Agata M. Smogorzewska, Ph.D. - Publications

Affiliations: 
2009- Rockefeller University, New York, NY, United States 
Area:
Genome Maintenance
Website:
https://www.rockefeller.edu/our-scientists/heads-of-laboratories/976-agata-smogorzewska/

30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Mazzucco AE, Smogorzewska A, Kang C, Luo J, Schlabach MR, Xu Q, Patel R, Elledge SJ. Corrigendum: Genetic interrogation of replicative senescence uncovers a dual role for USP28 in coordinating the p53 and GATA4 branches of the senescence program. Genes & Development. 31: 2310. PMID 29284711 DOI: 10.1101/gad.309864.117  1
2017 Mazzucco AE, Smogorzewska A, Kang C, Luo J, Schlabach MR, Xu Q, Patel R, Elledge SJ. Genetic interrogation of replicative senescence uncovers a dual role for USP28 in coordinating the p53 and GATA4 branches of the senescence program. Genes & Development. 31: 1933-1938. PMID 29089421 DOI: 10.1101/gad.304857.117  1
2015 Kutler DI, Patel KR, Auerbach AD, Kennedy J, Lach FP, Sanborn E, Cohen MA, Kuhel WI, Smogorzewska A. Natural history and management of Fanconi anemia patients with head and neck cancer: A 10 year follow-up. The Laryngoscope. PMID 26484938 DOI: 10.1002/lary.25726  1
2015 Rickman KA, Lach FP, Abhyankar A, Donovan FX, Sanborn EM, Kennedy JA, Sougnez C, Gabriel SB, Elemento O, Chandrasekharappa SC, Schindler D, Auerbach AD, Smogorzewska A. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia. Cell Reports. PMID 26119737 DOI: 10.1016/j.celrep.2015.06.014  1
2015 Ouyang J, Garner E, Hallet A, Nguyen HD, Rickman KA, Gill G, Smogorzewska A, Zou L. Noncovalent interactions with SUMO and ubiquitin orchestrate distinct functions of the SLX4 complex in genome maintenance. Molecular Cell. 57: 108-22. PMID 25533185 DOI: 10.1016/j.molcel.2014.11.015  1
2014 Wang R, Persky NS, Yoo B, Ouerfelli O, Smogorzewska A, Elledge SJ, Pavletich NP. DNA repair. Mechanism of DNA interstrand cross-link processing by repair nuclease FAN1. Science (New York, N.Y.). 346: 1127-30. PMID 25430771 DOI: 10.1126/science.1258973  1
2013 Chandrasekharappa SC, Lach FP, Kimble DC, Kamat A, Teer JK, Donovan FX, Flynn E, Sen SK, Thongthip S, Sanborn E, Smogorzewska A, Auerbach AD, Ostrander EA. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia. Blood. 121: e138-48. PMID 23613520 DOI: 10.1182/blood-2012-12-474585  1
2013 Kim Y, Spitz GS, Veturi U, Lach FP, Auerbach AD, Smogorzewska A. Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4. Blood. 121: 54-63. PMID 23093618 DOI: 10.1182/blood-2012-07-441212  1
2012 Adamson B, Smogorzewska A, Sigoillot FD, King RW, Elledge SJ. A genome-wide homologous recombination screen identifies the RNA-binding protein RBMX as a component of the DNA-damage response. Nature Cell Biology. 14: 318-28. PMID 22344029 DOI: 10.1038/ncb2426  1
2011 Joo W, Xu G, Persky NS, Smogorzewska A, Rudge DG, Buzovetsky O, Elledge SJ, Pavletich NP. Structure of the FANCI-FANCD2 complex: Insights into the Fanconi anemia DNA repair pathway Science. 333: 312-316. PMID 21764741 DOI: 10.1126/science.1205805  1
2011 Garner E, Smogorzewska A. Ubiquitylation and the Fanconi anemia pathway Febs Letters. 585: 2853-2860. PMID 21605559 DOI: 10.1016/j.febslet.2011.04.078  1
2011 Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A. Mutations of the SLX4 gene in Fanconi anemia. Nature Genetics. 43: 142-6. PMID 21240275 DOI: 10.1038/ng.750  1
2010 Burrows AE, Smogorzewska A, Elledge SJ. Polybromo-associated BRG1-associated factor components BRD7 and BAF180 are critical regulators of p53 required for induction of replicative senescence Proceedings of the National Academy of Sciences of the United States of America. 107: 14280-14285. PMID 20660729 DOI: 10.1073/pnas.1009559107  1
