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Hiroko Shimbo

Showing results (21-30 of 37) with videos related to

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Pharmaceutical Research|March 4, 2020
Cyclocreatine Transport by SLC6A8, the Creatine Transporter, in HEK293 Cells, a Human Blood-Brain Barrier Model Cell, and CCDSs Patient-Derived FibroblastsTatsuki Uemura, Shingo Ito, Takeshi Masuda, et al.
Surgery Today|September 3, 2020
A novel method for isolating lymphatic endothelial cells from lymphatic malformations and detecting PIK3CA somatic mutation in these isolated cellsHidehito Usui, Yoshinori Tsurusaki, Hiroko Shimbo, et al.
Molecular Genetics & Genomic Medicine|July 19, 2017
Haploinsufficiency of <i>BCL11A</i> associated with cerebellar abnormalities in 2p15p16.1 deletion syndromeHiroko Shimbo, Takayuki Yokoi, Noriko Aida, et al.
Annals of Neurology|August 10, 2010
Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus-Merzbacher-like diseaseHitoshi Osaka, Haruka Hamanoue, Ryoko Yamamoto, et al.
Pediatric Neurology|March 18, 2014
A novel two-nucleotide deletion in the ATP7A gene associated with delayed infantile onset of Menkes diseaseTakahito Wada, Marie Reine Haddad, Ling Yi, et al.
Brain & Development|September 17, 2017
Japanese Leigh syndrome case treated with EPI-743Takeshi Kouga, Mariko Takagi, Akihiko Miyauchi, et al.
Brain & Development|September 15, 2018
Aggregate formation analysis of GFAPJanyerkye Tulyeu, Moe Tamaura, Eriko Jimbo, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A rapid screening with direct sequencing from blood samples for the diagnosis of Leigh syndromeHiroko Shimbo, Mariko Takagi, Mitsuko Okuda, et al.
Brain & Development|March 14, 2012
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutationsJunpei Tanigawa, Kaori Kaneko, Masakazu Honda, et al.
Journal of Psychiatric Research|May 19, 2023
Disease specific brain capillary angiopathy in schizophrenia, bipolar disorder, and Alzheimer's diseaseShinobu Hirai, Atsuhiro Sakuma, Yasuto Kunii, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Pharmaceutical Research|March 4, 2020
Cyclocreatine Transport by SLC6A8, the Creatine Transporter, in HEK293 Cells, a Human Blood-Brain Barrier Model Cell, and CCDSs Patient-Derived FibroblastsTatsuki Uemura, Shingo Ito, Takeshi Masuda, et al.
Surgery Today|September 3, 2020
A novel method for isolating lymphatic endothelial cells from lymphatic malformations and detecting PIK3CA somatic mutation in these isolated cellsHidehito Usui, Yoshinori Tsurusaki, Hiroko Shimbo, et al.
Molecular Genetics & Genomic Medicine|July 19, 2017
Haploinsufficiency of <i>BCL11A</i> associated with cerebellar abnormalities in 2p15p16.1 deletion syndromeHiroko Shimbo, Takayuki Yokoi, Noriko Aida, et al.
Annals of Neurology|August 10, 2010
Disrupted SOX10 regulation of GJC2 transcription causes Pelizaeus-Merzbacher-like diseaseHitoshi Osaka, Haruka Hamanoue, Ryoko Yamamoto, et al.
Pediatric Neurology|March 18, 2014
A novel two-nucleotide deletion in the ATP7A gene associated with delayed infantile onset of Menkes diseaseTakahito Wada, Marie Reine Haddad, Ling Yi, et al.
Brain & Development|September 17, 2017
Japanese Leigh syndrome case treated with EPI-743Takeshi Kouga, Mariko Takagi, Akihiko Miyauchi, et al.
Brain & Development|September 15, 2018
Aggregate formation analysis of GFAPJanyerkye Tulyeu, Moe Tamaura, Eriko Jimbo, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A rapid screening with direct sequencing from blood samples for the diagnosis of Leigh syndromeHiroko Shimbo, Mariko Takagi, Mitsuko Okuda, et al.
Brain & Development|March 14, 2012
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutationsJunpei Tanigawa, Kaori Kaneko, Masakazu Honda, et al.
Journal of Psychiatric Research|May 19, 2023
Disease specific brain capillary angiopathy in schizophrenia, bipolar disorder, and Alzheimer's diseaseShinobu Hirai, Atsuhiro Sakuma, Yasuto Kunii, et al.
Pageof 4