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Masaaki Furuno

Showing results (1-10 of 29) with videos related to

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Seikagaku. the Journal of Japanese Biochemical Society|April 16, 2003
[FANTOM-DB: database of functional annotation of RIKEN mouse cDNA clones]Hidemasa Bono, Takeya Kasukawa, Masaaki Furuno, et al.
Nucleic Acids Research|December 26, 2001
FANTOM DB: database of Functional Annotation of RIKEN Mouse cDNA ClonesHidemasa Bono, Takeya Kasukawa, Masaaki Furuno, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 6, 2011
Competition between a noncoding exon and introns: Gomafu contains tandem UACUAAC repeats and associates with splicing factor-1Hitomi Tsuiji, Rei Yoshimoto, Yuko Hasegawa, et al.
Microbiology (Reading, England)|March 13, 2021
Characterization of polar-flagellar-length mutants in <i>Vibrio alginolyticus</i>Masaaki Furuno, Tatsuo Atsumi, Taku Yamada, et al.
Scientific Reports|November 28, 2019
A framework for identification of on- and off-target transcriptional responses to drug treatmentYi Huang, Masaaki Furuno, Takahiro Arakawa, et al.
Genome Research|June 24, 2003
CDS annotation in full-length cDNA sequenceMasaaki Furuno, Takeya Kasukawa, Rintaro Saito, et al.
BMC Bioinformatics|January 11, 2023
xcore: an R package for inference of gene expression regulatorsMaciej Migdał, Takahiro Arakawa, Satoshi Takizawa, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 2, 2015
Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutationsKazuki Kuniyoshi, Hiroyuki Sakuramoto, Kazutoshi Yoshitake, et al.
Molecular Vision|December 10, 2013
Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndromeSatoshi Katagiri, Kazutoshi Yoshitake, Masakazu Akahori, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 23, 2014
Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutationKazuki Kuniyoshi, Hiroyuki Sakuramoto, Kazutoshi Yoshitake, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Seikagaku. the Journal of Japanese Biochemical Society|April 16, 2003
[FANTOM-DB: database of functional annotation of RIKEN mouse cDNA clones]Hidemasa Bono, Takeya Kasukawa, Masaaki Furuno, et al.
Nucleic Acids Research|December 26, 2001
FANTOM DB: database of Functional Annotation of RIKEN Mouse cDNA ClonesHidemasa Bono, Takeya Kasukawa, Masaaki Furuno, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|April 6, 2011
Competition between a noncoding exon and introns: Gomafu contains tandem UACUAAC repeats and associates with splicing factor-1Hitomi Tsuiji, Rei Yoshimoto, Yuko Hasegawa, et al.
Microbiology (Reading, England)|March 13, 2021
Characterization of polar-flagellar-length mutants in <i>Vibrio alginolyticus</i>Masaaki Furuno, Tatsuo Atsumi, Taku Yamada, et al.
Scientific Reports|November 28, 2019
A framework for identification of on- and off-target transcriptional responses to drug treatmentYi Huang, Masaaki Furuno, Takahiro Arakawa, et al.
Genome Research|June 24, 2003
CDS annotation in full-length cDNA sequenceMasaaki Furuno, Takeya Kasukawa, Rintaro Saito, et al.
BMC Bioinformatics|January 11, 2023
xcore: an R package for inference of gene expression regulatorsMaciej Migdał, Takahiro Arakawa, Satoshi Takizawa, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 2, 2015
Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutationsKazuki Kuniyoshi, Hiroyuki Sakuramoto, Kazutoshi Yoshitake, et al.
Molecular Vision|December 10, 2013
Whole-exome sequencing identifies a novel ALMS1 mutation (p.Q2051X) in two Japanese brothers with Alström syndromeSatoshi Katagiri, Kazutoshi Yoshitake, Masakazu Akahori, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 23, 2014
Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutationKazuki Kuniyoshi, Hiroyuki Sakuramoto, Kazutoshi Yoshitake, et al.
Pageof 3