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Journal of Drug Targeting|July 3, 2015
Non-invasive gene targeting to the fetal brain after intravenous administration and transplacental transfer of plasmid DNA using PEGylated immunoliposomesEain M Cornford, Shigeyo Hyman, Marcia E Cornford, et al.Elife|May 23, 2023
<i>Scn1a</i>-GFP transgenic mouse revealed Nav1.1 expression in neocortical pyramidal tract projection neuronsTetsushi Yamagata, Ikuo Ogiwara, Tetsuya Tatsukawa, et al.Molecular and Cellular Neurosciences|April 18, 2026
Myoclonin1 haploinsufficiency in motile ciliated cells partially recapitulates epileptic features of Efhc1-deficient mice in adult ageToshimitsu Suzuki, Tetsuya Tatsukawa, Genki Sudo, et al.Epilepsia|April 29, 2021
Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24Toshimitsu Suzuki, Yoshinao Koike, Kyota Ashikawa, et al.Journal of Gastroenterology and Hepatology|October 26, 2005
Comparative study of diagnostic value of cytologic sampling by endoscopic ultrasonography-guided fine-needle aspiration and that by endoscopic retrograde pancreatography for the management of pancreatic mass without biliary strictureTakeru Wakatsuki, Atsushi Irisawa, Manoop S Bhutani, et al.Journal of Human Genetics|July 16, 2005
Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese populationShweta Singh, Toshimitsu Suzuki, Akira Uchiyama, et al.Hepato-Gastroenterology|May 18, 2004
Variceal recurrence after endoscopic sclerotherapy associated with the perforating veins in lower esophagus independentlyGoro Shibukawa, Atsushi Irisawa, Ayako Saito, et al.Human Molecular Genetics|January 17, 2009
Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibilityToshimitsu Suzuki, Hiroyuki Miyamoto, Takashi Nakahari, et al.Nature Communications|April 25, 2019
Impaired cortico-striatal excitatory transmission triggers epilepsyHiroyuki Miyamoto, Tetsuya Tatsukawa, Atsushi Shimohata, et al.Human Mutation|April 3, 2007
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. OnlineBaljinder Singh, Arnaud Monteil, Isabelle Bidaud, et al.Pageof 9