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Jun Li et al.
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Penny A. Jeggo et al.
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James A. Maier et al.
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Safwat Abdel-Azeim et al.
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Nicolas Paquet et al.
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Haoyue Zhang et al.
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Qian Chen et al.
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Mike De Vos et al.
BIOCHEMICAL PHARMACOLOGY (2012)
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Marie-France Langelier et al.
SCIENCE (2012)
Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome
Xose S. Puente et al.
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Ruben Cabanillas et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
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Anna Vangone et al.
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Emma Bolderson et al.
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Rocio Montes de Oca et al.
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Mechanism of DNA damage induced by bromate differs from general types of oxidative stress
S Kawanishi et al.
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Structural basis for DNA bridging by barrier-to-autointegration factor
CM Bradley et al.
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Genomic instability in laminopathy-based premature aging
BH Liu et al.
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EF Pettersen et al.
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Central role for the Werner syndrome protein/poly(ADP-ribose) polymerase 1 complex in the poly(ADP-ribosyl)ation pathway after DNA damage
C von Kobbe et al.
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Barrier-to-autointegration factor: major roles in chromatin decondensation and nuclear assembly
M Segura-Totten et al.
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