List of works - Shinya Matsuura

A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locus

scientific article published on 01 January 1999

Absence of Ku70 gene obliterates X-ray-induced lacZ mutagenesis of small deletions in mouse tissues.

scientific article published in August 2008

BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.

scientific article

Chromosomal instability syndrome of total premature chromatid separation with mosaic variegated aneuploidy is defective in mitotic-spindle checkpoint.

scientific article published on 30 June 2000

Ciliopathy in PCS (MVA) syndrome.

scientific article published on 22 August 2015

Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.

scientific article

Combined immunodeficiency, chromosomal instability, and postnatal growth deficiency in a Japanese girl.

scientific article published on April 2001

Cytoplasmic, but not nuclear, p16 expression may signal poor prognosis in high-grade astrocytomas.

scientific article

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

Exome sequencing reveals a novel MRE11 mutation in a patient with progressive myoclonic ataxia.

scientific article published in December 2013

Expression of full-length NBS1 protein restores normal radiation responses in cells from Nijmegen breakage syndrome patients.

scientific article

Homologous recombination repair is regulated by domains at the N- and C-terminus of NBS1 and is dissociated with ATM functions

scientific article published on 26 March 2007

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

Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease?

scientific article published in October 2000

Mutations of optineurin in amyotrophic lateral sclerosis

scientific article (publication date: 13 May 2010)

NBS1 and its functional role in the DNA damage response

scientific article

NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain

scientific article

NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC1.

scientific article

NBS1 recruits RAD18 via a RAD6-like domain and regulates Pol η-dependent translesion DNA synthesis.

scientific article

Nucleolin participates in DNA double-strand break-induced damage response through MDC1-dependent pathway

scientific article

Obituary: a eulogy to the late Professor Tadashi Kajii (1929-2016).

scientific article

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

scientific article published on 26 August 2017

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

scientific article

Sporadic neonatal Fanconi's anemia with VACTERL association

scientific article published on 01 February 2010

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

TopBP1 associates with NBS1 and is involved in homologous recombination repair.

scientific article published on 24 August 2007

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

scientific article published on 12 January 2011

WRN participates in translesion synthesis pathway through interaction with NBS1

scientific article

Wilms tumor accompanied by premature chromatid separation.

scientific article published on 24 September 2016

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

p16 gene transfer increases cell killing with abnormal nucleation after ionising radiation in glioma cells ⬇️

scientific article published on November 3, 2003

List of works by Shinya Matsuura

A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locus

Absence of Ku70 gene obliterates X-ray-induced lacZ mutagenesis of small deletions in mouse tissues.

BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.

Chromosomal instability syndrome of total premature chromatid separation with mosaic variegated aneuploidy is defective in mitotic-spindle checkpoint.

Ciliopathy in PCS (MVA) syndrome.

Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.

Combined immunodeficiency, chromosomal instability, and postnatal growth deficiency in a Japanese girl.

Cytoplasmic, but not nuclear, p16 expression may signal poor prognosis in high-grade astrocytomas.

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.

Exome sequencing reveals a novel MRE11 mutation in a patient with progressive myoclonic ataxia.

Expression of full-length NBS1 protein restores normal radiation responses in cells from Nijmegen breakage syndrome patients.

Homologous recombination repair is regulated by domains at the N- and C-terminus of NBS1 and is dissociated with ATM functions

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

Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome

Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease?

Mutations of optineurin in amyotrophic lateral sclerosis

NBS1 and its functional role in the DNA damage response

NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain

NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC1.

NBS1 recruits RAD18 via a RAD6-like domain and regulates Pol η-dependent translesion DNA synthesis.

Nucleolin participates in DNA double-strand break-induced damage response through MDC1-dependent pathway

Obituary: a eulogy to the late Professor Tadashi Kajii (1929-2016).

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

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

Sporadic neonatal Fanconi's anemia with VACTERL association

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.

TopBP1 associates with NBS1 and is involved in homologous recombination repair.

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

WRN participates in translesion synthesis pathway through interaction with NBS1

Wilms tumor accompanied by premature chromatid separation.

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.

p16 gene transfer increases cell killing with abnormal nucleation after ionising radiation in glioma cells ⬇️