| Year |
Citation |
Score |
| 2022 |
Chan YY, Ho PY, Swartzrock L, Rayburn M, Nofal R, Thongthip S, Weinberg KI, Czechowicz A. Non-Genotoxic Restoration of the Hematolymphoid System in Fanconi Anemia. Transplantation and Cellular Therapy. PMID 35995393 DOI: 10.1016/j.jtct.2022.08.015 |
0.518 |
|
| 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 |
0.657 |
|
| 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 |
0.625 |
|
| 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 |
0.588 |
|
| 2012 |
Lovejoy CA, Li W, Reisenweber S, Thongthip S, Bruno J, de Lange T, De S, Petrini JH, Sung PA, Jasin M, Rosenbluh J, Zwang Y, Weir BA, Hatton C, Ivanova E, et al. Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway. Plos Genetics. 8: e1002772. PMID 22829774 DOI: 10.1371/Journal.Pgen.1002772 |
0.593 |
|
| 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, 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 |
0.647 |
|
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