| Year |
Citation |
Score |
| 2024 |
Engel JL, Zhang X, Wu M, Wang Y, Espejo Valle-Inclán J, Hu Q, Woldehawariat KS, Sanders MA, Smogorzewska A, Chen J, Cortés-Ciriano I, Lo RS, Ly P. The Fanconi anemia pathway induces chromothripsis and ecDNA-driven cancer drug resistance. Cell. PMID 39181133 DOI: 10.1016/j.cell.2024.08.001 |
0.437 |
|
| 2024 |
Conti BA, Ruiz PD, Broton C, Blobel NJ, Kottemann MC, Sridhar S, Lach FP, Wiley TF, Sasi NK, Carroll T, Smogorzewska A. RTF2 controls replication repriming and ribonucleotide excision at the replisome. Nature Communications. 15: 1943. PMID 38431617 DOI: 10.1038/s41467-024-45947-z |
0.363 |
|
| 2023 |
Ruiz PD, Smogorzewska A. Temporary HMCES-DNA cross-link prevents permanent DNA damage. Cell Reports. 43: 113594. PMID 38141170 DOI: 10.1016/j.celrep.2023.113594 |
0.39 |
|
| 2023 |
Conti BA, Ruiz PD, Broton C, Blobel NJ, Kottemann MC, Sridhar S, Lach FP, Wiley T, Sasi NK, Carroll T, Smogorzewska A. RTF2 controls replication repriming and ribonucleotide excision at the replisome. Biorxiv : the Preprint Server For Biology. PMID 36993543 DOI: 10.1101/2023.03.13.532415 |
0.374 |
|
| 2022 |
Webster ALH, Sanders MA, Patel K, Dietrich R, Noonan RJ, Lach FP, White RR, Goldfarb A, Hadi K, Edwards MM, Donovan FX, Hoogenboezem RM, Jung M, Sridhar S, Wiley TF, ... ... Smogorzewska A, et al. Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer. Nature. PMID 36450981 DOI: 10.1038/s41586-022-05253-4 |
0.344 |
|
| 2022 |
Elango R, Panday A, Lach FP, Willis NA, Nicholson K, Duffey EE, Smogorzewska A, Scully R. The structure-specific endonuclease complex SLX4-XPF regulates Tus-Ter-induced homologous recombination. Nature Structural & Molecular Biology. PMID 35941380 DOI: 10.1038/s41594-022-00812-9 |
0.406 |
|
| 2022 |
Caballero M, Ge T, Rebelo AR, Seo S, Kim S, Brooks K, Zuccaro M, Kanagaraj R, Vershkov D, Kim D, Smogorzewska A, Smolka M, Benvenisty N, West SC, Egli D, et al. Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role for MCM10 in replication timing regulation. Human Molecular Genetics. PMID 35394024 DOI: 10.1093/hmg/ddac082 |
0.362 |
|
| 2021 |
Yang Z, Wu XS, Wei Y, Polyanskaya SA, Iyer SV, Jung M, Lach FP, Adelman ER, Klingbeil O, Milazzo JP, Kramer M, Demerdash OE, Chang K, Goodwin S, Hodges E, ... ... Smogorzewska A, et al. Transcriptional silencing of ALDH2 confers a dependency on Fanconi anemia proteins in acute myeloid leukemia. Cancer Discovery. PMID 33893150 DOI: 10.1158/2159-8290.CD-20-1542 |
0.343 |
|
| 2021 |
Giunta S, Hervé S, White RR, Wilhelm T, Dumont M, Scelfo A, Gamba R, Wong CK, Rancati G, Smogorzewska A, Funabiki H, Fachinetti D. CENP-A chromatin prevents replication stress at centromeres to avoid structural aneuploidy. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 33653953 DOI: 10.1073/pnas.2015634118 |
0.333 |
|
| 2020 |
Lach FP, Singh S, Rickman KA, Ruiz PD, Noonan RJ, Hymes KB, DeLacure MD, Kennedy JA, Chandrasekharappa SC, Smogorzewska A. Esophageal Cancer as initial presentation of Fanconi anemia in patients with a hypomorphic FANCA variant. Cold Spring Harbor Molecular Case Studies. PMID 33172906 DOI: 10.1101/mcs.a005595 |
0.308 |
|
| 2020 |
Thongthip S, Conti BA, Lach FP, Smogorzewska A. Suppression of non-homologous end joining does not rescue DNA repair defects in Fanconi anemia patient cells. Cell Cycle (Georgetown, Tex.). 1-9. PMID 32865112 DOI: 10.1080/15384101.2020.1810394 |
0.791 |
|
| 2020 |
