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Journal of Neurosurgery. Pediatrics
|
October 22, 2016
Maternal administration of meclozine for the treatment of foramen magnum stenosis in transgenic mice with achondroplasia
Masaki Matsushita, Kenichi Mishima, Ryusaku Esaki, et al.
Redox Report : Communications in Free Radical Research
|
February 12, 2016
Molecular hydrogen alleviates motor deficits and muscle degeneration in mdx mice
Satoru Hasegawa, Mikako Ito, Mayu Fukami, et al.
Molecular and Cellular Biochemistry
|
November 7, 2012
S100A10 is required for the organization of actin stress fibers and promotion of cell spreading
Shurovi Sayeed, Eri Asano, Satoko Ito, et al.
Human Molecular Genetics
|
March 26, 2003
E-box mutations in the RAPSN promoter region in eight cases with congenital myasthenic syndrome
Kinji Ohno, Menachem Sadeh, Ilan Blatt, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
January 21, 2020
[Electrophysiological evidence of impaired neuromuscular junction in a case of phosphoglucomutase 1 deficiency manifesting fluctuating muscle weakness]
Yu Takenaka, Kenji Sekiguchi, Hiroaki Sekiya, et al.
Biochemical and Biophysical Research Communications
|
August 6, 2014
LRP4 induces extracellular matrix productions and facilitates chondrocyte differentiation
Nobuyuki Asai, Bisei Ohkawara, Mikako Ito, et al.
Plos One
|
June 23, 2012
The unstable CCTG repeat responsible for myotonic dystrophy type 2 originates from an AluSx element insertion into an early primate genome
Tatsuaki Kurosaki, Shintaroh Ueda, Takafumi Ishida, et al.
CEN Case Reports
|
February 6, 2025
Case of maternal uniparental isodisomy with autosomal recessive Alport syndrome combined with congenital myasthenia and Oguchi disease
Misaki Akiyama, Keiko Matsubara, Hiroshi Terashima, et al.
Scientific Reports
|
August 9, 2017
Clinical dosage of meclozine promotes longitudinal bone growth, bone volume, and trabecular bone quality in transgenic mice with achondroplasia
Masaki Matsushita, Ryusaku Esaki, Kenichi Mishima, et al.
Muscle & Nerve
|
July 2, 2026
Review of Congenital Myasthenic Syndrome Caused by Pathogenic Variants in GFPT1
Kinji Ohno, Mohammad Nazim, Ruchen Zhang, et al.
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of 25
Search research articles
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Showing results (71-80 of 245) with videos related to
Sort By:
Page
of 25
Journal of Neurosurgery. Pediatrics
|
October 22, 2016
Maternal administration of meclozine for the treatment of foramen magnum stenosis in transgenic mice with achondroplasia
Masaki Matsushita, Kenichi Mishima, Ryusaku Esaki, et al.
Redox Report : Communications in Free Radical Research
|
February 12, 2016
Molecular hydrogen alleviates motor deficits and muscle degeneration in mdx mice
Satoru Hasegawa, Mikako Ito, Mayu Fukami, et al.
Molecular and Cellular Biochemistry
|
November 7, 2012
S100A10 is required for the organization of actin stress fibers and promotion of cell spreading
Shurovi Sayeed, Eri Asano, Satoko Ito, et al.
Human Molecular Genetics
|
March 26, 2003
E-box mutations in the RAPSN promoter region in eight cases with congenital myasthenic syndrome
Kinji Ohno, Menachem Sadeh, Ilan Blatt, et al.
Rinsho Shinkeigaku = Clinical Neurology
|
January 21, 2020
[Electrophysiological evidence of impaired neuromuscular junction in a case of phosphoglucomutase 1 deficiency manifesting fluctuating muscle weakness]
Yu Takenaka, Kenji Sekiguchi, Hiroaki Sekiya, et al.
Biochemical and Biophysical Research Communications
|
August 6, 2014
LRP4 induces extracellular matrix productions and facilitates chondrocyte differentiation
Nobuyuki Asai, Bisei Ohkawara, Mikako Ito, et al.
Plos One
|
June 23, 2012
The unstable CCTG repeat responsible for myotonic dystrophy type 2 originates from an AluSx element insertion into an early primate genome
Tatsuaki Kurosaki, Shintaroh Ueda, Takafumi Ishida, et al.
CEN Case Reports
|
February 6, 2025
Case of maternal uniparental isodisomy with autosomal recessive Alport syndrome combined with congenital myasthenia and Oguchi disease
Misaki Akiyama, Keiko Matsubara, Hiroshi Terashima, et al.
Scientific Reports
|
August 9, 2017
Clinical dosage of meclozine promotes longitudinal bone growth, bone volume, and trabecular bone quality in transgenic mice with achondroplasia
Masaki Matsushita, Ryusaku Esaki, Kenichi Mishima, et al.
Muscle & Nerve
|
July 2, 2026
Review of Congenital Myasthenic Syndrome Caused by Pathogenic Variants in GFPT1
Kinji Ohno, Mohammad Nazim, Ruchen Zhang, et al.
Page
of 25