Mabuchi H - Search Results

1

Novel mutations of cholesteryl ester transfer protein (CETP) gene in Japanese hyperalphalipoproteinemic subjects.

Ohtani R, Inazu A, Noji Y, Wakasugi T, Miwa K, Tada H, Kawashiri MA, Noguchi T, Nohara A, Kobayashi J, Koizumi J, Yamagishi M, Mabuchi H. Ohtani R, et al. Among authors: mabuchi h. Clin Chim Acta. 2012 Mar 22;413(5-6):537-43. doi: 10.1016/j.cca.2011.11.010. Epub 2011 Nov 19. Clin Chim Acta. 2012. PMID: 22122993 Free article.

2

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: mabuchi h. 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

3

A novel method for determining functional LDL receptor activity in familial hypercholesterolemia: application of the CD3/CD28 assay in lymphocytes.

Tada H, Kawashiri MA, Noguchi T, Mori M, Tsuchida M, Takata M, Nohara A, Inazu A, Kobayashi J, Yachie A, Mabuchi H, Yamagishi M. Tada H, et al. Among authors: mabuchi h. Clin Chim Acta. 2009 Feb;400(1-2):42-7. doi: 10.1016/j.cca.2008.10.010. Epub 2008 Oct 26. Clin Chim Acta. 2009. PMID: 19013141

4

Cholesterol efflux from J774 macrophages and Fu5AH hepatoma cells to serum is preserved in CETP-deficient patients.

Miwa K, Inazu A, Kawashiri M, Nohara A, Higashikata T, Kobayashi J, Koizumi J, Nakajima K, Nakano T, Niimi M, Mabuchi H, Yamagishi M. Miwa K, et al. Among authors: mabuchi h. Clin Chim Acta. 2009 Apr;402(1-2):19-24. doi: 10.1016/j.cca.2008.12.012. Epub 2008 Dec 14. Clin Chim Acta. 2009. PMID: 19135042

5

Impact of bezafibrate and atorvastatin on lipoprotein subclass in patients with type III hyperlipoproteinemia: result from a crossover study.

Kawashiri MA, Kobayashi J, Nohara A, Noguchi T, Tada H, Nakanishi C, Inazu A, Mabuchi H, Yamagishi M. Kawashiri MA, et al. Among authors: mabuchi h. Clin Chim Acta. 2011 May 12;412(11-12):1068-75. doi: 10.1016/j.cca.2011.02.026. Epub 2011 Feb 24. Clin Chim Acta. 2011. PMID: 21354122 Clinical Trial.

6

A novel type of familial hypercholesterolemia: double heterozygous mutations in LDL receptor and LDL receptor adaptor protein 1 gene.

Tada H, Kawashiri MA, Ohtani R, Noguchi T, Nakanishi C, Konno T, Hayashi K, Nohara A, Inazu A, Kobayashi J, Mabuchi H, Yamagishi M. Tada H, et al. Among authors: mabuchi h. Atherosclerosis. 2011 Dec;219(2):663-6. doi: 10.1016/j.atherosclerosis.2011.08.004. Epub 2011 Aug 10. Atherosclerosis. 2011. PMID: 21872251

7

Cholesteryl ester transfer protein (CETP) deficiency and CETP inhibitors.

Mabuchi H, Nohara A, Inazu A. Mabuchi H, et al. Mol Cells. 2014 Nov;37(11):777-84. doi: 10.14348/molcells.2014.0265. Epub 2014 Nov 6. Mol Cells. 2014. PMID: 25410905 Free PMC article. Review.

8

A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing.

Tada H, Hosomichi K, Okada H, Kawashiri MA, Nohara A, Inazu A, Tomizawa S, Tajima A, Mabuchi H, Hayashi K. Tada H, et al. Among authors: mabuchi h. Clin Chim Acta. 2016 Jan 30;453:194-6. doi: 10.1016/j.cca.2015.12.028. Epub 2015 Dec 23. Clin Chim Acta. 2016. PMID: 26721317

9

Clinical whole exome sequencing in severe hypertriglyceridemia.

Tada H, Nomura A, Okada H, Nakahashi T, Nozue T, Hayashi K, Nohara A, Yagi K, Inazu A, Michishita I, Mabuchi H, Yamagishi M, Kawashiri MA. Tada H, et al. Among authors: mabuchi h. Clin Chim Acta. 2019 Jan;488:31-39. doi: 10.1016/j.cca.2018.10.041. Epub 2018 Oct 30. Clin Chim Acta. 2019. PMID: 30389453

10

Dual effects on HDL metabolism by cholesteryl ester transfer protein inhibition in HepG2 cells.

Huang Z, Inazu A, Kawashiri MA, Nohara A, Higashikata T, Mabuchi H. Huang Z, et al. Among authors: mabuchi h. Am J Physiol Endocrinol Metab. 2003 Jun;284(6):E1210-9. doi: 10.1152/ajpendo.00453.2002. Epub 2003 Feb 25. Am J Physiol Endocrinol Metab. 2003. PMID: 12604506 Free article.

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