Erin D. Lew, Ph.D. - Publications

Affiliations: 
Yale University, New Haven, CT 
Area:
tyrosine phosphorylation

21 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 Yokoyama Y, Lew ED, Seelige R, Tindall EA, Walsh C, Fagan PC, Lee JY, Nevarez R, Oh J, Tucker KD, Chen M, Diliberto A, Vaaler H, Smith KM, Albert A, et al. Immuno-Oncological Efficacy of RXDX-106, a Novel Small Molecule Inhibitor of the TAM (TYRO3, AXL, MER) Family of Kinases. Cancer Research. PMID 30723115 DOI: 10.1158/0008-5472.Can-18-2022  0.327
2018 Yokoyama Y, Lew ED, Walsh C, Lee J, Oh J, Tindall EA, Nevarez R, Diliberto A, Ely H, Seelige R, Albert A, Bui J, Li G. Abstract A37: Immuno-oncological efficacy of RXDX-106, a novel TAM (TYRO3, AXL, MER) family small-molecule kinase inhibitor Cancer Immunology Research. 6. DOI: 10.1158/2326-6074.Tumimm17-A37  0.322
2017 Yokoyama Y, Lew ED, Seelige R, Walsh C, Barrera M, Tindall E, Oh J, Ely H, Diliberto A, Albert A, Bui J, Li G. Abstract 4698: Immuno-oncological efficacy of RXDX-106, a novel, selective and potent small molecule TAM (TYRO3, AXL, MER) inhibitor Cancer Research. 77: 4698-4698. DOI: 10.1158/1538-7445.Am2017-4698  0.324
2017 Lew ED, Tindall EA, Oh J, Walsh C, Barrera M, Ely H, Diliberto A, Yokoyama Y, Li G, Albert A. Abstract 4191: RXDX-106, a novel, selective and potent small molecule TAM (TYRO3, AXL, MER) inhibitor, demonstrates efficacy in TAM-driven tumors Cancer Research. 77: 4191-4191. DOI: 10.1158/1538-7445.Am2017-4191  0.422
2016 Fourgeaud L, Través PG, Tufail Y, Leal-Bailey H, Lew ED, Burrola PG, Callaway P, Zagórska A, Rothlin CV, Nimmerjahn A, Lemke G. TAM receptors regulate multiple features of microglial physiology. Nature. PMID 27049947 DOI: 10.1038/Nature17630  0.378
2015 Miner JJ, Daniels BP, Shrestha B, Proenca-Modena JL, Lew ED, Lazear HM, Gorman MJ, Lemke G, Klein RS, Diamond MS. The TAM receptor Mertk protects against neuroinvasive viral infection by maintaining blood-brain barrier integrity. Nature Medicine. PMID 26523970 DOI: 10.1038/Nm.3974  0.362
2015 Dransfield I, Zagórska A, Lew ED, Michail K, Lemke G. Mer receptor tyrosine kinase mediates both tethering and phagocytosis of apoptotic cells. Cell Death & Disease. 6: e1646. PMID 25695599 DOI: 10.1038/Cddis.2015.18  0.406
2015 Lemke G, Lew ED. A ligand for ALK. Science Signaling. 8: fs2. PMID 25605971 DOI: 10.1126/Scisignal.Aaa5566  0.477
2014 Lew ED, Oh J, Burrola PG, Lax I, Zagórska A, Través PG, Schlessinger J, Lemke G. Differential TAM receptor-ligand-phospholipid interactions delimit differential TAM bioactivities. Elife. 3. PMID 25265470 DOI: 10.7554/Elife.03385  0.49
2014 Zagórska A, Través PG, Lew ED, Dransfield I, Lemke G. Diversification of TAM receptor tyrosine kinase function. Nature Immunology. 15: 920-8. PMID 25194421 DOI: 10.1038/Ni.2986  0.451
2014 Lew ED, Oh J, Burrola PG, Lax I, Zagórska A, Través PG, Schlessinger J, Lemke G. Author response: Differential TAM receptor–ligand–phospholipid interactions delimit differential TAM bioactivities Elife. DOI: 10.7554/Elife.03385.018  0.412
2013 Bhattacharyya S, Zagórska A, Lew ED, Shrestha B, Rothlin CV, Naughton J, Diamond MS, Lemke G, Young JA. Enveloped viruses disable innate immune responses in dendritic cells by direct activation of TAM receptors. Cell Host & Microbe. 14: 136-47. PMID 23954153 DOI: 10.1016/J.Chom.2013.07.005  0.405
2012 Burstyn-Cohen T, Lew ED, Través PG, Burrola PG, Hash JC, Lemke G. Genetic dissection of TAM receptor-ligand interaction in retinal pigment epithelial cell phagocytosis. Neuron. 76: 1123-32. PMID 23259948 DOI: 10.1016/J.Neuron.2012.10.015  0.381
2009 Bae JH, Lew ED, Yuzawa S, Tomé F, Lax I, Schlessinger J. The selectivity of receptor tyrosine kinase signaling is controlled by a secondary SH2 domain binding site. Cell. 138: 514-24. PMID 19665973 DOI: 10.1016/J.Cell.2009.05.028  0.534
2009 Lew ED, Furdui CM, Anderson KS, Schlessinger J. The precise sequence of FGF receptor autophosphorylation is kinetically driven and is disrupted by oncogenic mutations. Science Signaling. 2: ra6. PMID 19224897 DOI: 10.1126/Scisignal.2000021  0.58
2007 Lew ED, Bae JH, Rohmann E, Wollnik B, Schlessinger J. Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activation. Proceedings of the National Academy of Sciences of the United States of America. 104: 19802-7. PMID 18056630 DOI: 10.1073/Pnas.0709905104  0.588
2007 Shams I, Rohmann E, Eswarakumar VP, Lew ED, Yuzawa S, Wollnik B, Schlessinger J, Lax I. Lacrimo-auriculo-dento-digital syndrome is caused by reduced activity of the fibroblast growth factor 10 (FGF10)-FGF receptor 2 signaling pathway. Molecular and Cellular Biology. 27: 6903-12. PMID 17682060 DOI: 10.1128/Mcb.00544-07  0.592
2006 Eswarakumar VP, Ozcan F, Lew ED, Bae JH, Tomé F, Booth CJ, Adams DJ, Lax I, Schlessinger J. Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America. 103: 18603-8. PMID 17132737 DOI: 10.1073/Pnas.0609157103  0.552
2006 Furdui CM, Lew ED, Schlessinger J, Anderson KS. Autophosphorylation of FGFR1 kinase is mediated by a sequential and precisely ordered reaction. Molecular Cell. 21: 711-7. PMID 16507368 DOI: 10.1016/J.Molcel.2006.01.022  0.52
2006 Rohmann E, Brunner HG, Kayserili H, Uyguner O, Nürnberg G, Lew ED, Dobbie A, Eswarakumar VP, Uzumcu A, Ulubil-Emeroglu M, Leroy JG, Li Y, Becker C, Lehnerdt K, Cremers CW, et al. Mutations in different components of FGF signaling in LADD syndrome. Nature Genetics. 38: 414-7. PMID 16501574 DOI: 10.1038/Ng1757  0.546
2006 Rohmann E, Brunner HG, Kayserili H, Uyguner O, Nürnberg G, Lew ED, Dobbie A, Eswarakumar VP, Uzumcu A, Ulubil-Emeroglu M, Leroy JG, Li Y, Becker C, Lehnerdt K, Cremers CWRJ, et al. Erratum: Mutations in different components of FGF signaling in LADD syndrome Nature Genetics. 38: 495-495. DOI: 10.1038/Ng0406-495  0.493
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