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A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatment.
Maclean KN, Sikora J, Kožich V, Jiang H, Greiner LS, Kraus E, Krijt J, Overdier KH, Collard R, Brodsky GL, Meltesen L, Crnic LS, Allen RH, Stabler SP, Elleder M, Rozen R, Patterson D, Kraus JP. Maclean KN, et al. Among authors: brodsky gl. Mol Genet Metab. 2010 Oct-Nov;101(2-3):153-62. doi: 10.1016/j.ymgme.2010.06.010. Epub 2010 Jun 23. Mol Genet Metab. 2010. PMID: 20638879 Free PMC article.
Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice.
Tomberg K, Khoriaty R, Westrick RJ, Fairfield HE, Reinholdt LG, Brodsky GL, Davizon-Castillo P, Ginsburg D, Di Paola J. Tomberg K, et al. Among authors: brodsky gl. PLoS One. 2016 Mar 7;11(3):e0150852. doi: 10.1371/journal.pone.0150852. eCollection 2016. PLoS One. 2016. PMID: 26950939 Free PMC article.
Localization of STCH to human chromosome 21q11.1.
Brodsky G, Otterson GA, Parry BB, Hart I, Patterson D, Kaye FJ. Brodsky G, et al. Genomics. 1995 Dec 10;30(3):627-8. doi: 10.1006/geno.1995.1291. Genomics. 1995. PMID: 8825657 No abstract available.
31 results