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Mutation spectrum of POLE and POLD1 mutations in South East Asian women presenting with grade 3 endometrioid endometrial carcinomas - ScienceDirect
Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid f
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Functional analysis of POLD1 p.ser605del variant: the aging phenotype of MDPL syndrome is associated with an impaired DNA repair capacity | Aging
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POLE/POLD1 mutation and tumor immunotherapy | Journal of Experimental & Clinical Cancer Research | Full Text
Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid f
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Candidate variants in DNA replication and repair genes in early-onset renal cell carcinoma patients referred for germline testing | BMC Genomics | Full Text
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Somatic mutations affecting MSH4, POLE and POLD1. The lollipop plots... | Download Scientific Diagram
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Top mutated DNA polymerases and mutation prevalence in Fanconi anemia... | Download Scientific Diagram
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The POLD1R689W variant increases the sensitivity of colorectal cancer cells to ATR and CHK1 inhibitors | Scientific Reports
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