Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|February 14, 2015
A 45,X/46,XY DSD (Disorder of Sexual Development) case with an extremely uneven distribution of 46,XY cells between lymphocytes and gonadsRisa Nomura, Kentaro Miyai, Michiyo Okada, et al.
Biochemistry and Biophysics Reports|December 25, 2019
G790del mutation in DSC2 alone is insufficient to develop the pathogenesis of ARVC in a mouse modelYoriomi Hamada, Takeshi Yamamoto, Yoshihide Nakamura, et al.
Endocrine Journal|August 23, 2016
Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patientsShigeru Takishima, Keisuke Nakajima, Risa Nomura, et al.
American Journal of Physiology. Renal Physiology|December 28, 2023
Characterization of gene expression in the kidney of renal tubular cell-specific NFAT5 knockout miceMakoto Ono, Yuichiro Izumi, Kosuke Maruyama, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 15, 2010
Dantrolene, a therapeutic agent for malignant hyperthermia, inhibits catecholaminergic polymorphic ventricular tachycardia in a RyR2(R2474S/+) knock-in mouse modelShigeki Kobayashi, Masafumi Yano, Hitoshi Uchinoumi, et al.
Journal of the American Geriatrics Society|September 6, 2008
Elevated C-reactive protein is related to cognitive decline in older adults with cardiovascular diseaseKarin F Hoth, Andreana P Haley, John Gunstad, et al.
Biochemical and Biophysical Research Communications|April 24, 2014
Enhanced binding of calmodulin to RyR2 corrects arrhythmogenic channel disorder in CPVT-associated myocytesMasakazu Fukuda, Takeshi Yamamoto, Shigehiko Nishimura, et al.
Biomolecules|August 8, 2020
Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New PatientsMakoto Ono, Don E Burgess, Elizabeth A Schroder, et al.
Pageof 10