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Genetic Analysis of Japanese Children Clinically Diagnosed with Familial Hypercholesterolemia.
Nagahara K, Nishibukuro T, Ogiwara Y, Ikegawa K, Tada H, Yamagishi M, Kawashiri MA, Ochi A, Toyoda J, Nakano Y, Adachi M, Mizuno K, Hasegawa Y, Dobashi K. Nagahara K, et al. Among authors: yamagishi m. J Atheroscler Thromb. 2022 May 1;29(5):667-677. doi: 10.5551/jat.62807. Epub 2021 May 20. J Atheroscler Thromb. 2022. PMID: 34011801 Free PMC article.
High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.
Nohara A, Kawashiri MA, Claudel T, Mizuno M, Tsuchida M, Takata M, Katsuda S, Miwa K, Inazu A, Kuipers F, Kobayashi J, Koizumi J, Yamagishi M, Mabuchi H. Nohara A, et al. Among authors: yamagishi m. Arterioscler Thromb Vasc Biol. 2007 Apr;27(4):923-8. doi: 10.1161/01.ATV.0000258945.76141.8a. Epub 2007 Feb 1. Arterioscler Thromb Vasc Biol. 2007. PMID: 17272748
[Molecular mechanism of reverse cholesterol transport].
Kawashiri MA, Yamagishi M, Kobayashi J, Mabuchi H, Inazu A. Kawashiri MA, et al. Among authors: yamagishi m. Nihon Rinsho. 2007 Jul 28;65 Suppl 7:47-52. Nihon Rinsho. 2007. PMID: 17824012 Review. Japanese. No abstract available.
Apolipoprotein B gene mutations and fatty liver in Japanese hypobetalipoproteinemia.
Katsuda S, Kawashiri MA, Inazu A, Tada H, Tsuchida M, Kaneko Y, Nozue T, Nohara A, Okada T, Kobayashi J, Michishita I, Mabuchi H, Yamagishi M. Katsuda S, et al. Among authors: yamagishi m. Clin Chim Acta. 2009 Jan;399(1-2):64-8. doi: 10.1016/j.cca.2008.09.021. Epub 2008 Sep 24. Clin Chim Acta. 2009. PMID: 18848826
1,298 results