From broken to old: DNA damage, IGF1 endocrine suppression and aging

od Monnat, Raymond J.
Izdano 2007

Human RECQ helicases: Roles in DNA metabolism, mutagenesis and cancer biology

od Monnat, Raymond J.
Izdano 2010

‘…Re-written in the skin’ – Clues to skin biology and aging from inherited disease

od Monnat, Raymond J.
Izdano u J Invest Dermatol (2015)

Letter to the Editor: Diabetes mellitus and cancer in Werner syndrome

od Lauper, Julia M., Monnat, Raymond J.
Izdano 2013

Werner Syndrome: Clinical Features, Pathogenesis and Potential Therapeutic Interventions

od Oshima, Junko, Sidorova, Julia M., Monnat, Raymond J.
Izdano u Ageing Res Rev (2016)

Loss of Werner syndrome protein function promotes aberrant mitotic recombination

od Prince, Polly R., Emond, Mary J., Monnat, Raymond J.
Izdano 2001

Comprehensive computational design of mCreI homing endonuclease cleavage specificity for genome engineering

od Ulge, Umut Y., Baker, David A., Monnat, Raymond J.
Izdano 2011

PARP-mediated Repair, Homologous Recombination, and Back-up Non-Homologous End Joining-Like Repair of Single-Strand Nicks

od Metzger, Michael J., Stoddard, Barry L., Monnat, Raymond J.
Izdano 2013

Development of a Whole Blood Paper-Based Device for Phenylalanine Detection in the Context of PKU Therapy Monitoring

od Robinson, Robert, Wong, Liam, Monnat, Raymond J., Fu, Elain
Izdano u Micromachines (Basel) (2016)

The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest

od Sidorova, Julia M., Li, Nianzhen, Folch, Albert, Monnat, Raymond J.
Izdano u Cell Cycle (2008)

Altered target site specificity variants of the I-PpoI His-Cys box homing endonuclease

od Eklund, Jennifer L., Ulge, Umut Y., Eastberg, Jennifer, Monnat, Raymond J.
Izdano 2007

Spectrum and Risk of Neoplasia in Werner Syndrome: A Systematic Review

od Lauper, Julia M., Krause, Alison, Vaughan, Thomas L., Monnat, Raymond J.
Izdano 2013

Global and disease-associated genetic variation in the human Fanconi anemia gene family

od Rogers, Kai J., Fu, Wenqing, Akey, Joshua M., Monnat, Raymond J.
Izdano u Hum Mol Genet (2014)

Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin

od Flory, Mark R., Moser, Michael J., Monnat, Raymond J., Davis, Trisha N.
Izdano 2000

Generation of single-chain LAGLIDADG homing endonucleases from native homodimeric precursor proteins

od Li, Hui, Pellenz, Stefan, Ulge, Umut, Stoddard, Barry L., Monnat, Raymond J.
Izdano 2009

Essential role for Cdk2 inhibitory phosphorylation during replication stress revealed by a human Cdk2 knockin mutation

od Hughes, Bridget T., Sidorova, Julia, Swanger, Jherek, Monnat, Raymond J., Clurman, Bruce E.
Izdano 2013

The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage

od Colgin, Lorel M., Hackmann, Alden F. M., Emond, Mary J., Monnat, Raymond J.
Izdano 2002

Microfluidic-assisted analysis of replicating DNA molecules

od Sidorova, Julia M., Li, Nianzhen, Schwartz, David C., Folch, Albert, Monnat, Raymond J.
Izdano 2009

Comprehensive homing endonuclease target site specificity profiling reveals evolutionary constraints and enables genome engineering applications

od Li, Hui, Ulge, Umut Y., Hovde, Blake T., Doyle, Lindsey A., Monnat, Raymond J.
Izdano 2012

Human RECQ Helicase Pathogenic Variants, Population Variation and “Missing” Diseases

od Fu, Wenqing, Ligabue, Alessio, Rogers, Kai J., Akey, Joshua M., Monnat, Raymond J.
Izdano u Hum Mutat (2016)