Kosuke Hosoba
Hiroshima, Japan
Last Updated: 09/26/2026
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Found 12 publications
Cholesterol ensures ciliary polycystin-2 localization to prevent polycystic kidney disease.
Journal: Life science alliance
Published: September 26, 2024
High-efficient CRISPR/Cas9-mediated gene targeting to establish cell models of ciliopathies.
Journal: Methods in cell biology
Published: March 26, 2023
Cholesterol in the ciliary membrane as a therapeutic target against cancer.
Journal: Frontiers in molecular biosciences
Published: February 07, 2023
Generation of a novel disease model mouse for mucopolysaccharidosis type VI via c. 252T>C human ARSB mutation knock-in.
Journal: Biochemistry and biophysics reports
Published: June 13, 2022
Imaging of the Ciliary Cholesterol Underlying the Sonic Hedgehog Signal Transduction.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: September 25, 2021
Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome.
Journal: The EMBO journal
Published: September 22, 2019
Cytoskeleton-related regulation of primary cilia shortening mediated by melanin-concentrating hormone receptor 1.
Journal: General and comparative endocrinology
Published: June 19, 2017
PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation.
Journal: Human molecular genetics
Published: June 05, 2017
Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.
Journal: Scientific reports
Published: March 06, 2017
Phosphorylation of myosin II regulatory light chain by ZIP kinase is responsible for cleavage furrow ingression during cell division in mammalian cultured cells.
Journal: Biochemical and biophysical research communications
Published: February 20, 2015
The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation.
Journal: Cell reports
Published: July 02, 2014
TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 18, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026