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

A Ohtake

Showing results (51-60 of 65) with videos related to

Pageof 7
Sort By:
FEBS Letters|February 28, 2001
Role of Thr(11) in the binding of omega-conotoxin MVIIC to N-type Ca2+ channelsK Minami, C Raymond, N Martin-Moutot, et al.
Biochemical and Biophysical Research Communications|March 1, 2000
Binding of six chimeric analogs of omega-conotoxin MVIIA and MVIIC to N- and P/Q-type calcium channelsK Sato, C Raymond, N Martin-Moutot, et al.
Clinical Genetics|March 28, 2008
Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiencyT Yasuno, H Kaneoka, T Tokuyasu, et al.
FEBS Letters|October 7, 1997
Binding of chimeric analogs of omega-conotoxin MVIIA and MVIIC to the N- and P/Q-type calcium channelsK Sato, C Raymond, N Martin-Moutot, et al.
FEBS Letters|March 14, 2000
Binding of Ala-scanning analogs of omega-conotoxin MVIIC to N- and P/Q-type calcium channelsK Sato, C Raymond, N Martin-Moutot, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 14, 2018
Estimation of glycaemic control in the past month using ratio of glycated albumin to HbA<sub>1c</sub>I Musha, M Mochizuki, T Kikuchi, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 30, 1999
Indian childhood cirrhosis-like disease in a Japanese boy undergoing liver transplantationH Nagasaka, K Kobayashi, T Yorifuji, et al.
Human Genetics|July 1, 1996
Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiencyS Yamamoto, H Abe, T Kohgo, et al.
Clinical Genetics|June 9, 2017
Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial-RNA-import protein PNPase cause delayed myelinationR Sato, N Arai-Ichinoi, A Kikuchi, et al.
European Journal of Pediatrics|March 26, 2003
Two cases with transient lipoprotein lipase (LPL) activity impairment: evidence for the possible involvement of an LPL inhibitorH Nagasaka, H Kikuta, H Chiba, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
FEBS Letters|February 28, 2001
Role of Thr(11) in the binding of omega-conotoxin MVIIC to N-type Ca2+ channelsK Minami, C Raymond, N Martin-Moutot, et al.
Biochemical and Biophysical Research Communications|March 1, 2000
Binding of six chimeric analogs of omega-conotoxin MVIIA and MVIIC to N- and P/Q-type calcium channelsK Sato, C Raymond, N Martin-Moutot, et al.
Clinical Genetics|March 28, 2008
Mutations of carnitine palmitoyltransferase II (CPT II) in Japanese patients with CPT II deficiencyT Yasuno, H Kaneoka, T Tokuyasu, et al.
FEBS Letters|October 7, 1997
Binding of chimeric analogs of omega-conotoxin MVIIA and MVIIC to the N- and P/Q-type calcium channelsK Sato, C Raymond, N Martin-Moutot, et al.
FEBS Letters|March 14, 2000
Binding of Ala-scanning analogs of omega-conotoxin MVIIC to N- and P/Q-type calcium channelsK Sato, C Raymond, N Martin-Moutot, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 14, 2018
Estimation of glycaemic control in the past month using ratio of glycated albumin to HbA<sub>1c</sub>I Musha, M Mochizuki, T Kikuchi, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 30, 1999
Indian childhood cirrhosis-like disease in a Japanese boy undergoing liver transplantationH Nagasaka, K Kobayashi, T Yorifuji, et al.
Human Genetics|July 1, 1996
Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiencyS Yamamoto, H Abe, T Kohgo, et al.
Clinical Genetics|June 9, 2017
Novel biallelic mutations in the PNPT1 gene encoding a mitochondrial-RNA-import protein PNPase cause delayed myelinationR Sato, N Arai-Ichinoi, A Kikuchi, et al.
European Journal of Pediatrics|March 26, 2003
Two cases with transient lipoprotein lipase (LPL) activity impairment: evidence for the possible involvement of an LPL inhibitorH Nagasaka, H Kikuta, H Chiba, et al.
Pageof 7