Rickman KA, Noonan RJ, Lach FP, Sridhar S, Wang AT, Abhyankar A, Huang A, Kelly M, Auerbach AD, Smogorzewska A. Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links. Genes & Development. PMID 32354836 DOI: 10.1101/Gad.336446.120 |
0.547 |
|
| 2020 |
Jung M, Ramanagoudr-Bhojappa R, van Twest S, Rosti RO, Murphy V, Tan W, Donovan FX, Lach FP, Kimble DC, Jiang C, Vaughan R, Mehta PA, Pierri F, Doufour C, Auerbach AD, ... ... Smogorzewska A, et al. Association of clinical severity with FANCB variant type in Fanconi anemia. Blood. PMID 32106311 DOI: 10.1182/Blood.2019003249 |
0.363 |
|
| 2020 |
Ardeljan D, Steranka JP, Liu C, Li Z, Taylor MS, Payer LM, Gorbounov M, Sarnecki JS, Deshpande V, Hruban RH, Boeke JD, Fenyö D, Wu PH, Smogorzewska A, Holland AJ, et al. Cell fitness screens reveal a conflict between LINE-1 retrotransposition and DNA replication. Nature Structural & Molecular Biology. 27: 168-178. PMID 32042151 DOI: 10.1038/S41594-020-0372-1 |
0.412 |
|
| 2019 |
Taylor AMR, Rothblum-Oviatt C, Ellis NA, Hickson ID, Meyer S, Crawford TO, Smogorzewska A, Pietrucha B, Weemaes C, Stewart GS. Chromosome instability syndromes. Nature Reviews. Disease Primers. 5: 64. PMID 31537806 DOI: 10.1038/s41572-019-0113-0 |
0.378 |
|
| 2019 |
Donovan FX, Solanki A, Mori M, Chavan N, George M, Kumar C S, Okuno Y, Muramastsu H, Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, ... ... Smogorzewska A, et al. A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India. Human Mutation. PMID 31513304 DOI: 10.1002/Humu.23914 |
0.367 |
|
| 2019 |
Rickman K, Smogorzewska A. Advances in understanding DNA processing and protection at stalled replication forks. The Journal of Cell Biology. 218: 1096-1107. PMID 30670471 DOI: 10.1083/Jcb.201809012 |
0.493 |
|
| 2019 |
Jung M, Sridhar S, Goldfarb A, White R, Keahi D, Noonan R, Wiley T, Lach FP, Smogorzewska A. A Novel Source of Endogenous DNA Damage That Requires Repair By the Fanconi Anemia Pathway Blood. 134: 106-106. DOI: 10.1182/Blood-2019-127686 |
0.477 |
|
| 2019 |
Smogorzewska A. Fanconi Anemia: A Paradigm for Understanding DNA Repair During Replication. Blood. 134: SCI-32-SCI-32. DOI: 10.1182/Blood-2019-121229 |
0.532 |
|
| 2018 |
Kottemann MC, Conti BA, Lach FP, Smogorzewska A. Removal of RTF2 from Stalled Replisomes Promotes Maintenance of Genome Integrity. Molecular Cell. 69: 24-35.e5. PMID 29290612 DOI: 10.1016/J.Molcel.2017.11.035 |
0.472 |
|
| 2018 |
Jung M, Ramanagoudr Bhojappa R, Rosti O, Lach FP, Donovan FX, Auerbach AD, Chandrasekharappa SC, Smogorzewska A. Clinical Severity Correlates with in Vitro Residual Function of FANCB Missense Variants Blood. 132: 2588-2588. DOI: 10.1182/Blood-2018-99-111320 |
0.346 |
|
| 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 |
0.42 |
|
| 2017 |
Asur RS, Kimble DC, Lach FP, Jung M, Donovan FX, Kamat A, Noonan RJ, Thomas JW, Park M, Chines P, Vlachos A, Auerbach AD, Smogorzewska A, Chandrasekharappa SC. Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype. Molecular Genetics & Genomic Medicine. PMID 29193904 DOI: 10.1002/Mgg3.350 |
0.308 |
|
| 2017 |
Kimble DC, Lach FP, Gregg SQ, Donovan FX, Flynn EK, Kamat A, Young A, Vemulapalli M, Thomas JW, Mullikin JC, Auerbach AD, Smogorzewska A, Chandrasekharappa SC. A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families. Human Mutation. PMID 29098742 DOI: 10.1002/Humu.23366 |
0.365 |
|
| 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 |
0.55 |
|
| 2017 |
