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Noriko Miyake

Showing results (61-70 of 463) with videos related to

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Human Genome Variation|May 26, 2018
A novel 8-bp duplication in <i>ADAT3</i> causes mild intellectual disabilityAhmad Reza Salehi Chaleshtori, Noriko Miyake, Mohammad Ahmadvand, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndromeNoriko Miyake, Caroline Andrews, Wen Fan, et al.
The Journal of Gene Medicine|April 2, 2009
Global diffuse distribution in the brain and efficient gene delivery to the dorsal root ganglia by intrathecal injection of adeno-associated viral vector serotype 1Naotaka Iwamoto, Atsushi Watanabe, Motoko Yamamoto, et al.
Brain & Development|October 22, 2021
Polymicrogyria in a child with KCNMA1-related channelopathyDenis Graber, Eri Imagawa, Noriko Miyake, et al.
Internal Medicine (Tokyo, Japan)|August 16, 2012
A novel SACS mutation in an atypical case with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)Satoko Miyatake, Noriko Miyake, Hiroshi Doi, et al.
American Journal of Medical Genetics. Part A|October 10, 2023
Craniosynostosis in molecularly diagnosed Kabuki syndrome: Prevalence and clinical implicationsEriko Nishi, Noriko Miyake, Rie Kawamura, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
NUP107 mutations in children with steroid-resistant nephrotic syndromeEujin Park, Yo Han Ahn, Hee Gyung Kang, et al.
Biological & Pharmaceutical Bulletin|September 3, 2019
Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome PatientsKazuo Yamada, Atsushi Watanabe, Haruo Takeshita, et al.
Stem Cells (Dayton, Ohio)|October 8, 2005
HOXB4-induced self-renewal of hematopoietic stem cells is significantly enhanced by p21 deficiencyNoriko Miyake, Ann C M Brun, Mattias Magnusson, et al.
Clinical Genetics|September 14, 2018
New SMARCE1 variant in a patient with features overlapping with oculoauriculofrontonasal syndromeShoji Yano, Atsuko Fujimoto, Jeanne Morin-Leisk, et al.
Pageof 47

Showing results (61-70 of 463) with videos related to

Sort By:
Pageof 47
Human Genome Variation|May 26, 2018
A novel 8-bp duplication in <i>ADAT3</i> causes mild intellectual disabilityAhmad Reza Salehi Chaleshtori, Noriko Miyake, Mohammad Ahmadvand, et al.
American Journal of Medical Genetics. Part A|December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndromeNoriko Miyake, Caroline Andrews, Wen Fan, et al.
The Journal of Gene Medicine|April 2, 2009
Global diffuse distribution in the brain and efficient gene delivery to the dorsal root ganglia by intrathecal injection of adeno-associated viral vector serotype 1Naotaka Iwamoto, Atsushi Watanabe, Motoko Yamamoto, et al.
Brain & Development|October 22, 2021
Polymicrogyria in a child with KCNMA1-related channelopathyDenis Graber, Eri Imagawa, Noriko Miyake, et al.
Internal Medicine (Tokyo, Japan)|August 16, 2012
A novel SACS mutation in an atypical case with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)Satoko Miyatake, Noriko Miyake, Hiroshi Doi, et al.
American Journal of Medical Genetics. Part A|October 10, 2023
Craniosynostosis in molecularly diagnosed Kabuki syndrome: Prevalence and clinical implicationsEriko Nishi, Noriko Miyake, Rie Kawamura, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
NUP107 mutations in children with steroid-resistant nephrotic syndromeEujin Park, Yo Han Ahn, Hee Gyung Kang, et al.
Biological & Pharmaceutical Bulletin|September 3, 2019
Measurement of Serum Tenascin-X in Joint Hypermobility Syndrome PatientsKazuo Yamada, Atsushi Watanabe, Haruo Takeshita, et al.
Stem Cells (Dayton, Ohio)|October 8, 2005
HOXB4-induced self-renewal of hematopoietic stem cells is significantly enhanced by p21 deficiencyNoriko Miyake, Ann C M Brun, Mattias Magnusson, et al.
Clinical Genetics|September 14, 2018
New SMARCE1 variant in a patient with features overlapping with oculoauriculofrontonasal syndromeShoji Yano, Atsuko Fujimoto, Jeanne Morin-Leisk, et al.
Pageof 47