. PMID: 21671783

9

Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN.

Seemann P, Brehm A, König J, Reissner C, Stricker S, Kuss P, Haupt J, Renninger S, Nickel J, Sebald W, Groppe JC, Plöger F, Pohl J, Schmidt-von Kegler M, Walther M, Gassner I, Rusu C, Janecke AR, Dathe K, Mundlos S. Seemann P, et al. Among authors: haupt j. PLoS Genet. 2009 Nov;5(11):e1000747. doi: 10.1371/journal.pgen.1000747. Epub 2009 Nov 26. PLoS Genet. 2009. PMID: 19956691 Free PMC article.

10

Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development.

Stricker S, Brieske N, Haupt J, Mundlos S. Stricker S, et al. Among authors: haupt j. Gene Expr Patterns. 2006 Oct;6(8):826-34. doi: 10.1016/j.modgep.2006.02.003. Epub 2006 Mar 22. Gene Expr Patterns. 2006. PMID: 16554187

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