about
NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domainNBS1 and its functional role in the DNA damage responseMutations of optineurin in amyotrophic lateral sclerosisObituary: a eulogy to the late Professor Tadashi Kajii (1929-2016).WRN participates in translesion synthesis pathway through interaction with NBS1Nucleolin participates in DNA double-strand break-induced damage response through MDC1-dependent pathwayZinc-finger nuclease-mediated targeted insertion of reporter genes for quantitative imaging of gene expression in sea urchin embryos.YAP is essential for tissue tension to ensure vertebrate 3D body shapeRepeating pattern of non-RVD variations in DNA-binding modules enhances TALEN activity.The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation.TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome.NBS1 recruits RAD18 via a RAD6-like domain and regulates Pol η-dependent translesion DNA synthesis.Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates.Chromosomal instability syndrome of total premature chromatid separation with mosaic variegated aneuploidy is defective in mitotic-spindle checkpoint.BubR1 localizes to centrosomes and suppresses centrosome amplification via regulating Plk1 activity in interphase cells.Expression of full-length NBS1 protein restores normal radiation responses in cells from Nijmegen breakage syndrome patients.Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation.Combined immunodeficiency, chromosomal instability, and postnatal growth deficiency in a Japanese girl.Two unrelated patients with MRE11A mutations and Nijmegen breakage syndrome-like severe microcephaly.Ciliopathy in PCS (MVA) syndrome.Exome sequencing reveals a novel MRE11 mutation in a patient with progressive myoclonic ataxia.Absence of Ku70 gene obliterates X-ray-induced lacZ mutagenesis of small deletions in mouse tissues.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.Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease?Wilms tumor accompanied by premature chromatid separation.NBS1 prevents chromatid-type aberrations through ATM-dependent interactions with SMC1.TopBP1 associates with NBS1 and is involved in homologous recombination repair.Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.Homologous recombination repair is regulated by domains at the N- and C-terminus of NBS1 and is dissociated with ATM functionsA polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locusSporadic neonatal Fanconi's anemia with VACTERL associationInsufficiency of ciliary cholesterol in hereditary Zellweger syndrome
P50
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P50
description
researcher ORCID ID = 0000-0001-5294-081X
@en
wetenschapper
@nl
name
Shinya Matsuura
@ast
Shinya Matsuura
@en
Shinya Matsuura
@es
Shinya Matsuura
@nl
type
label
Shinya Matsuura
@ast
Shinya Matsuura
@en
Shinya Matsuura
@es
Shinya Matsuura
@nl
prefLabel
Shinya Matsuura
@ast
Shinya Matsuura
@en
Shinya Matsuura
@es
Shinya Matsuura
@nl
P31
P496
0000-0001-5294-081X