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Journal of Molecular Biology|December 13, 1996
Characterization of a mutant RecA protein that facilitates homologous genetic recombination but not recombinational DNA repair: RecA423K Ishimori, S Sommer, A Bailone, et al.
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|March 23, 2011
Making new out of old: recycling and modification of an ancient protein translocation system during eukaryotic evolution. Mechanistic comparison and phylogenetic analysis of ERAD, SELMA and the peroxisomal importomerKathrin Bolte, Nicole Gruenheit, Gregor Felsner, et al.
Human Mutation|July 29, 1999
Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2-kb region of the p53 gene reveals two common haplotypesJ Feng, C H Buzin, S H Tang, et al.
British Heart Journal|June 1, 1975
His bundle recordings in bradycardia-dependent AV block induced by premature beatsA Castellanos, S A Khuddus, L S Sommer, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996
Mutation detection by highly sensitive methods indicates that p53 gene mutations in breast cancer can have important prognostic valueJ S Kovach, A Hartmann, H Blaszyk, et al.
Cytogenetic and Genome Research|May 27, 2004
Cytogenetic damage in lymphocytes for the purpose of dose reconstruction: a review of three recent radiation accidentsA Wojcik, E Gregoire, I Hayata, et al.
Human Genetics|July 1, 1991
T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detectionR P Ketterling, C D Bottema, D D Koeberl, et al.
Mutation Research|October 23, 1997
Spontaneous mutation frequencies and spectra in p53 (+/+) and p53 (-/-) mice: a test of the 'guardian of the genome' hypothesis in the Big Blue transgenic mouse mutation detection systemV L Buettner, H Nishino, J Haavik, et al.
Clinical and Experimental Dermatology|June 26, 2003
Prediction of outcome in the treatment of onychomycosisS Sommer, R A Sheehan-Dare, M J D Goodfield, et al.
Oncogene|April 1, 2008
EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acidsZ Chen, J Feng, J-S Saldivar, et al.
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