Michael Lovett - Publications

Affiliations: 
Biology & Biomedical Sciences (Molecular Genetics & Genomics) Washington University, Saint Louis, St. Louis, MO 
Area:
Genetics, Evolution and Development Biology

73 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
2020 Keder A, Tardieu C, Malong L, Filia A, Kashkenbayeva A, Newton F, Georgiades M, Gale JE, Lovett M, Jarman AP, Albert JT. Homeostatic maintenance and age-related functional decline in the Drosophila ear. Scientific Reports. 10: 7431. PMID 32366993 DOI: 10.1038/S41598-020-64498-Z  0.388
2019 Wan L, Lovett M, Warchol ME, Stone JS. Vascular endothelial growth factor is required for regeneration of auditory hair cells in the avian inner ear. Hearing Research. 385: 107839. PMID 31760261 DOI: 10.1016/J.Heares.2019.107839  0.389
2018 Taylor RR, Filia A, Paredes U, Asai Y, Holt JR, Lovett M, Forge A. Regenerating hair cells in human vestibular sensory epithelia. Elife. 7. PMID 30019672 DOI: 10.7554/Elife.34817  0.463
2018 Taylor RR, Filia A, Paredes U, Asai Y, Holt JR, Lovett M, Forge A. Author response: Regenerating hair cells in vestibular sensory epithelia from humans Elife. DOI: 10.7554/Elife.34817.016  0.33
2017 Warchol ME, Stone J, Barton M, Ku J, Veile R, Daudet N, Lovett M. ADAM10 and γ-Secretase Regulate Sensory Regeneration in the Avian Vestibular Organs. Developmental Biology. PMID 28526588 DOI: 10.1016/J.Ydbio.2017.05.014  0.443
2017 Forge A, Taylor RR, Dawson SJ, Lovett M, Jagger DJ. Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear. Plos Genetics. 13: e1006692. PMID 28346477 DOI: 10.1371/Journal.Pgen.1006692  0.434
2014 Thiede BR, Mann ZF, Chang W, Ku YC, Son YK, Lovett M, Kelley MW, Corwin JT. Retinoic acid signalling regulates the development of tonotopically patterned hair cells in the chicken cochlea. Nature Communications. 5: 3840. PMID 24845860 DOI: 10.1038/Ncomms4840  0.641
2014 Mann ZF, Thiede BR, Chang W, Shin JB, May-Simera HL, Lovett M, Corwin JT, Kelley MW. A gradient of Bmp7 specifies the tonotopic axis in the developing inner ear. Nature Communications. 5: 3839. PMID 24845721 DOI: 10.1038/Ncomms4839  0.357
2014 Alvarado DM, Yang P, Druley TE, Lovett M, Gurnett CA. Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection. Nucleic Acids Research. 42: e82. PMID 24682816 DOI: 10.1093/Nar/Gku218  0.63
2014 Ku YC, Renaud NA, Veile RA, Helms C, Voelker CC, Warchol ME, Lovett M. The transcriptome of utricle hair cell regeneration in the avian inner ear. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 3523-35. PMID 24599453 DOI: 10.1523/Jneurosci.2606-13.2014  0.709
2013 Lovett M. The applications of single-cell genomics. Human Molecular Genetics. 22: R22-6. PMID 23922233 DOI: 10.1093/Hmg/Ddt377  0.332
2012 Yang KC, Ku YC, Lovett M, Nerbonne JM. Combined deep microRNA and mRNA sequencing identifies protective transcriptomal signature of enhanced PI3Kα signaling in cardiac hypertrophy. Journal of Molecular and Cellular Cardiology. 53: 101-12. PMID 22580345 DOI: 10.1016/J.Yjmcc.2012.04.012  0.605
2012 Powder KE, Ku YC, Brugmann SA, Veile RA, Renaud NA, Helms JA, Lovett M. A cross-species analysis of microRNAs in the developing avian face. Plos One. 7: e35111. PMID 22523571 DOI: 10.1371/Journal.Pone.0035111  0.746
2011 Alvarado DM, Hawkins RD, Bashiardes S, Veile RA, Ku YC, Powder KE, Spriggs MK, Speck JD, Warchol ME, Lovett M. An RNA interference-based screen of transcription factor genes identifies pathways necessary for sensory regeneration in the avian inner ear. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 4535-43. PMID 21430154 DOI: 10.1523/Jneurosci.5456-10.2011  0.763
