Agata Smogorzewska

Agata Smogorzewska is a Polish-born scientist. She is an associate professor at Rockefeller University, heading the Laboratory of Genome Maintenance. Her work primarily focuses on DNA interstrand crosslink repair and the diseases resulting from deficiencies in this repair pathway, including Fanconi anemia and karyomegalic interstitial nephritis. Provided by Wikipedia
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  1. 1
    Temporary HMCES-DNA cross-link prevents permanent DNA damage

    Temporary HMCES-DNA cross-link prevents permanent DNA damage by Penelope D. Ruiz, Agata Smogorzewska

    Published 2024-01-01
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  2. 2
    Human GEN1 and the SLX4-Associated Nucleases MUS81 and SLX1 Are Essential for the Resolution of Replication-Induced Holliday Junctions

    Human GEN1 and the SLX4-Associated Nucleases MUS81 and SLX1 Are Essential for the Resolution of Replication-Induced Holliday Junctions by Elizabeth Garner, Yonghwan Kim, Francis P. Lach, Molly C. Kottemann, Agata Smogorzewska

    Published 2013-10-01
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  3. 3
    RTF2 controls replication repriming and ribonucleotide excision at the replisome

    RTF2 controls replication repriming and ribonucleotide excision at the replisome by Brooke A. Conti, Penelope D. Ruiz, Cayla Broton, Nicolas J. Blobel, Molly C. Kottemann, Sunandini Sridhar, Francis P. Lach, Tom F. Wiley, Nanda K. Sasi, Thomas Carroll, Agata Smogorzewska

    Published 2024-03-01
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  4. 4
    Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia

    Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia by Kimberly A. Rickman, Francis P. Lach, Avinash Abhyankar, Frank X. Donovan, Erica M. Sanborn, Jennifer A. Kennedy, Carrie Sougnez, Stacey B. Gabriel, Olivier Elemento, Settara C. Chandrasekharappa, Detlev Schindler, Arleen D. Auerbach, Agata Smogorzewska

    Published 2015-07-01
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  5. 5
    Assessment of SLX4 Mutations in Hereditary Breast Cancers.

    Assessment of SLX4 Mutations in Hereditary Breast Cancers. by Sohela Shah, Yonghwan Kim, Irina Ostrovnaya, Rajmohan Murali, Kasmintan A Schrader, Francis P Lach, Kara Sarrel, Rohini Rau-Murthy, Nichole Hansen, Liyng Zhang, Tomas Kirchhoff, Zsofia Stadler, Mark Robson, Joseph Vijai, Kenneth Offit, Agata Smogorzewska

    Published 2013-01-01
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  6. 6
    A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype

    A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype by Laura Schultz-Rogers, Francis P. Lach, Kimberly A. Rickman, Alejandro Ferrer, Abhishek A. Mangaonkar, Tanya L. Schwab, Christopher T. Schmitz, Karl J. Clark, Nikita R. Dsouza, Michael T. Zimmermann, Mark Litzow, Nicole Jacobi, Eric W. Klee, Agata Smogorzewska, Mrinal M. Patnaik

    Published 2020-07-01
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