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In vivo hematopoietic stem cell modification by mRNA delivery.
Science. 2023 Jul 28;381(6656):436-443. doi: 10.1126/science.ade6967. Epub 2023 Jul 27.
Science. 2023.
PMID: 37499029
Combined use of emapalumab and ruxolitinib in a patient with refractory hemophagocytic lymphohistiocytosis was safe and effective.
Triebwasser MP, Barrett DM, Bassiri H, Bunin N, Elgarten C, Freedman J, Geera AS, Monos D, Lambert MP, Olson T, Seif AE, Paessler M, Petrosa W, Reilly AF, Romberg N, Sullivan KE, Quinn GZ, Behrens E, Teachey DT.
Triebwasser MP, et al.
Pediatr Blood Cancer. 2021 Jul;68(7):e29026. doi: 10.1002/pbc.29026. Epub 2021 Mar 22.
Pediatr Blood Cancer. 2021.
PMID: 33754483
Free PMC article.
No abstract available.
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Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulation.
Shahin T, Mayr D, Shoeb MR, Kuehn HS, Hoeger B, Giuliani S, Gawriyski LM, Petronczki ÖY, Hadjadj J, Bal SK, Zoghi S, Haimel M, Jimenez Heredia R, Boutboul D, Triebwasser MP, Rialland-Battisti F, Costedoat Chalumeau N, Quartier P, Tangye SG, Fleisher TA, Rezaei N, Romberg N, Latour S, Varjosalo M, Halbritter F, Rieux-Laucat F, Castanon I, Rosenzweig SD, Boztug K.
Shahin T, et al. Among authors: triebwasser mp.
Blood Adv. 2022 Apr 12;6(7):2444-2451. doi: 10.1182/bloodadvances.2021006367.
Blood Adv. 2022.
PMID: 34920454
Free PMC article.
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Timing and mechanism of conceptus demise in a complement regulatory membrane protein deficient mouse.
Triebwasser MP, Wu X, Bertram P, Hourcade DE, Nelson DM, Atkinson JP.
Triebwasser MP, et al.
Am J Reprod Immunol. 2018 Oct;80(4):e12997. doi: 10.1111/aji.12997. Epub 2018 Jun 20.
Am J Reprod Immunol. 2018.
PMID: 29924462
Free PMC article.
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Mapping rare, deleterious mutations in Factor H: Association with early onset, drusen burden, and lower antigenic levels in familial AMD.
Wagner EK, Raychaudhuri S, Villalonga MB, Java A, Triebwasser MP, Daly MJ, Atkinson JP, Seddon JM.
Wagner EK, et al. Among authors: triebwasser mp.
Sci Rep. 2016 Aug 30;6:31531. doi: 10.1038/srep31531.
Sci Rep. 2016.
PMID: 27572114
Free PMC article.
Clinical Trial.
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Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration.
Triebwasser MP, Roberson ED, Yu Y, Schramm EC, Wagner EK, Raychaudhuri S, Seddon JM, Atkinson JP.
Triebwasser MP, et al.
Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6873-8. doi: 10.1167/iovs.15-17432.
Invest Ophthalmol Vis Sci. 2015.
PMID: 26501415
Free PMC article.
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Genetic variants in the complement system predisposing to age-related macular degeneration: a review.
Schramm EC, Clark SJ, Triebwasser MP, Raychaudhuri S, Seddon J, Atkinson JP.
Schramm EC, et al. Among authors: triebwasser mp.
Mol Immunol. 2014 Oct;61(2):118-125. doi: 10.1016/j.molimm.2014.06.032. Epub 2014 Jul 15.
Mol Immunol. 2014.
PMID: 25034031
Free PMC article.
Review.
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Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration.
Yu Y, Triebwasser MP, Wong EK, Schramm EC, Thomas B, Reynolds R, Mardis ER, Atkinson JP, Daly M, Raychaudhuri S, Kavanagh D, Seddon JM.
Yu Y, et al. Among authors: triebwasser mp.
Hum Mol Genet. 2014 Oct 1;23(19):5283-93. doi: 10.1093/hmg/ddu226. Epub 2014 May 20.
Hum Mol Genet. 2014.
PMID: 24847005
Free PMC article.
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