ZINC REQUIREMENT FOR DNA REPLICATION IN STIMULATED HUMAN LYMPHOCYTES

por Williams, Richard O., Loeb, Lawrence A.
Publicado 1973

Accurate RNA consensus sequencing for high-fidelity detection of transcriptional mutagenesis-induced epimutations

por Reid-Bayliss, Kate S., Loeb, Lawrence A.
Publicado 2017

Rare Mutations in Cancer Drug Resistance and Implications for Therapy

por Beckman, Robert A., Loeb, Lawrence A.
Publicado 2020

The Werner Syndrome Protein Is Distinguished from the Bloom Syndrome Protein by Its Capacity to Tightly Bind Diverse DNA Structures

por Kamath-Loeb, Ashwini, Loeb, Lawrence A., Fry, Michael
Publicado 2012

Exploring the implications of distinct mutational signatures and mutation rates in aging and cancer

por Fox, Edward J., Salk, Jesse J., Loeb, Lawrence A.
Publicado 2016

AUSTRALIA ANTIGEN (A HEPATITIS-ASSOCIATED ANTIGEN) : PURIFICATION AND PHYSICAL PROPERTIES

por Millman, Irving, Loeb, Lawrence A., Bayer, Manfred E., Blumberg, Baruch S.
Publicado 1970

Ultra-Sensitive Sequencing Reveals an Age-Related Increase in Somatic Mitochondrial Mutations That Are Inconsistent with Oxidative Damage

por Kennedy, Scott R., Salk, Jesse J., Schmitt, Michael W., Loeb, Lawrence A.
Publicado 2013

A Rapid Assay for Measuring Nucleotide Excision Repair by Oligonucleotide Retrieval

por Shen, Jiang-Cheng, Fox, Edward J., Ahn, Eun Hyun, Loeb, Lawrence A.
Publicado 2014

Detection of Ultra-Rare Mitochondrial Mutations in Breast Stem Cells by Duplex Sequencing

por Ahn, Eun Hyun, Hirohata, Kensen, Kohrn, Brendan F., Fox, Edward J., Chang, Chia-Cheng, Loeb, Lawrence A.
Publicado 2015

A random mutation capture assay to detect genomic point mutations in mouse tissue

por Wright, Jocelyn H., Modjeski, Kristina L., Bielas, Jason H., Preston, Bradley D., Fausto, Nelson, Loeb, Lawrence A., Campbell, Jean S.
Publicado 2011

Mutations based on viral decay acceleration in the HIV-1 genomes of a clinical population treated with the mutagenic nucleoside KP1461

por Mullins, James I, Heath, Laura, Hughes, James P, Li, Deyu, Essigmann, John M, Harris, Kevin S, Simpson, Jeffrey H, Laurent, Jean-Pierre, Loeb, Lawrence A, Parkins, Jeff
Publicado 2011

Extensive subclonal mutational diversity in human colorectal cancer and its significance

por Loeb, Lawrence A., Kohrn, Brendan F., Loubet-Senear, Kaitlyn J., Dunn, Yasmin J., Ahn, Eun Hyun, O’Sullivan, Jacintha N., Salk, Jesse J., Bronner, Mary P., Beckman, Robert A.
Publicado 2019

Roles of DNA polymerase I in leading and lagging-strand replication defined by a high-resolution mutation footprint of ColE1 plasmid replication

por Allen, Jennifer M., Simcha, David M., Ericson, Nolan G., Alexander, David L., Marquette, Jacob T., Van Biber, Benjamin P., Troll, Chris J., Karchin, Rachel, Bielas, Jason H., Loeb, Lawrence A., Camps, Manel
Publicado 2011

Mutation of HIV-1 Genomes in a Clinical Population Treated with the Mutagenic Nucleoside KP1461

por Mullins, James I., Heath, Laura, Hughes, James P., Kicha, Jessica, Styrchak, Sheila, Wong, Kim G., Rao, Ushnal, Hansen, Alexis, Harris, Kevin S., Laurent, Jean-Pierre, Li, Deyu, Simpson, Jeffrey H., Essigmann, John M., Loeb, Lawrence A., Parkins, Jeffrey
Publicado 2011

Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype

por Kamath-Loeb, Ashwini S., Zavala-van Rankin, Diego G., Flores-Morales, Jeny, Emond, Mary J., Sidorova, Julia M., Carnevale, Alessandra, Cárdenas-Cortés, Maria del Carmen, Norwood, Thomas H., Monnat, Raymond J., Loeb, Lawrence A., Mercado-Celis, Gabriela E.
Publicado 2017

An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy

por Weedon, Michael N., Ellard, Sian, Prindle, Marc J., Caswell, Richard, Allen, Hana Lango, Oram, Richard, Godbole, Koumudi, Yajnik, Chittaranjan S., Sbraccia, Paolo, Novelli, Giuseppe, Turnpenny, Peter, McCann, Emma, Goh, Kim Jee, Wang, Yukai, Fulford, Jonathan, McCulloch, Laura J., Savage, David B., O’Rahilly, Stephen, Kos, Katarina, Loeb, Lawrence A., Semple, Robert K., Hattersley, Andrew T.
Publicado 2013