Showing results (111-120 of 193) with videos related to
Sort By:
Pageof 20
Mitochondrion|May 23, 2009
Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disordersMasakazu Mimaki, Hideyuki Hatakeyama, Takashi Ichiyama, et al.The International Journal of Neuropsychopharmacology|October 18, 2017
Plasma Nervonic Acid Is a Potential Biomarker for Major Depressive Disorder: A Pilot StudyYuki Kageyama, Takaoki Kasahara, Takemichi Nakamura, et al.Behavioural Brain Research|October 10, 2012
Behavioral and cortical EEG evaluations confirm the roles of both CCKA and CCKB receptors in mouse CCK-induced anxietyHeng Li, Hidenobu Ohta, Hitomi Izumi, et al.BMC Neurology|December 15, 2017
Isolated and repeated stroke-like episodes in a middle-aged man with a mitochondrial ND3 T10158C mutation: a case reportSatomi Mezuki, Kenji Fukuda, Tomonaga Matsushita, et al.Journal of the Neurological Sciences|July 5, 2011
Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutationEri Takeshita, Yoshiaki Saito, Eiji Nakagawa, et al.Nature Chemical Biology|November 10, 2020
Chemical reversal of abnormalities in cells carrying mitochondrial DNA mutationsHiroki Kobayashi, Hideyuki Hatakeyama, Haruna Nishimura, et al.Stem Cells International|May 12, 2017
Induction of Pluripotent Stem Cells from a Manifesting Carrier of Duchenne Muscular Dystrophy and Characterization of Their X-Inactivation StatusYuko Miyagoe-Suzuki, Takashi Nishiyama, Miho Nakamura, et al.Nature Communications|February 7, 2025
Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosisShunsuke Funaguma, Aritoshi Iida, Yoshihiko Saito, et al.Journal of the Neurological Sciences|October 7, 2009
Activation of microglia/macrophages expressing phosphorylated S6 ribosomal protein in a case of hemimegalencephaly with progressive calcification and atrophyYutaka Nonoda, Yoshiaki Saito, Masayuki Itoh, et al.Neuropediatrics|August 2, 2019
Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case ReportAyaka Hirasawa-Inoue, Eri Takeshita, Yuko Shimizu-Motohashi, et al.Pageof 20