2011 Sajan SA, Rubenstein JL, Warchol ME, Lovett M. Identification of direct downstream targets of Dlx5 during early inner ear development. Human Molecular Genetics. 20: 1262-73. PMID 21227998 DOI: 10.1093/Hmg/Ddq567  0.786
2010 Brugmann SA, Powder KE, Young NM, Goodnough LH, Hahn SM, James AW, Helms JA, Lovett M. Comparative gene expression analysis of avian embryonic facial structures reveals new candidates for human craniofacial disorders. Human Molecular Genetics. 19: 920-30. PMID 20015954 DOI: 10.1093/Hmg/Ddp559  0.789
2009 Alvarado DM, Veile R, Speck J, Warchol M, Lovett M. Downstream targets of GATA3 in the vestibular sensory organs of the inner ear. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 238: 3093-102. PMID 19924793 DOI: 10.1002/Dvdy.22149  0.726
2007 Sajan SA, Warchol ME, Lovett M. Toward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysis. Genetics. 177: 631-53. PMID 17660535 DOI: 10.1534/Genetics.107.078584  0.784
2007 Hawkins RD, Bashiardes S, Powder KE, Sajan SA, Bhonagiri V, Alvarado DM, Speck J, Warchol ME, Lovett M. Large scale gene expression profiles of regenerating inner ear sensory epithelia. Plos One. 2: e525. PMID 17565378 DOI: 10.1371/Journal.Pone.0000525  0.747
2007 Shi M, Christensen K, Weinberg CR, Romitti P, Bathum L, Lozada A, Morris RW, Lovett M, Murray JC. Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants. American Journal of Human Genetics. 80: 76-90. PMID 17160896 DOI: 10.1086/510518  0.377
2006 Ingraham CR, Kinoshita A, Kondo S, Yang B, Sajan S, Trout KJ, Malik MI, Dunnwald M, Goudy SL, Lovett M, Murray JC, Schutte BC. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nature Genetics. 38: 1335-40. PMID 17041601 DOI: 10.1038/Ng1903  0.732
2006 Hawkins RD, Helms CA, Winston JB, Warchol ME, Lovett M. Applying genomics to the avian inner ear: development of subtractive cDNA resources for exploring sensory function and hair cell regeneration. Genomics. 87: 801-8. PMID 16516437 DOI: 10.1016/J.Ygeno.2005.12.014  0.507
2006 Giannakis M, Stappenbeck TS, Mills JC, Leip DG, Lovett M, Clifton SW, Ippolito JE, Glasscock JI, Arumugam M, Brent MR, Gordon JI. Molecular properties of adult mouse gastric and intestinal epithelial progenitors in their niches. The Journal of Biological Chemistry. 281: 11292-300. PMID 16464855 DOI: 10.1074/Jbc.M512118200  0.399
2006 Park JW, Cai J, McIntosh I, Jabs EW, Fallin MD, Ingersoll R, Hetmanski JB, Vekemans M, Attie-Bitach T, Lovett M, Scott AF, Beaty TH. High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts. Journal of Medical Genetics. 43: 598-608. PMID 16415175 DOI: 10.1136/Jmg.2005.040162  0.396
2005 Cai J, Ash D, Kotch LE, Jabs EW, Attie-Bitach T, Auge J, Mattei G, Etchevers H, Vekemans M, Korshunova Y, Tidwell R, Messina DN, Winston JB, Lovett M. Gene expression in pharyngeal arch 1 during human embryonic development. Human Molecular Genetics. 14: 903-12. PMID 15703188 DOI: 10.1093/Hmg/Ddi083  0.493
2004 Messina DN, Glasscock J, Gish W, Lovett M. An ORFeome-based analysis of human transcription factor genes and the construction of a microarray to interrogate their expression. Genome Research. 14: 2041-7. PMID 15489324 DOI: 10.1101/Gr.2584104  0.501
2004 Hawkins RD, Lovett M. The developmental genetics of auditory hair cells. Human Molecular Genetics. 13: R289-96. PMID 15358736 DOI: 10.1093/Hmg/Ddh249  0.439
2004 Bashiardes S, Veile R, Allen M, Wise CA, Dobbs M, Morcuende JA, Szappanos L, Herring JA, Bowcock AM, Lovett M. SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis. Human Genetics. 115: 81-9. PMID 15088139 DOI: 10.1007/S00439-004-1121-Y  0.431
