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Fuyuki Miya

Showing results (31-40 of 109) with videos related to

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Journal of Human Genetics|September 26, 2014
KIF1A mutation in a patient with progressive neurodegenerationNobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 23, 2014
Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3Atsuko Harada, Fuyuki Miya, Hidetsuna Utsunomiya, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 29, 2021
Four pedigrees with aminoacyl-tRNA synthetase abnormalitiesNobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, et al.
Endocrinology|February 10, 2011
Growth hormone-dependent pathogenesis of human hepatic steatosis in a novel mouse model bearing a human hepatocyte-repopulated liverChise Tateno, Miho Kataoka, Rie Utoh, et al.
Cancer Medicine|May 26, 2017
The prediction models for postoperative overall survival and disease-free survival in patients with breast cancerDaichi Shigemizu, Takuji Iwase, Masataka Yoshimoto, et al.
Human Genome Variation|July 6, 2021
Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetesJun Hosoe, Ken Suzuki, Fuyuki Miya, et al.
American Journal of Medical Genetics. Part A|February 16, 2018
Cover Image, Volume 176A, Number 3, March 2018Kei Tamai, Katsuhiko Tada, Akihito Takeuchi, et al.
American Journal of Medical Genetics. Part A|January 18, 2018
Fetal ultrasonographic findings including cerebral hyperechogenicity in a patient with non-lethal form of Raine syndromeKei Tamai, Katsuhiko Tada, Akihito Takeuchi, et al.
Brain & Development|June 7, 2021
Two cases of DYNC1H1 mutations with intractable epilepsyAyumi Matsumoto, Karin Kojima, Fuyuki Miya, et al.
Developmental Cell|November 6, 2024
Comparative analysis of tongue cancer organoids among patients identifies the heritable nature of minimal residual diseaseMiwako Sase, Taku Sato, Hajime Sato, et al.
Pageof 11

Showing results (31-40 of 109) with videos related to

Sort By:
Pageof 11
Journal of Human Genetics|September 26, 2014
KIF1A mutation in a patient with progressive neurodegenerationNobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|November 23, 2014
Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3Atsuko Harada, Fuyuki Miya, Hidetsuna Utsunomiya, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 29, 2021
Four pedigrees with aminoacyl-tRNA synthetase abnormalitiesNobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, et al.
Endocrinology|February 10, 2011
Growth hormone-dependent pathogenesis of human hepatic steatosis in a novel mouse model bearing a human hepatocyte-repopulated liverChise Tateno, Miho Kataoka, Rie Utoh, et al.
Cancer Medicine|May 26, 2017
The prediction models for postoperative overall survival and disease-free survival in patients with breast cancerDaichi Shigemizu, Takuji Iwase, Masataka Yoshimoto, et al.
Human Genome Variation|July 6, 2021
Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetesJun Hosoe, Ken Suzuki, Fuyuki Miya, et al.
American Journal of Medical Genetics. Part A|February 16, 2018
Cover Image, Volume 176A, Number 3, March 2018Kei Tamai, Katsuhiko Tada, Akihito Takeuchi, et al.
American Journal of Medical Genetics. Part A|January 18, 2018
Fetal ultrasonographic findings including cerebral hyperechogenicity in a patient with non-lethal form of Raine syndromeKei Tamai, Katsuhiko Tada, Akihito Takeuchi, et al.
Brain & Development|June 7, 2021
Two cases of DYNC1H1 mutations with intractable epilepsyAyumi Matsumoto, Karin Kojima, Fuyuki Miya, et al.
Developmental Cell|November 6, 2024
Comparative analysis of tongue cancer organoids among patients identifies the heritable nature of minimal residual diseaseMiwako Sase, Taku Sato, Hajime Sato, et al.
Pageof 11