Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Akihiro Inazu

Showing results (41-50 of 87) with videos related to

Pageof 9
Sort By:
Clinical Science (London, England : 1979)|July 11, 2006
CETP (cholesteryl ester transfer protein) promoter -1337 C>T polymorphism protects against coronary atherosclerosis in Japanese patients with heterozygous familial hypercholesterolaemiaMutsuko Takata, Akihiro Inazu, Shoji Katsuda, et al.
The American Journal of Cardiology|September 27, 2017
Assessments of Carotid Artery Plaque Burden in Patients With Familial HypercholesterolemiaHayato Tada, Masa-Aki Kawashiri, Hirofumi Okada, et al.
Journal of Lipid and Atherosclerosis|February 1, 2024
Putative Pathogenic Variants of <i>ABCG5</i> and <i>ABCG8</i> of Sitosterolemia in Patients With Hyper-Low-Density Lipoprotein CholesterolemiaNobuko Kojima, Hayato Tada, Akihiro Nomura, et al.
Journal of Atherosclerosis and Thrombosis|December 6, 2006
The relationship of percent body fat by bioelectrical impedance analysis with blood pressure, and glucose and lipid parametersJunji Kobayashi, Shunichi Murano, Isao Kawamura, et al.
Journal of Clinical Lipidology|September 23, 2018
Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery diseaseHayato Tada, Masa-Aki Kawashiri, Akihiro Nomura, et al.
Atherosclerosis|November 21, 2017
Molecular and functional characterization of familial chylomicronemia syndromeRyota Teramoto, Hayato Tada, Masa-Aki Kawashiri, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 2, 2016
A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencingHayato Tada, Kazuyoshi Hosomichi, Hirofumi Okada, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 4, 2015
Lipoprotein(a) in Familial Hypercholesterolemia With Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function MutationsHayato Tada, Masa-Aki Kawashiri, Taiji Yoshida, et al.
Journal of Lipid Research|December 6, 2003
Apolipoprotein composition of HDL in cholesteryl ester transfer protein deficiencyBela F Asztalos, Katalin V Horvath, Kouji Kajinami, et al.
Internal Medicine (Tokyo, Japan)|January 14, 2005
Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)Yoshihiro Noji, Akihiro Inazu, Toshinori Higashikata, et al.
Pageof 9

Showing results (41-50 of 87) with videos related to

Sort By:
Pageof 9
Clinical Science (London, England : 1979)|July 11, 2006
CETP (cholesteryl ester transfer protein) promoter -1337 C>T polymorphism protects against coronary atherosclerosis in Japanese patients with heterozygous familial hypercholesterolaemiaMutsuko Takata, Akihiro Inazu, Shoji Katsuda, et al.
The American Journal of Cardiology|September 27, 2017
Assessments of Carotid Artery Plaque Burden in Patients With Familial HypercholesterolemiaHayato Tada, Masa-Aki Kawashiri, Hirofumi Okada, et al.
Journal of Lipid and Atherosclerosis|February 1, 2024
Putative Pathogenic Variants of <i>ABCG5</i> and <i>ABCG8</i> of Sitosterolemia in Patients With Hyper-Low-Density Lipoprotein CholesterolemiaNobuko Kojima, Hayato Tada, Akihiro Nomura, et al.
Journal of Atherosclerosis and Thrombosis|December 6, 2006
The relationship of percent body fat by bioelectrical impedance analysis with blood pressure, and glucose and lipid parametersJunji Kobayashi, Shunichi Murano, Isao Kawamura, et al.
Journal of Clinical Lipidology|September 23, 2018
Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery diseaseHayato Tada, Masa-Aki Kawashiri, Akihiro Nomura, et al.
Atherosclerosis|November 21, 2017
Molecular and functional characterization of familial chylomicronemia syndromeRyota Teramoto, Hayato Tada, Masa-Aki Kawashiri, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 2, 2016
A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencingHayato Tada, Kazuyoshi Hosomichi, Hirofumi Okada, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 4, 2015
Lipoprotein(a) in Familial Hypercholesterolemia With Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function MutationsHayato Tada, Masa-Aki Kawashiri, Taiji Yoshida, et al.
Journal of Lipid Research|December 6, 2003
Apolipoprotein composition of HDL in cholesteryl ester transfer protein deficiencyBela F Asztalos, Katalin V Horvath, Kouji Kajinami, et al.
Internal Medicine (Tokyo, Japan)|January 14, 2005
Identification of two novel missense mutations (p.R1221C and p.R1357W) in the ABCC6 (MRP6) gene in a Japanese patient with pseudoxanthoma elasticum (PXE)Yoshihiro Noji, Akihiro Inazu, Toshinori Higashikata, et al.
Pageof 9