Cottineau J, Kottemann MC, Lach FP, Kang YH, Vély F, Deenick EK, Lazarov T, Gineau L, Wang Y, Farina A, Chansel M, Lorenzo L, Piperoglou C, Ma CS, Nitschke P, ... ... Smogorzewska A, et al. Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency. The Journal of Clinical Investigation. PMID 28414293 DOI: 10.1172/Jci90727 |
0.446 |
|
| 2017 |
Lim PX, Sutherland J, Noonan R, Dananberg A, Holloman W, Smogorzewska A, Jasin M. Abstract A27: Assessing somatic tumor-associated RAD51 mutations and screening for novel dominant-interfering RAD51 proteins Molecular Cancer Research. 15. DOI: 10.1158/1557-3125.Dnarepair16-A27 |
0.481 |
|
| 2016 |
Thongthip S, Bellani M, Gregg SQ, Sridhar S, Conti BA, Chen Y, Seidman MM, Smogorzewska A. Fan1 deficiency results in DNA interstrand cross-link repair defects, enhanced tissue karyomegaly, and organ dysfunction. Genes & Development. 30: 645-59. PMID 26980189 DOI: 10.1101/Gad.276261.115 |
0.772 |
|
| 2016 |
Donovan FX, Kimble DC, Kim Y, Lach FP, Harper U, Kamat A, Jones M, Sanborn EM, Tryon R, Wagner JE, MacMillan ML, Ostrander EA, Auerbach AD, Smogorzewska A, Chandrasekharappa SC. Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia. Human Mutation. PMID 26841305 DOI: 10.1002/Humu.22962 |
0.342 |
|
| 2015 |
Wang AT, Kim T, Wagner JE, Conti BA, Lach FP, Huang AL, Molina H, Sanborn EM, Zierhut H, Cornes BK, Abhyankar A, Sougnez C, Gabriel SB, Auerbach AD, Kowalczykowski SC, ... Smogorzewska A, et al. A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination. Molecular Cell. 59: 478-90. PMID 26253028 DOI: 10.1016/J.Molcel.2015.07.009 |
0.547 |
|
| 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 |
0.404 |
|
| 2015 |
Wang AT, Smogorzewska A. SnapShot: Fanconi anemia and associated proteins. Cell. 160: 354-354.e1. PMID 25594185 DOI: 10.1016/J.Cell.2014.12.031 |
0.462 |
|
| 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 |
0.682 |
|
| 2015 |
Wang AT, Kim T, Wagner JE, Conti BA, Lach FP, Huang AL, Molina H, Sanborn EM, Zierhut H, Cornes BK, Abhyankar A, Sougnez C, Gabriel SB, Auerbach AD, Kowalczykowski SC, ... Smogorzewska A, et al. A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination Molecular Cell. 59: 478-490. DOI: 10.1016/j.molcel.2015.07.009 |
0.384 |
|
| 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 |
0.626 |
|
| 2014 |
Flynn EK, Kamat A, Lach FP, Donovan FX, Kimble DC, Narisu N, Sanborn E, Boulad F, Davies SM, Gillio AP, Harris RE, MacMillan ML, Wagner JE, Smogorzewska A, Auerbach AD, et al. Comprehensive analysis of pathogenic deletion variants in Fanconi anemia genes. Human Mutation. 35: 1342-53. PMID 25168418 DOI: 10.1002/Humu.22680 |
0.376 |
|
| 2014 |
Smogorzewska A. Abstract SY33-01: Mechanism of tumor suppression by the Fanconi anemia proteins Cancer Research. 74. DOI: 10.1158/1538-7445.Am2014-Sy33-01 |
0.552 |
|
| 2014 |
Wang R, Persky NS, Yoo B, Ouerfelli O, Smogorzewska A, Elledge SJ, Pavletich NP. Mechanism of DNA interstrand cross-link processing by repair nuclease FAN1 Science. 346: 1127-1130. DOI: 10.1126/science.1258973 |
0.541 |
|
| 2013 |
Garner E, Kim Y, Lach FP, Kottemann MC, Smogorzewska A. Human GEN1 and the SLX4-associated nucleases MUS81 and SLX1 are essential for the resolution of replication-induced Holliday junctions. Cell Reports. 5: 207-15. PMID 24080495 DOI: 10.1016/J.Celrep.2013.08.041 |
0.486 |
|
| 2013 |
Shah S, Kim Y, Ostrovnaya I, Murali R, Schrader KA, Lach FP, Sarrel K, Rau-Murthy R, Hansen N, Zhang L, Kirchhoff T, Stadler Z, Robson M, Vijai J, Offit K, ... Smogorzewska A, et al. Assessment of SLX4 Mutations in Hereditary Breast Cancers. Plos One. 8: e66961. PMID 23840564 DOI: 10.1371/Journal.Pone.0066961 |
