Takeyoshi Murano
Chiba, 2748510, Japan
Last Updated: 09/26/2026
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Found 23 publications
Factor V Leiden Mutation Diagnosed After the Onset of DVT During Pregnancy in a Woman of Half-Japanese, Half-European Descent.
Journal: Internal medicine (Tokyo, Japan)
Published: June 11, 2025
Current Status of Familial LCAT Deficiency in Japan.
Journal: Journal of atherosclerosis and thrombosis
Published: April 19, 2021
Association of Plasma Xanthine Oxidoreductase with Arterial Stiffness in Type 2 Diabetes with Liver Dysfunction.
Journal: The American journal of the medical sciences
Published: September 18, 2020
Lp8 is potentially associated with partial lecithin:cholesterol acyltransferase deficiency in a patient with primary biliary cirrhosis.
Journal: Journal of clinical lipidology
Published: March 13, 2018
Regulation of secretion and enzymatic activity of lipoprotein lipase by C-mannosylation.
Journal: Biochemical and biophysical research communications
Published: March 07, 2017
Severely impaired activity of lipoprotein lipase Arg243His is partially ameliorated by emulsifying phospholipids in in vitro triolein hydrolysis analysis.
Journal: Annals of clinical biochemistry
Published: January 25, 2017
Lipoprotein Lipase Deficiency (R243H) in a Type 2 Diabetes Patient with Multiple Arterial Aneurysms.
Lipoprotein Lipase Deficiency (R243H) in a Type 2 Diabetes Patient with Multiple Arterial Aneurysms.
Journal: Internal medicine (Tokyo, Japan)
Published: May 07, 2016
Circulating soluble form of LR11, a regulator of smooth muscle cell migration, is a novel marker for intima-media thickness of carotid arteries in type 2 diabetes.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 22, 2016
Levels of soluble LR11/SorLA are highly increased in the bile of patients with biliary tract and pancreatic cancers.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: December 15, 2015
Subfraction analysis of circulating lipoproteins in a patient with Tangier disease due to a novel ABCA1 mutation.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: October 27, 2015
Last Updated: 09/26/2026