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Science Advances|February 1, 2021
CGG repeat RNA G-quadruplexes interact with FMRpolyG to cause neuronal dysfunction in fragile X-related tremor/ataxia syndromeSefan Asamitsu, Yasushi Yabuki, Susumu Ikenoshita, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 1, 2005
Subtype switching of T-type Ca 2+ channels from Cav3.2 to Cav3.1 during differentiation of embryonic stem cells to cardiac cell lineageEinosuke Mizuta, Junichiro Miake, Shuichi Yano, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|April 6, 2007
No association between the neuronal pentraxin II gene polymorphism and autismTetsuya Marui, Shinko Koishi, Ikuko Funatogawa, et al.
Yonago Acta Medica|April 10, 2019
Recurrent Erythema Nodosum in a Child with a SHOC2 Gene MutationTetsuya Okazaki, Yoshiaki Saito, Kazunari Sugita, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|January 14, 2021
[Successful treatment with enzyme replacement therapy for pelvic fragile fracture in an elderly case of type I Gaucher's disease]Chisato Matsubara, Kazuhiko Yamamoto, Takeshi Maeda, et al.
Biochemical and Biophysical Research Communications|September 28, 2005
Evidence for proteasomal degradation of Kv1.5 channel proteinMasaru Kato, Kazuyoshi Ogura, Junichiro Miake, et al.
Biochemical and Biophysical Research Communications|February 27, 2003
Coordinate induction of AMP deaminase in human atrium with mitochondrial DNA deletionYoko Tomikura, Ichiro Hisatome, Mariko Tsuboi, et al.
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