List of works - Tatsuo Miyamoto

Albatross/FBF1 contributes to both centriole duplication and centrosome separation

scientific article published on 13 November 2018

Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders

scientific article published on 17 January 2020

Characterization of Functional Primary Cilia in Human Induced Pluripotent Stem Cell-Derived Neurons

scientific article published on 29 April 2019

Cilia play a role in breaking left-right symmetry of the sea urchin embryo.

scientific article published on 29 March 2016

Ciliary GPCR-based transcriptome as a key regulator of cilia length control

scientific article published on 05 July 2021

Ciliopathy in PCS (MVA) syndrome.

scientific article published on 22 August 2015

Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential.

scientific article

Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14

scientific article published on 01 April 2018

Cytoskeleton-related regulation of primary cilia shortening mediated by melanin-concentrating hormone receptor 1.

scientific article published on 22 August 2017

Efficient TALEN construction and evaluation methods for human cell and animal applications.

scientific article published on 6 February 2013

Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.

scientific article

Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology.

scientific article published in April 2018

Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxa

scientific article published on 20 June 2016

Generation of transgenic medaka expressing claudin7-EGFP for imaging of tight junctions in living medaka embryos.

scientific article published on 27 November 2008

Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer

scientific article published on 24 June 2020

Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.

scientific article published on 9 March 2011

Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome

scientific article published on 05 May 2020

NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations

scientific article published on 04 October 2021

PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation

scientific article published on 26 August 2017

Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation

scientific article published on 23 October 2020

Repeating pattern of non-RVD variations in DNA-binding modules enhances TALEN activity.

scientific article

Space Radiation Biology for "Living in Space"

scientific article published on 08 April 2020

Sulforaphane suppresses metastasis of triple-negative breast cancer cells by targeting the RAF/MEK/ERK pathway

scientific article published on 24 March 2022

TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.

scientific article published on 16 December 2013

The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation.

scientific article published on 04 February 2015

Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice

scientific journal article

Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.

scientific article published on 12 January 2011

Updated summary of genome editing technology in human cultured cells linked to human genetics studies

scientific article published on 11 October 2017

YAP is essential for tissue tension to ensure vertebrate 3D body shape

scientific article

Zinc-finger nuclease-mediated targeted insertion of reporter genes for quantitative imaging of gene expression in sea urchin embryos.

scientific article

List of works by Tatsuo Miyamoto

Albatross/FBF1 contributes to both centriole duplication and centrosome separation

Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders

Characterization of Functional Primary Cilia in Human Induced Pluripotent Stem Cell-Derived Neurons

Cilia play a role in breaking left-right symmetry of the sea urchin embryo.

Ciliary GPCR-based transcriptome as a key regulator of cilia length control

Ciliopathy in PCS (MVA) syndrome.

Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential.

Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14

Cytoskeleton-related regulation of primary cilia shortening mediated by melanin-concentrating hormone receptor 1.

Efficient TALEN construction and evaluation methods for human cell and animal applications.

Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.

Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology.

Functional consequence of fibulin-4 missense mutations associated with vascular and skeletal abnormalities and cutis laxa

Generation of transgenic medaka expressing claudin7-EGFP for imaging of tight junctions in living medaka embryos.

Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer

Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.

Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome

NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations

PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation

Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation

Repeating pattern of non-RVD variations in DNA-binding modules enhances TALEN activity.

Space Radiation Biology for "Living in Space"

Sulforaphane suppresses metastasis of triple-negative breast cancer cells by targeting the RAF/MEK/ERK pathway

TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.

The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation.

Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice

Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.

Updated summary of genome editing technology in human cultured cells linked to human genetics studies

YAP is essential for tissue tension to ensure vertebrate 3D body shape

Zinc-finger nuclease-mediated targeted insertion of reporter genes for quantitative imaging of gene expression in sea urchin embryos.