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Ryo Funayama

Showing results (41-50 of 79) with videos related to

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Annals of Hematology|May 1, 2014
Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemiaTohru Fujiwara, Noriko Fukuhara, Ryo Funayama, et al.
Iscience|April 17, 2020
The Autism-Related Protein SETD5 Controls Neural Cell Proliferation through Epigenetic Regulation of rDNA ExpressionTadashi Nakagawa, Satoko Hattori, Risa Nobuta, et al.
Journal of Human Genetics|March 21, 2021
A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathyAya Inoue-Shibui, Tetsuya Niihori, Michio Kobayashi, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Mutations in PIGL in a patient with Mabry syndromeIkuma Fujiwara, Yoshiko Murakami, Tetsuya Niihori, et al.
Journal of Human Genetics|March 1, 2013
Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failureRumiko Izumi, Tetsuya Niihori, Yoko Aoki, et al.
Human Molecular Genetics|October 10, 2013
RNA sequencing-based identification of aberrant imprinting in cloned miceHiroaki Okae, Shogo Matoba, Takeshi Nagashima, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2013
Y chromosome-linked B and NK cell deficiency in miceShu-lan Sun, Satoshi Horino, Ari Itoh-Nakadai, et al.
Cell Reports|March 9, 2017
A Bach2-Cebp Gene Regulatory Network for the Commitment of Multipotent Hematopoietic ProgenitorsAri Itoh-Nakadai, Mitsuyo Matsumoto, Hiroki Kato, et al.
Neurology. Genetics|April 12, 2016
Isolated inclusion body myopathy caused by a multisystem proteinopathy-linked hnRNPA1 mutationRumiko Izumi, Hitoshi Warita, Tetsuya Niihori, et al.
Brain & Development|February 4, 2018
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutationHaruhiko Nakamura, Mitsugu Uematsu, Yurika Numata-Uematsu, et al.
Pageof 8

Showing results (41-50 of 79) with videos related to

Sort By:
Pageof 8
Annals of Hematology|May 1, 2014
Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemiaTohru Fujiwara, Noriko Fukuhara, Ryo Funayama, et al.
Iscience|April 17, 2020
The Autism-Related Protein SETD5 Controls Neural Cell Proliferation through Epigenetic Regulation of rDNA ExpressionTadashi Nakagawa, Satoko Hattori, Risa Nobuta, et al.
Journal of Human Genetics|March 21, 2021
A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathyAya Inoue-Shibui, Tetsuya Niihori, Michio Kobayashi, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Mutations in PIGL in a patient with Mabry syndromeIkuma Fujiwara, Yoshiko Murakami, Tetsuya Niihori, et al.
Journal of Human Genetics|March 1, 2013
Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failureRumiko Izumi, Tetsuya Niihori, Yoko Aoki, et al.
Human Molecular Genetics|October 10, 2013
RNA sequencing-based identification of aberrant imprinting in cloned miceHiroaki Okae, Shogo Matoba, Takeshi Nagashima, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2013
Y chromosome-linked B and NK cell deficiency in miceShu-lan Sun, Satoshi Horino, Ari Itoh-Nakadai, et al.
Cell Reports|March 9, 2017
A Bach2-Cebp Gene Regulatory Network for the Commitment of Multipotent Hematopoietic ProgenitorsAri Itoh-Nakadai, Mitsuyo Matsumoto, Hiroki Kato, et al.
Neurology. Genetics|April 12, 2016
Isolated inclusion body myopathy caused by a multisystem proteinopathy-linked hnRNPA1 mutationRumiko Izumi, Hitoshi Warita, Tetsuya Niihori, et al.
Brain & Development|February 4, 2018
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutationHaruhiko Nakamura, Mitsugu Uematsu, Yurika Numata-Uematsu, et al.
Pageof 8