2010 Smogorzewska A, Desetty R, Saito TT, Schlabach M, Lach FP, Sowa ME, Clark AB, Kunkel TA, Harper JW, Colaiácovo MP, Elledge SJ. A Genetic Screen Identifies FAN1, a Fanconi Anemia-Associated Nuclease Necessary for DNA Interstrand Crosslink Repair Molecular Cell. 39: 36-47. PMID 20603073 DOI: 10.1016/j.molcel.2010.06.023  1
2009 Knipscheer P, Räschle M, Smogorzewska A, Enoiu M, Ho TV, Schärer OD, Elledge SJ, Walter JC. The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair. Science (New York, N.Y.). 326: 1698-701. PMID 19965384 DOI: 10.1126/science.1182372  1
2009 Svendsen JM, Smogorzewska A, Sowa ME, O'Connell BC, Gygi SP, Elledge SJ, Harper JW. Mammalian BTBD12/SLX4 Assembles A Holliday Junction Resolvase and Is Required for DNA Repair Cell. 138: 63-77. PMID 19596235 DOI: 10.1016/j.cell.2009.06.030  1
2008 Ishiai M, Kitao H, Smogorzewska A, Tomida J, Kinomura A, Uchida E, Saberi A, Kinoshita E, Kinoshita-Kikuta E, Koike T, Tashiro S, Elledge SJ, Takata M. FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway Nature Structural and Molecular Biology. 15: 1138-1146. PMID 18931676 DOI: 10.1038/nsmb.1504  1
2008 Schlabach MR, Luo J, Solimini NL, Hu G, Xu Q, Li MZ, Zhao Z, Smogorzewska A, Sowa ME, Ang XL, Westbrook TF, Liang AC, Chang K, Hackett JA, Harper JW, et al. Cancer proliferation gene discovery through functional genomics Science. 319: 620-624. PMID 18239126 DOI: 10.1126/science.1149200  1
2007 Wang B, Matsuoka S, Ballif BA, Zhang D, Smogorzewska A, Gygi SP, Elledge SJ. Abraxas and RAP80 form a BRCA1 protein complex required for the DNA damage response Science. 316: 1194-1198. PMID 17525340 DOI: 10.1126/science.1139476  1
2007 Matsuoka S, Ballif BA, Smogorzewska A, McDonald ER, Hurov KE, Luo J, Bakalarski CE, Zhao Z, Solimini N, Lerenthal Y, Shiloh Y, Gygi SP, Elledge SJ. ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage Science. 316: 1160-1166. PMID 17525332 DOI: 10.1126/science.1140321  1
2007 Smogorzewska A, Matsuoka S, Vinciguerra P, McDonald ER, Hurov KE, Luo J, Ballif BA, Gygi SP, Hofmann K, D'Andrea AD, Elledge SJ. Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair. Cell. 129: 289-301. PMID 17412408 DOI: 10.1016/j.cell.2007.03.009  1
2004 Wang RC, Smogorzewska A, de Lange T. Homologous recombination generates T-loop-sized deletions at human telomeres. Cell. 119: 355-68. PMID 15507207 DOI: 10.1016/j.cell.2004.10.011  1
2004 Smogorzewska A, de Lange T. Regulation of telomerase by telomeric proteins. Annual Review of Biochemistry. 73: 177-208. PMID 15189140 DOI: 10.1146/annurev.biochem.73.071403.160049  1
2003 Takai H, Smogorzewska A, de Lange T. DNA damage foci at dysfunctional telomeres. Current Biology : Cb. 13: 1549-56. PMID 12956959 DOI: 10.1016/S0960-9822(03)00542-6  1
2002 Smogorzewska A, Karlseder J, Holtgreve-Grez H, Jauch A, de Lange T. DNA ligase IV-dependent NHEJ of deprotected mammalian telomeres in G1 and G2. Current Biology : Cb. 12: 1635-44. PMID 12361565 DOI: 10.1016/S0960-9822(02)01179-X  1
2002 Smogorzewska A, de Lange T. Different telomere damage signaling pathways in human and mouse cells. The Embo Journal. 21: 4338-48. PMID 12169636 DOI: 10.1093/emboj/cdf433  1
2002 Karlseder J, Smogorzewska A, de Lange T. Senescence induced by altered telomere state, not telomere loss. Science (New York, N.Y.). 295: 2446-9. PMID 11923537 DOI: 10.1126/science.1069523  1
2000 Smogorzewska A, Van Steensel B, Bianchi A, Oelmann S, Schaefer MR, Schnapp G, De Lange T. Control of human telomere length by TRF1 and TRF2 Molecular and Cellular Biology. 20: 1659-1668. PMID 10669743 DOI: 10.1128/MCB.20.5.1659-1668.2000  1
1998 Van Steensel B, Smogorzewska A, De Lange T. TRF2 protects human telomeres from end-to-end fusions Cell. 92: 401-413. PMID 9476899 DOI: 10.1016/S0092-8674(00)80932-0  1
1997 Broccoli D, Smogorzewska A, Chong L, de Lange T. Human telomeres contain two distinct Myb-related proteins, TRF1 and TRF2. Nature Genetics. 17: 231-5. PMID 9326950 DOI: 10.1038/ng1097-231  1
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