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Page 1
[Fibrinogen genes polymorphism in patients with ischemic stroke].
Gusev EI, Favorova OO, Sudomoina MA, Martynov MIu, Serdiuk IE, Parfenov MG, Nikonova AA. Gusev EI, et al. Among authors: parfenov mg. Zh Nevrol Psikhiatr Im S S Korsakova. 2008;108(4):91-8. Zh Nevrol Psikhiatr Im S S Korsakova. 2008. PMID: 18567199 Review. Russian. No abstract available.
Prevention of experimental autoimmune encephalomyelitis in DA rats by grafting primary skin fibroblasts engineered to express transforming growth factor-beta1.
Zargarova T, Kulakova O, Prassolov V, Zharmukhamedova T, Tsyganova V, Turobov V, Ivanov D, Parfenov M, Sudomoina M, Chernajovsky Y, Favorova O. Zargarova T, et al. Clin Exp Immunol. 2004 Aug;137(2):313-9. doi: 10.1111/j.1365-2249.2004.02539.x. Clin Exp Immunol. 2004. PMID: 15270848 Free PMC article.
Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice.
Domenighetti AA, Chu PH, Wu T, Sheikh F, Gokhin DS, Guo LT, Cui Z, Peter AK, Christodoulou DC, Parfenov MG, Gorham JM, Li DY, Banerjee I, Lai X, Witzmann FA, Seidman CE, Seidman JG, Gomes AV, Shelton GD, Lieber RL, Chen J. Domenighetti AA, et al. Among authors: parfenov mg. Hum Mol Genet. 2014 Jan 1;23(1):209-25. doi: 10.1093/hmg/ddt412. Epub 2013 Aug 23. Hum Mol Genet. 2014. PMID: 23975679 Free PMC article.
Molecular profiling of dilated cardiomyopathy that progresses to heart failure.
Burke MA, Chang S, Wakimoto H, Gorham JM, Conner DA, Christodoulou DC, Parfenov MG, DePalma SR, Eminaga S, Konno T, Seidman JG, Seidman CE. Burke MA, et al. Among authors: parfenov mg. JCI Insight. 2016 May 5;1(6):e86898. doi: 10.1172/jci.insight.86898. JCI Insight. 2016. PMID: 27239561 Free PMC article.
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.
Manheimer KB, Patel N, Richter F, Gorham J, Tai AC, Homsy J, Boskovski MT, Parfenov M, Goldmuntz E, Chung WK, Brueckner M, Tristani-Firouzi M, Srivastava D, Seidman JG, Seidman CE, Gelb BD, Sharp AJ. Manheimer KB, et al. Hum Mutat. 2018 Jun;39(6):870-881. doi: 10.1002/humu.23419. Epub 2018 Mar 22. Hum Mutat. 2018. PMID: 29527824 Free PMC article.
Genomic analyses implicate noncoding de novo variants in congenital heart disease.
Richter F, Morton SU, Kim SW, Kitaygorodsky A, Wasson LK, Chen KM, Zhou J, Qi H, Patel N, DePalma SR, Parfenov M, Homsy J, Gorham JM, Manheimer KB, Velinder M, Farrell A, Marth G, Schadt EE, Kaltman JR, Newburger JW, Giardini A, Goldmuntz E, Brueckner M, Kim R, Porter GA Jr, Bernstein D, Chung WK, Srivastava D, Tristani-Firouzi M, Troyanskaya OG, Dickel DE, Shen Y, Seidman JG, Seidman CE, Gelb BD. Richter F, et al. Nat Genet. 2020 Aug;52(8):769-777. doi: 10.1038/s41588-020-0652-z. Epub 2020 Jun 29. Nat Genet. 2020. PMID: 32601476 Free PMC article. Clinical Trial.
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