Braunstein EM - Search Results

1

A germline ERBB3 variant is a candidate for predisposition to erythroid MDS/erythroleukemia.

Braunstein EM, Li R, Sobreira N, Marosy B, Hetrick K, Doheny K, Gocke CD, Valle D, Brodsky RA, Cheng L. Braunstein EM, et al. Leukemia. 2016 Nov;30(11):2242-2245. doi: 10.1038/leu.2016.173. Epub 2016 Jun 15. Leukemia. 2016. PMID: 27416908 Free PMC article. No abstract available.

2

Generation of glycosylphosphatidylinositol anchor protein-deficient blood cells from human induced pluripotent stem cells.

Yuan X, Braunstein EM, Ye Z, Liu CF, Chen G, Zou J, Cheng L, Brodsky RA. Yuan X, et al. Among authors: braunstein em. Stem Cells Transl Med. 2013 Nov;2(11):819-29. doi: 10.5966/sctm.2013-0069. Epub 2013 Oct 10. Stem Cells Transl Med. 2013. PMID: 24113066 Free PMC article.

3

Efficient and allele-specific genome editing of disease loci in human iPSCs.

Smith C, Abalde-Atristain L, He C, Brodsky BR, Braunstein EM, Chaudhari P, Jang YY, Cheng L, Ye Z. Smith C, et al. Among authors: braunstein em. Mol Ther. 2015 Mar;23(3):570-7. doi: 10.1038/mt.2014.226. Epub 2014 Nov 24. Mol Ther. 2015. PMID: 25418680 Free PMC article.

4

Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia.

Li R, Sobreira N, Witmer PD, Pratz KW, Braunstein EM. Li R, et al. Among authors: braunstein em. Haematologica. 2016 Jun;101(6):e228-31. doi: 10.3324/haematol.2015.139790. Epub 2016 Mar 4. Haematologica. 2016. PMID: 26944477 Free PMC article. No abstract available.

5

A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model.

Yuan X, Li Z, Baines AC, Gavriilaki E, Ye Z, Wen Z, Braunstein EM, Biesecker LG, Cheng L, Dong X, Brodsky RA. Yuan X, et al. Among authors: braunstein em. PLoS One. 2017 Apr 25;12(4):e0174074. doi: 10.1371/journal.pone.0174074. eCollection 2017. PLoS One. 2017. PMID: 28441409 Free PMC article.

6

Germline mutations in the alternative pathway of complement predispose to HELLP syndrome.

Vaught AJ, Braunstein EM, Jasem J, Yuan X, Makhlin I, Eloundou S, Baines AC, Merrill SA, Chaturvedi S, Blakemore K, Sperati CJ, Brodsky RA. Vaught AJ, et al. Among authors: braunstein em. JCI Insight. 2018 Mar 22;3(6):e99128. doi: 10.1172/jci.insight.99128. JCI Insight. 2018. PMID: 29563339 Free PMC article.

7

A prospective quality improvement initiative in adult hemophagocytic lymphohistiocytosis to improve testing and a framework to facilitate trigger identification and mitigate hemorrhage from retrospective analysis.

Merrill SA, Naik R, Streiff MB, Shanbhag S, Lanzkron S, Braunstein EM, Moliterno AM, Brodsky RA. Merrill SA, et al. Among authors: braunstein em. Medicine (Baltimore). 2018 Aug;97(31):e11579. doi: 10.1097/MD.0000000000011579. Medicine (Baltimore). 2018. PMID: 30075527 Free PMC article.

8

Reduced ADAMTS13 activity during TTP remission is associated with stroke in TTP survivors.

Upreti H, Kasmani J, Dane K, Braunstein EM, Streiff MB, Shanbhag S, Moliterno AR, Sperati CJ, Gottesman RF, Brodsky RA, Kickler TS, Chaturvedi S. Upreti H, et al. Among authors: braunstein em. Blood. 2019 Sep 26;134(13):1037-1045. doi: 10.1182/blood.2019001056. Epub 2019 Aug 20. Blood. 2019. PMID: 31431443 Free PMC article.

9

Complement activity and complement regulatory gene mutations are associated with thrombosis in APS and CAPS.

Chaturvedi S, Braunstein EM, Yuan X, Yu J, Alexander A, Chen H, Gavriilaki E, Alluri R, Streiff MB, Petri M, Crowther MA, McCrae KR, Brodsky RA. Chaturvedi S, et al. Among authors: braunstein em. Blood. 2020 Jan 23;135(4):239-251. doi: 10.1182/blood.2019003863. Blood. 2020. PMID: 31812994 Free PMC article.

10

A review of the alternative pathway of complement and its relation to HELLP syndrome: is it time to consider HELLP syndrome a disease of the alternative pathway.

Vaught AJ, Braunstein E, Chaturvedi S, Blakemore K, Brodsky RA. Vaught AJ, et al. J Matern Fetal Neonatal Med. 2022 Apr;35(7):1392-1400. doi: 10.1080/14767058.2020.1755650. Epub 2020 Apr 26. J Matern Fetal Neonatal Med. 2022. PMID: 32338085 Review.

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