Dolrudee Jumlongras, Ph.D. - Publications

Affiliations: 
2003 Harvard University, Cambridge, MA, United States 
Area:
Genetics

6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Agarwal S, Loder S, Brownley C, Cholok D, Mangiavini L, Li J, Breuler C, Sung HH, Li S, Ranganathan K, Peterson J, Tompkins R, Herndon D, Xiao W, Jumlongras D, et al. Inhibition of Hif1α prevents both trauma-induced and genetic heterotopic ossification. Proceedings of the National Academy of Sciences of the United States of America. PMID 26721400 DOI: 10.1073/Pnas.1515397113  0.449
2015 Lloyd WR, Agarwal S, Nigwekar SU, Esmonde-White K, Loder S, Fagan S, Goverman J, Olsen BR, Jumlongras D, Morris MD, Levi B. Raman spectroscopy for label-free identification of calciphylaxis. Journal of Biomedical Optics. 20: 80501. PMID 26263412 DOI: 10.1117/1.Jbo.20.8.080501  0.345
2015 Agarwal S, Loder S, Brownley C, Peterson J, Oluwatobi E, Tompkins R, Herndon D, Sung H, Zeng W, Jumlongras D, Olsen B, Cederna PS, Buchman SR, Levi B. Abstract 20: Defining the Role of the Vasculogenic Niche in Trauma-induced Heterotopic Ossification using Novel Imaging and Lineage-tracing Mice. Plastic and Reconstructive Surgery. 135: 24. PMID 25915234 DOI: 10.1097/01.Prs.0000465468.77621.1C  0.413
2012 Jumlongras D, Lachke SA, O'Connell DJ, Aboukhalil A, Li X, Choe SE, Ho JW, Turbe-Doan A, Robertson EA, Olsen BR, Bulyk ML, Amendt BA, Maas RL. An evolutionarily conserved enhancer regulates Bmp4 expression in developing incisor and limb bud. Plos One. 7: e38568. PMID 22701669 DOI: 10.1371/Journal.Pone.0038568  0.431
2004 Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia. Human Genetics. 114: 242-9. PMID 14689302 DOI: 10.1007/S00439-003-1066-6  0.405
2001 Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. A nonsense mutation in MSX1 causes Witkop syndrome. American Journal of Human Genetics. 69: 67-74. PMID 11369996 DOI: 10.1086/321271  0.467
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