研究成果(長尾恒治)
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007
"Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency."
Sci Rep 2020 10:10985.
プレスリリース 先天性下垂体機能低下症の症例で新たな遺伝子変異を同定 -
006
"Asymmetrical localization of Nup107-160 subcomplex components within the nuclear pore complex in fission yeast."
PLoS Genet 2019 15: e1008061.
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005
"Genome-wide stability of the DNA replication program in single mammalian cells."
Nat Genet 2019 51: 529–540.
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004
"Role of SmcHD1 in establishment of epigenetic states required for the maintenance of the X-inactivated state in mice."
Development 2018 145: dev166462.
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003
"Nucleosomes around a mismatched base pair are excluded via an Msh2-dependent reaction with the aid of SNF2 family ATPase Smarcad1."
Genes Dev 2018 32: 806–821.
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002
"Defects in dosage compensation impact global gene regulation in the mouse trophoblast."
Development 2017 144: 2784–2797.
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001
"Inhibition of RIF1 by SCAI allows BRCA1-mediated repair."
Cell Rep 2017 20: 297–307.