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Lawrence A. Loeb

Researcher at University of Washington

Publications -  449
Citations -  41359

Lawrence A. Loeb is an academic researcher from University of Washington. The author has contributed to research in topics: DNA polymerase & DNA. The author has an hindex of 98, co-authored 447 publications receiving 39608 citations. Previous affiliations of Lawrence A. Loeb include Technion – Israel Institute of Technology & Fox Chase Cancer Center.

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8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G----T and A----C substitutions.

TL;DR: These assays illustrate mutagenic replication of oh8Gua as template causing G----T substitutions and misincorporation of Oh8G Hua as substrate causing A----C substitutions, both caused by oh8 Gua.
Journal Article

Mutator Phenotype May Be Required for Multistage Carcinogenesis

TL;DR: It is argued that an early step in tumor progression is one that induces a mutator phenotype, and an increased mutation rate in tumors could be the basis for the multiple mutations that characterize many cancers.
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Protein tolerance to random amino acid change

TL;DR: A broadly applicable approach to calculate x factors is developed and demonstrated using the human DNA repair enzyme 3-methyladenine DNA glycosylase (AAG) and the results are relevant to such diverse topics as applied molecular evolution, the rate of introduction of deleterious alleles into genomes in evolutionary history, and organisms' tolerance of mutational burden.
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Fidelity of HIV-1 reverse transcriptase

TL;DR: The high error rate of HIV-1 reverse transcriptase in vitro translates to approximately five to ten errors per HIV- 1 genome per round of replication in vivo, which suggests that misincorporation by AIDS virus is, at least in part, responsible for the hypermutability of the AIDS virus.
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Detection of ultra-rare mutations by next-generation sequencing

TL;DR: It is determined that Duplex Sequencing has a theoretical background error rate of less than one artifactual mutation per billion nucleotides sequenced and that detection of mutations present in only one of the two strands of duplex DNA can be used to identify sites of DNA damage.