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Brain & Development|September 6, 2025
Fukuyama congenital muscular dystrophy: Clinical features and therapeutic advancesKeiko Ishigaki, Mariko Taniguchi-Ikeda
Molecular Aspects of Medicine|July 17, 2016
Mechanistic aspects of the formation of α-dystroglycan and therapeutic research for the treatment of α-dystroglycanopathy: A reviewMariko Taniguchi-Ikeda, Ichiro Morioka, Kazumoto Iijima, et al.
Stem Cells Translational Medicine|November 23, 2017
The Generation of Human γδT Cell-Derived Induced Pluripotent Stem Cells from Whole Peripheral Blood Mononuclear Cell CultureDaisuke Watanabe, Michiyo Koyanagi-Aoi, Mariko Taniguchi-Ikeda, et al.
Human Genome Variation|September 23, 2016
A 12p13 GRIN2B deletion is associated with developmental delay and macrocephalyNaoya Morisada, Tomoaki Ioroi, Mariko Taniguchi-Ikeda, et al.
Journal of Human Genetics|July 7, 2017
Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in JapanKazuhiro Kobayashi, Reiko Kato, Eri Kondo-Iida, et al.
JACS Au|June 28, 2024
Molecular Aggregation Strategy for Inhibiting DNasesKenta Morita, Tomoko Moriwaki, Shunsuke Habe, et al.
Clinical Laboratory|February 7, 2017
Periomphalitis with Delayed Umbilical Cord Separation due to Alloimmune Neonatal NeutropeniaTomohiro Sameshima, Sota Iwatani, Sachiyo Fukushima, et al.
Pigment Cell & Melanoma Research|March 8, 2019
Induced pluripotent stem cell-derived melanocyte precursor cells undergoing differentiation into melanocytesChieko Hosaka, Makoto Kunisada, Michiyo Koyanagi-Aoi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|June 28, 2016
Comprehensive analysis of serum cytokines/chemokines in febrile children with primary human herpes virus-6B infectionMiwako Nagasaka, Ichiro Morioka, Akiko Kawabata, et al.
Human Molecular Genetics|November 25, 2022
Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variantSarantuya Enkhjargal, Kana Sugahara, Behnoush Khaledian, et al.
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