2003 Hawkins RD, Bashiardes S, Helms CA, Hu L, Saccone NL, Warchol ME, Lovett M. Gene expression differences in quiescent versus regenerating hair cells of avian sensory epithelia: implications for human hearing and balance disorders. Human Molecular Genetics. 12: 1261-72. PMID 12761041 DOI: 10.1093/Hmg/Ddg150  0.551
2002 Bashiardes S, Veile R, Wise CA, Szappanos L, Lovett M. Positional cloning strategies for idiopathic scoliosis. Studies in Health Technology and Informatics. 91: 86-9. PMID 15457700 DOI: 10.3233/978-1-60750-935-6-86  0.303
2002 Boyadjiev SA, Chowdry AB, Shapiro RE, Paznekas WA, Wandstrat AE, Choi JW, Kasch L, Zhang G, Wollnik B, Burgess CE, Schalling M, Lovett M, Jabs EW. Physical map of the chromosome 6q22 region containing the oculodentodigital dysplasia locus: analysis of thirteen candidate genes and identification of novel ESTs and DNA polymorphisms. Cytogenetic and Genome Research. 98: 29-37. PMID 12584438 DOI: 10.1159/000068535  0.412
2002 Wise CA, Gillum JD, Seidman CE, Lindor NM, Veile R, Bashiardes S, Lovett M. Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder. Human Molecular Genetics. 11: 961-9. PMID 11971877 DOI: 10.1093/Hmg/11.8.961  0.326
2002 Appel S, Filter M, Reis A, Hennies HC, Bergheim A, Ogilvie E, Arndt S, Simmons A, Lovett M, Hide W, Ramsay M, Reichwald K, Zimmermann W, Rosenthal A. Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759. European Journal of Human Genetics : Ejhg. 10: 17-25. PMID 11896452 DOI: 10.1038/Sj.Ejhg.5200750  0.476
2001 Makrinou E, Fox M, Lovett M, Haworth K, Cameron JM, Taylor K, Edwards YH. TTY2: a multicopy Y-linked gene family. Genome Research. 11: 935-45. PMID 11381023 DOI: 10.1101/Gr.175901  0.316
2001 Bowcock AM, Lovett M. Zeroing in on tolerance. Nature Medicine. 7: 279-81. PMID 11231617 DOI: 10.1038/85408  0.379
2001 Bashiardes S, Lovett M. cDNA detection and analysis. Current Opinion in Chemical Biology. 5: 15-20. PMID 11166642 DOI: 10.1016/S1367-5931(00)00161-7  0.359
1999 Rojas K, Serrano de la Peña L, Gallardo T, Simmons A, Nyce K, McGrath R, Considine E, Vasko AJ, Peterson E, Grady D, Cox R, Andrew LJ, Lovett M, Overhauser J, Williams CJ. Physical map and characterization of transcripts in the candidate interval for familial chondrocalcinosis at chromosome 5p15.1. Genomics. 62: 177-83. PMID 10610710 DOI: 10.1006/Geno.1999.5997  0.425
1999 Simmons AD, Musy MM, Lopes CS, Hwang LY, Yang YP, Lovett M. A direct interaction between EXT proteins and glycosyltransferases is defective in hereditary multiple exostoses. Human Molecular Genetics. 8: 2155-64. PMID 10545594 DOI: 10.1093/Hmg/8.12.2155  0.391
1999 Simmons AD, Lovett M. Direct cDNA selection using large genomic DNA targets. Methods in Enzymology. 303: 111-26. PMID 10349642 DOI: 10.1016/S0076-6879(99)03010-4  0.399
1999 Queimado L, Lopes C, Du F, Martins C, Fonseca I, Bowcock AM, Soares J, Lovett M. In vitro transformation of cell lines from human salivary gland tumors. International Journal of Cancer. Journal International Du Cancer. 81: 793-8. PMID 10328235 DOI: 10.1002/(Sici)1097-0215(19990531)81:5<793::Aid-Ijc21>3.0.Co;2-4  0.303
1999 Bardien-Kruger S, Greenberg J, Tubb B, Bryan J, Queimado L, Lovett M, Ramesar RS. Refinement of the RP17 locus for autosomal dominant retinitis pigmentosa, construction of a YAC contig and investigation of the candidate gene retinal fascin. European Journal of Human Genetics : Ejhg. 7: 332-8. PMID 10234509 DOI: 10.1038/Sj.Ejhg.5200302  0.348
1998 Scott DA, Greinwald JH, Marietta JR, Drury S, Swiderski RE, Viñas A, DeAngelis MM, Carmi R, Ramesh A, Kraft ML, Elbedour K, Skworak AB, Friedman RA, Srikumari Srisailapathy CR, Verhoeven K, ... ... Lovett M, et al. Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19. Gene. 215: 461-9. PMID 9758550 DOI: 10.1016/S0378-1119(98)00316-3  0.465
