Year |
Citation |
Score |
2013 |
Han H, Irimia M, Ross PJ, Sung HK, Alipanahi B, David L, Golipour A, Gabut M, Michael IP, Nachman EN, Wang E, Trcka D, Thompson T, O'Hanlon D, Slobodeniuc V, et al. MBNL proteins repress ES-cell-specific alternative splicing and reprogramming. Nature. 498: 241-5. PMID 23739326 DOI: 10.1038/nature12270 |
0.48 |
|
2012 |
Golipour A, David L, Liu Y, Jayakumaran G, Hirsch CL, Trcka D, Wrana JL. A late transition in somatic cell reprogramming requires regulators distinct from the pluripotency network. Cell Stem Cell. 11: 769-82. PMID 23217423 DOI: 10.1016/j.stem.2012.11.008 |
0.48 |
|
2011 |
David L, Samavarchi-Tehrani P, Golipour A, Wrana JL. Looking into the black box: insights into the mechanisms of somatic cell reprogramming. Genes. 2: 81-106. PMID 24710139 DOI: 10.3390/genes2010081 |
0.48 |
|
2010 |
Samavarchi-Tehrani P, Golipour A, David L, Sung HK, Beyer TA, Datti A, Woltjen K, Nagy A, Wrana JL. Functional genomics reveals a BMP-driven mesenchymal-to-epithelial transition in the initiation of somatic cell reprogramming. Cell Stem Cell. 7: 64-77. PMID 20621051 DOI: 10.1016/j.stem.2010.04.015 |
0.48 |
|
Low-probability matches |
2008 |
Golipour A, Myers D, Seagroves T, Murphy D, Evan GI, Donoghue DJ, Moorehead RA, Porter LA. The Spy1/RINGO family represents a novel mechanism regulating mammary growth and tumorigenesis. Cancer Research. 68: 3591-600. PMID 18483240 DOI: 10.1158/0008-5472.CAN-07-6453 |
0.28 |
|
2021 |
Dahl M, Smith EMK, Warsi S, Rothe M, Ferraz MJ, Aerts JMFG, Golipour A, Harper C, Pfeifer R, Pizzurro D, Schambach A, Mason C, Karlsson S. Correction of pathology in mice displaying Gaucher disease type 1 by a clinically-applicable lentiviral vector. Molecular Therapy. Methods & Clinical Development. 20: 312-323. PMID 33511245 DOI: 10.1016/j.omtm.2020.11.018 |
0.01 |
|
2020 |
Volck B, Fallet S, Thomas M, Carnley B, Golipour A, Phillips D, Mason C. AVR-RD-01 lentiviral gene therapy reduces Gb3 substrate in endothelial cells of renal peritubular capillaries in a previously untreated classic Fabry disease male patient Molecular Genetics and Metabolism. 129: S156-S157. DOI: 10.1016/j.ymgme.2019.11.416 |
0.01 |
|
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