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Lifeng Xu, Ph.D. - Publications

Affiliations: 
2000 Princeton University, Princeton, NJ 
Area:
Molecular Biology, Oncology
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19 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
2019 Nera B, Huang HS, Hendrickson EA, Xu L. Both the Classical and Alternative Non-Homologous End Joining Pathways Contribute to the Fusion of Drastically Shortened Telomeres Induced by TRF2 Overexpression. Cell Cycle (Georgetown, Tex.). PMID 30907229 DOI: 10.1080/15384101.2019.1598724  0.394
2019 Sandhu R, Wei D, Sharma M, Xu L. An N-terminal Flag-tag impairs TPP1 regulation of telomerase function. Biochemical and Biophysical Research Communications. PMID 30885434 DOI: 10.1016/J.Bbrc.2019.03.050  0.342
2016 Fan Y, Wu G, Su F, Li K, Xu L, Han X, Yan Y. Lipase oriented-immobilized on dendrimer-coated magnetic multi-walled carbon nanotubes toward catalyzing biodiesel production from waste vegetable oil Fuel. 178: 172-178. DOI: 10.1016/j.fuel.2016.03.071  0.318
2015 Nera B, Huang HS, Lai T, Xu L. Elevated levels of TRF2 induce telomeric ultrafine anaphase bridges and rapid telomere deletions. Nature Communications. 6: 10132. PMID 26640040 DOI: 10.1038/Ncomms10132  0.396
2015 Frank AK, Tran DC, Qu RW, Stohr BA, Segal DJ, Xu L. The Shelterin TIN2 Subunit Mediates Recruitment of Telomerase to Telomeres. Plos Genetics. 11: e1005410. PMID 26230315 DOI: 10.1371/Journal.Pgen.1005410  0.37
2014 Tran DC, Frank AK, Xu L. Abstract 490: Investigation of telomere shortening caused by dyskeratosis congenita-associated heterozygous TIN2 mutations Cancer Research. 74: 490-490. DOI: 10.1158/1538-7445.Am2014-490  0.366
2013 Bhakta MS, Henry IM, Ousterout DG, Das KT, Lockwood SH, Meckler JF, Wallen MC, Zykovich A, Yu Y, Leo H, Xu L, Gersbach CA, Segal DJ. Highly active zinc-finger nucleases by extended modular assembly. Genome Research. 23: 530-8. PMID 23222846 DOI: 10.1101/Gr.143693.112  0.301
2013 Xu L, Li S, Stohr BA. The role of telomere biology in cancer. Annual Review of Pathology. 8: 49-78. PMID 22934675 DOI: 10.1146/Annurev-Pathol-020712-164030  0.379
2010 Stohr BA, Xu L, Blackburn EH. The terminal telomeric DNA sequence determines the mechanism of dysfunctional telomere fusion. Molecular Cell. 39: 307-14. PMID 20670897 DOI: 10.1016/J.Molcel.2010.06.020  0.378
2009 Li S, Matsuguchi T, Stohr BA, Xu L, Perry K, Ren B, Blackburn EH. Abstract IA-22: Cellular responses to telomerase perturbations Cancer Research. 69. DOI: 10.1158/0008-5472.Fbcr09-Ia-22  0.419
2009 Stohr BA, Xu L, Blackburn EH. Abstract B64: Telomeric DNA sequence determines the mechanism of dysfunctional telomere fusion in human cancer cells Cancer Research. 69. DOI: 10.1158/0008-5472.Fbcr09-B64  0.415
2008 Wang X, Kam Z, Carlton PM, Xu L, Sedat JW, Blackburn EH. Rapid telomere motions in live human cells analyzed by highly time-resolved microscopy. Epigenetics & Chromatin. 1: 4. PMID 19014413 DOI: 10.1186/1756-8935-1-4  0.334
2007 Xu L, Blackburn EH. Human cancer cells harbor T-stumps, a distinct class of extremely short telomeres. Molecular Cell. 28: 315-27. PMID 17964269 DOI: 10.1016/J.Molcel.2007.10.005  0.364
2007 Blackburn EH, Li S, Xu L. Responses of human cancer cells to telomerase interference The Faseb Journal. 21. DOI: 10.1096/Fasebj.21.5.A152-B  0.319
2004 Xu L, Blackburn EH. Human Rif1 protein binds aberrant telomeres and aligns along anaphase midzone microtubules. The Journal of Cell Biology. 167: 819-30. PMID 15583028 DOI: 10.1083/Jcb.200408181  0.392
2003 Kim M, Xu L, Blackburn EH. Catalytically active human telomerase mutants with allele-specific biological properties. Experimental Cell Research. 288: 277-87. PMID 12915119 DOI: 10.1016/S0014-4827(03)00217-9  0.353
2002 Comolli LR, Smirnov I, Xu L, Blackburn EH, James TL. A molecular switch underlies a human telomerase disease. Proceedings of the National Academy of Sciences of the United States of America. 99: 16998-7003. PMID 12482936 DOI: 10.1073/Pnas.262663599  0.318
2001 Tao W, Pennica D, Xu L, Kalejta RF, Levine AJ. Wrch-1, a novel member of the Rho gene family that is regulated by Wnt-1. Genes & Development. 15: 1796-807. PMID 11459829 DOI: 10.1101/Gad.894301  0.448
2000 Xu L, Corcoran RB, Welsh JW, Pennica D, Levine AJ. WISP-1 is a Wnt-1- and beta-catenin-responsive oncogene. Genes & Development. 14: 585-95. PMID 10716946  0.36
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