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Report of a young girl with MYH9 mutation and review of the literature.
Landi D, Lockhart E, Miller SE, Datto M, Rehder C, Kanaly A, Thornburg CD. Landi D, et al. Among authors: miller se. J Pediatr Hematol Oncol. 2012 Oct;34(7):538-40. doi: 10.1097/MPH.0b013e3182678fc9. J Pediatr Hematol Oncol. 2012. PMID: 23007341 Review.
Deletion of the protein kinase A/protein kinase G target SMTNL1 promotes an exercise-adapted phenotype in vascular smooth muscle.
Wooldridge AA, Fortner CN, Lontay B, Akimoto T, Neppl RL, Facemire C, Datto MB, Kwon A, McCook E, Li P, Wang S, Thresher RJ, Miller SE, Perriard JC, Gavin TP, Hickner RC, Coffman TM, Somlyo AV, Yan Z, Haystead TA. Wooldridge AA, et al. Among authors: miller se. J Biol Chem. 2008 Apr 25;283(17):11850-9. doi: 10.1074/jbc.M708628200. Epub 2008 Feb 29. J Biol Chem. 2008. PMID: 18310078 Free PMC article.
TNXB mutations can cause vesicoureteral reflux.
Gbadegesin RA, Brophy PD, Adeyemo A, Hall G, Gupta IR, Hains D, Bartkowiak B, Rabinovich CE, Chandrasekharappa S, Homstad A, Westreich K, Wu G, Liu Y, Holanda D, Clarke J, Lavin P, Selim A, Miller S, Wiener JS, Ross SS, Foreman J, Rotimi C, Winn MP. Gbadegesin RA, et al. J Am Soc Nephrol. 2013 Jul;24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25. J Am Soc Nephrol. 2013. PMID: 23620400 Free PMC article.
Visualization of SARS-CoV-2 in the Lung.
Miller SE. Miller SE. N Engl J Med. 2020 Dec 31;383(27):2689. doi: 10.1056/NEJMc2030450. N Engl J Med. 2020. PMID: 33394576 No abstract available.
392 results