Showing results (91-100 of 301) with videos related to
Sort By:
Pageof 31
Rinsho Shinkeigaku = Clinical Neurology|January 21, 2020
[Electrophysiological evidence of impaired neuromuscular junction in a case of phosphoglucomutase 1 deficiency manifesting fluctuating muscle weakness]Yu Takenaka, Kenji Sekiguchi, Hiroaki Sekiya, et al.Biochemical and Biophysical Research Communications|August 6, 2014
LRP4 induces extracellular matrix productions and facilitates chondrocyte differentiationNobuyuki Asai, Bisei Ohkawara, Mikako Ito, et al.Plos One|June 23, 2012
The unstable CCTG repeat responsible for myotonic dystrophy type 2 originates from an AluSx element insertion into an early primate genomeTatsuaki Kurosaki, Shintaroh Ueda, Takafumi Ishida, et al.CEN Case Reports|February 6, 2025
Case of maternal uniparental isodisomy with autosomal recessive Alport syndrome combined with congenital myasthenia and Oguchi diseaseMisaki Akiyama, Keiko Matsubara, Hiroshi Terashima, et al.Scientific Reports|August 9, 2017
Clinical dosage of meclozine promotes longitudinal bone growth, bone volume, and trabecular bone quality in transgenic mice with achondroplasiaMasaki Matsushita, Ryusaku Esaki, Kenichi Mishima, et al.Muscle & Nerve|July 2, 2026
Review of Congenital Myasthenic Syndrome Caused by Pathogenic Variants in GFPT1Kinji Ohno, Mohammad Nazim, Ruchen Zhang, et al.Current Opinion in Pharmacology|May 24, 2005
Current understanding of congenital myasthenic syndromesAndrew G Engel, Steven M SineNature|March 24, 2006
Recent advances in Cys-loop receptor structure and functionSteven M Sine, Andrew G EngelScientific Reports|November 29, 2022
Efficacy of soluble lansoprazole-impregnated beta-tricalcium phosphate for bone regenerationKenichi Mishima, Yuka Tsukagoshi Okabe, Masaaki Mizuno, et al.Molecular Cell|July 25, 2024
Blending and separating dynamics of RNA-binding proteins develop architectural splicing networks spreading throughout the nucleusAkio Masuda, Takaaki Okamoto, Toshihiko Kawachi, et al.Pageof 31