Masaaki Furuno

Yokohama, 2300045, Japan

Last Updated: 09/26/2026

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Found 16 publications

xcore: an R package for inference of gene expression regulators.

xcore: an R package for inference of gene expression regulators.

Journal: BMC bioinformatics

Published: July 03, 2022

Development of p53 knockout U87MG cell line for unbiased drug delivery testing system using CRISPR-Cas9 and transcriptomic analysis.

Development of p53 knockout U87MG cell line for unbiased drug delivery testing system using CRISPR-Cas9 and transcriptomic analysis.

Journal: Journal of biotechnology

Published: October 06, 2020

Spliceostatin A interaction with SF3B limits U1 snRNP availability and causes premature cleavage and polyadenylation.

Spliceostatin A interaction with SF3B limits U1 snRNP availability and causes premature cleavage and polyadenylation.

Journal: Cell chemical biology

Published: September 03, 2020

A framework for identification of on- and off-target transcriptional responses to drug treatment.

A framework for identification of on- and off-target transcriptional responses to drug treatment.

Journal: Scientific reports

Published: September 02, 2019

C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution.

C1 CAGE detects transcription start sites and enhancer activity at single-cell resolution.

Journal: Nature communications

Published: June 11, 2018

CD157 Marks Tissue-Resident Endothelial Stem Cells with Homeostatic and Regenerative Properties.

CD157 Marks Tissue-Resident Endothelial Stem Cells with Homeostatic and Regenerative Properties.

Journal: Cell stem cell

Published: May 31, 2017

FANTOM5 CAGE profiles of human and mouse samples.

FANTOM5 CAGE profiles of human and mouse samples.

Journal: Scientific data

Published: December 06, 2016

Global analysis of pre-mRNA subcellular localization following splicing inhibition by spliceostatin A.

Global analysis of pre-mRNA subcellular localization following splicing inhibition by spliceostatin A.

Journal: RNA (New York, N.Y.)

Published: June 26, 2016

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability.

CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability.

Journal: Scientific reports

Published: March 17, 2016

Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K).

Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K).

Journal: Ophthalmic genetics

Published: January 22, 2015

RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.

RHO Mutations (p.W126L and p.A346P) in Two Japanese Families with Autosomal Dominant Retinitis Pigmentosa.

Journal: Journal of ophthalmology

Published: July 26, 2014

Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy.

Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: June 25, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026