1998 Greinwald JH, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ. Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31. American Journal of Medical Genetics. 78: 107-13. PMID 9674898 DOI: 10.1002/(Sici)1096-8628(19980630)78:2<107::Aid-Ajmg2>3.0.Co;2-L  0.375
1998 Simmons AD, Püschel AW, McPherson JD, Overhauser J, Lovett M. Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval. Biochemical and Biophysical Research Communications. 242: 685-91. PMID 9464278 DOI: 10.1006/Bbrc.1997.8027  0.412
1997 Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS. Novel genes mapping to the critical region of the 5q- syndrome. Genomics. 45: 88-96. PMID 9339364 DOI: 10.1006/Geno.1997.4899  0.473
1997 Guimera J, Pucharcós C, Domènech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M. Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection. Genomics. 45: 59-67. PMID 9339361 DOI: 10.1006/Geno.1997.4861  0.409
1997 Greinwald JH, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar RI, Kraft ML, Elbedour K, Yairi Y, Musy M, Skvorak AB, Van Camp G, Srisailapathy CR, Lovett M, et al. Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21. Genome Research. 7: 879-86. PMID 9314493 DOI: 10.1101/Gr.7.9.879  0.383
1997 Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ. New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71: 467-71. PMID 9286457 DOI: 10.1002/(Sici)1096-8628(19970905)71:4<467::Aid-Ajmg18>3.0.Co;2-E  0.397
1997 Gersh M, Grady D, Rojas K, Lovett M, Moyzis R, Overhauser J. Development of diagnostic tools for the analysis of 5p deletions using interphase FISH. Cytogenetics and Cell Genetics. 77: 246-51. PMID 9284926 DOI: 10.1159/000134586  0.303
1997 Zhou J, Liyanage U, Medina M, Ho C, Simmons AD, Lovett M, Kosik KS. Presenilin 1 interaction in the brain with a novel member of the Armadillo family. Neuroreport. 8: 1489-94. PMID 9172160 DOI: 10.1097/00001756-199704140-00033  0.453
1997 Clines GA, Ashley JA, Shah S, Lovett M. The structure of the human multiple exostoses 2 gene and characterization of homologs in mouse and Caenorhabditis elegans. Genome Research. 7: 359-67. PMID 9110175 DOI: 10.1101/Gr.7.4.359  0.345
1997 Wise CA, Chiang LC, Paznekas WA, Sharma M, Musy MM, Ashley JA, Lovett M, Jabs EW. TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region. Proceedings of the National Academy of Sciences of the United States of America. 94: 3110-5. PMID 9096354 DOI: 10.1073/Pnas.94.7.3110  0.345
1997 Simmons AD, Overhauser J, Lovett M. Isolation of cDNAs from the Cri-du-chat critical region by direct screening of a chromosome 5-specific cDNA library. Genome Research. 7: 118-27. PMID 9049630 DOI: 10.1101/Gr.7.2.118  0.421
1997 Wise CA, Clines GA, Massa H, Trask BJ, Lovett M. Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family. Genome Research. 7: 10-6. PMID 9037597 DOI: 10.1101/Gr.7.1.10  0.463
1996 Guimerá J, Casas C, Pucharcòs C, Solans A, Domènech A, Planas AM, Ashley J, Lovett M, Estivill X, Pritchard MA. A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region. Human Molecular Genetics. 5: 1305-10. PMID 8872470 DOI: 10.1093/Hmg/5.9.1305  0.393
1996 Stickens D, Clines G, Burbee D, Ramos P, Thomas S, Hogue D, Hecht JT, Lovett M, Evans GA. The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes. Nature Genetics. 14: 25-32. PMID 8782816 DOI: 10.1038/Ng0996-25  0.474
1996 Barbosa MD, Nguyen QA, Tchernev VT, Ashley JA, Detter JC, Blaydes SM, Brandt SJ, Chotai D, Hodgman C, Solari RC, Lovett M, Kingsmore SF. Identification of the homologous beige and Chediak-Higashi syndrome genes. Nature. 382: 262-5. PMID 8717042 DOI: 10.1038/382262A0  0.356
