Triffitt JT - Search Results

1

Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.

Petrie KA, Lee WH, Bullock AN, Pointon JJ, Smith R, Russell RG, Brown MA, Wordsworth BP, Triffitt JT. Petrie KA, et al. Among authors: triffitt jt. PLoS One. 2009;4(3):e5005. doi: 10.1371/journal.pone.0005005. Epub 2009 Mar 30. PLoS One. 2009. PMID: 19330033 Free PMC article.

2

A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date.

Gregson CL, Hollingworth P, Williams M, Petrie KA, Bullock AN, Brown MA, Tobias JH, Triffitt JT. Gregson CL, et al. Among authors: triffitt jt. Bone. 2011 Mar 1;48(3):654-8. doi: 10.1016/j.bone.2010.10.164. Epub 2010 Oct 29. Bone. 2011. PMID: 21044902 Free PMC article.

3

Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva.

Chaikuad A, Alfano I, Kerr G, Sanvitale CE, Boergermann JH, Triffitt JT, von Delft F, Knapp S, Knaus P, Bullock AN. Chaikuad A, et al. Among authors: triffitt jt. J Biol Chem. 2012 Oct 26;287(44):36990-8. doi: 10.1074/jbc.M112.365932. Epub 2012 Sep 12. J Biol Chem. 2012. PMID: 22977237 Free PMC article.

4

A new class of small molecule inhibitor of BMP signaling.

Sanvitale CE, Kerr G, Chaikuad A, Ramel MC, Mohedas AH, Reichert S, Wang Y, Triffitt JT, Cuny GD, Yu PB, Hill CS, Bullock AN. Sanvitale CE, et al. Among authors: triffitt jt. PLoS One. 2013 Apr 30;8(4):e62721. doi: 10.1371/journal.pone.0062721. Print 2013. PLoS One. 2013. PMID: 23646137 Free PMC article.

5

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.

Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho TJ, Choi IH, Connor JM, Delai P, Glaser DL, LeMerrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS. Shore EM, et al. Among authors: triffitt jt. Nat Genet. 2006 May;38(5):525-7. doi: 10.1038/ng1783. Epub 2006 Apr 23. Nat Genet. 2006. PMID: 16642017

6

Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva.

Virdi AS, Shore EM, Oreffo RO, Li M, Connor JM, Smith R, Kaplan FS, Triffitt JT. Virdi AS, et al. Among authors: triffitt jt. Calcif Tissue Int. 1999 Sep;65(3):250-5. doi: 10.1007/s002239900693. Calcif Tissue Int. 1999. PMID: 10441661

7

Bones in muscles: the problems of soft tissue ossification.

Smith R, Triffitt JT. Smith R, et al. Among authors: triffitt jt. Q J Med. 1986 Nov;61(235):985-90. Q J Med. 1986. PMID: 3116592 Review. No abstract available.

8

From nuclear physics to bone cell biology--Maureen Owen--1927-2011.

Triffitt JT, Russell RG. Triffitt JT, et al. Bone. 2011 Dec;49(6):1121-4. doi: 10.1016/j.bone.2011.10.015. Bone. 2011. PMID: 22206099 No abstract available.

9

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

Feldman G, Li M, Martin S, Urbanek M, Urtizberea JA, Fardeau M, LeMerrer M, Connor JM, Triffitt J, Smith R, Muenke M, Kaplan FS, Shore EM. Feldman G, et al. Am J Hum Genet. 2000 Jan;66(1):128-35. doi: 10.1086/302724. Am J Hum Genet. 2000. PMID: 10631143 Free PMC article.

10

Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP).

Xu MQ, Feldman G, Le Merrer M, Shugart YY, Glaser DL, Urtizberea JA, Fardeau M, Connor JM, Triffitt J, Smith R, Shore EM, Kaplan FS. Xu MQ, et al. Clin Genet. 2000 Oct;58(4):291-8. doi: 10.1034/j.1399-0004.2000.580407.x. Clin Genet. 2000. PMID: 11076054

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