0.434 |
|
| 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 |
0.744 |
|
| 2013 |
Kottemann MC, Smogorzewska A. Fanconi anaemia and the repair of Watson and Crick DNA crosslinks. Nature. 493: 356-63. PMID 23325218 DOI: 10.1038/Nature11863 |
0.532 |
|
| 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 |
0.51 |
|
| 2012 |
Chaki M, Airik R, Ghosh AK, Giles RH, Chen R, Slaats GG, Wang H, Hurd TW, Zhou W, Cluckey A, Gee HY, Ramaswami G, Hong CJ, Hamilton BA, Cervenka I, ... ... Smogorzewska A, et al. Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell. 150: 533-48. PMID 22863007 DOI: 10.1016/J.Cell.2012.06.028 |
0.505 |
|
| 2012 |
Zhou W, Otto EA, Cluckey A, Airik R, Hurd TW, Chaki M, Diaz K, Lach FP, Bennett GR, Gee HY, Ghosh AK, Natarajan S, Thongthip S, Veturi U, Allen SJ, ... ... Smogorzewska A, et al. FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair. Nature Genetics. 44: 910-5. PMID 22772369 DOI: 10.1038/Ng.2347 |
0.773 |
|
| 2012 |
Gineau L, Cognet C, Kara N, Lach FP, Dunne J, Veturi U, Picard C, Trouillet C, Eidenschenk C, Aoufouchi S, Alcaïs A, Smith O, Geissmann F, Feighery C, Abel L, ... Smogorzewska A, et al. Partial MCM4 deficiency in patients with growth retardation, adrenal insufficiency, and natural killer cell deficiency. The Journal of Clinical Investigation. 122: 821-32. PMID 22354167 DOI: 10.1172/Jci61014 |
0.345 |
|
| 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 |
0.644 |
|
| 2012 |
Shah S, Lach F, Kim Y, Sarrel K, Rau-Murthy R, Hansen N, Rendleman J, Kirchhoff T, Joseph V, Offit K, Smogorzewska A. Abstract 2600:SLX4mutation in hereditary breast cancer Cancer Research. 72: 2600-2600. DOI: 10.1158/1538-7445.Am2012-2600 |
0.333 |
|
| 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 |
0.607 |
|
| 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 |
0.462 |
|
| 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 |
0.494 |
|
| 2011 |
Burrows AE, Smogorzewska A, Elledge SJ. Abstract A33: A whole genome RNAi screen identifies BRD7 and BAF180 as p53 regulators required for senescence Cancer Research. 71. DOI: 10.1158/1538-7445.Fbcr11-A33 |
0.735 |
|
| 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 |
0.784 |
|
| 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 |
0.604 |
|
| 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 |
0.644 |
|
| 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 |
0.64 |
|
| 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 |
0.631 |
|
| 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 |
0.758 |
|
| 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 |
0.647 |
|
| 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 |
0.604 |
|
| 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 |
0.624 |
|
| 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 |
0.621 |
|
| 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 |
0.636 |
|
| 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 |
0.676 |
|
| 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 |
0.77 |
|
| 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 |
0.618 |
|
| 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 |
0.759 |
|
| 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 |
0.616 |
|
| 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 |
0.637 |
|
| 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 |
0.737 |
|
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