1995 Del Mastro RG, Wang L, Simmons AD, Gallardo TD, Clines GA, Ashley JA, Hilliard CJ, Wasmuth JJ, McPherson JD, Lovett M. Human chromosome-specific cDNA libraries: new tools for gene identification and genome annotation. Genome Research. 5: 185-94. PMID 9132272 DOI: 10.1101/Gr.5.2.185  0.429
1995 Osborne-Lawrence S, Welcsh PL, Spillman M, Chandrasekharappa SC, Gallardo TD, Lovett M, Bowcock AM. Direct selection of expressed sequences within a 1-Mb region flanking BRCA1 on human chromosome 17q21. Genomics. 25: 248-55. PMID 7774925 DOI: 10.1016/0888-7543(95)80132-6  0.501
1995 Simmons AD, Goodart SA, Gallardo TD, Overhauser J, Lovett M. Five novel genes from the cri-du-chat critical region isolated by direct selection. Human Molecular Genetics. 4: 295-302. PMID 7757083 DOI: 10.1093/Hmg/4.2.295  0.464
1994 Golub TR, Barker GF, Lovett M, Gilliland DG. Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell. 77: 307-16. PMID 8168137 DOI: 10.1016/0092-8674(94)90322-0  0.359
1994 Lovett M. Fishing for complements: finding genes by direct selection. Trends in Genetics : Tig. 10: 352-7. PMID 7985239 DOI: 10.1016/0168-9525(94)90131-7  0.423
1994 Goodart SA, Simmons AD, Grady D, Rojas K, Moyzis RK, Lovett M, Overhauser J. A yeast artificial chromosome contig of the critical region for cri-du-chat syndrome. Genomics. 24: 63-8. PMID 7896290 DOI: 10.1006/Geno.1994.1582  0.329
1993 Saltman DL, Dolganov GM, Warrington JA, Wasmuth JJ, Lovett M. A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridization. Genomics. 16: 726-32. PMID 8325647 DOI: 10.1006/Geno.1993.1254  0.331
1993 Jabs EW, Li X, Lovett M, Yamaoka LH, Taylor E, Speer MC, Coss C, Cadle R, Hall B, Brown K. Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region. Genomics. 18: 7-13. PMID 8276417 DOI: 10.1006/Geno.1993.1420  0.315
1992 Saltman DL, Dolganov GM, Pearce BS, Kuo SS, Callahan PJ, Cleary ML, Lovett M. Isolation of region-specific cosmids from chromosome 5 by hybridization with microdissection clones. Nucleic Acids Research. 20: 1401-4. PMID 1561096 DOI: 10.1093/Nar/20.6.1401  0.307
1992 Saltman DL, Dolganov GM, Hinton LM, Lovett M. Reassignment of the human macrophage colony stimulating factor gene to chromosome 1p13-21. Biochemical and Biophysical Research Communications. 182: 1139-43. PMID 1540160 DOI: 10.1016/0006-291X(92)91850-P  0.4
1992 Warrington JA, Bailey SK, Armstrong E, Aprelikova O, Alitalo K, Dolganov GM, Wilcox AS, Sikela JM, Wolfe SF, Lovett M. A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5. Genomics. 13: 803-8. PMID 1322355 DOI: 10.1016/0888-7543(92)90156-M  0.339
1991 Lovett M, Kere J, Hinton LM. Direct selection: a method for the isolation of cDNAs encoded by large genomic regions. Proceedings of the National Academy of Sciences of the United States of America. 88: 9628-32. PMID 1946378 DOI: 10.1073/Pnas.88.21.9628  0.403
1991 Warrington JA, Hall LV, Hinton LM, Miller JN, Wasmuth JJ, Lovett M. Radiation hybrid map of 13 loci on the long arm of chromosome 5. Genomics. 11: 701-8. PMID 1663488 DOI: 10.1016/0888-7543(91)90078-S  0.327
1990 Donlon TA, Krensky AM, Wallace MR, Collins FS, Lovett M, Clayberger C. Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12. Genomics. 6: 548-53. PMID 1691736 DOI: 10.1016/0888-7543(90)90485-D  0.427
1987 Lovett M, Epstein CJ. The lethal yellow allele-associated provirus results in the production of chimeric viral-host RNAs. Proceedings of the National Academy of Sciences of the United States of America. 84: 2853-7. PMID 2437585 DOI: 10.1073/Pnas.84.9.2853  0.396
1982 Clayton CE, Murphy D, Lovett M, Rigby PW. A fragment of the SV40 large T-antigen gene transforms. Nature. 299: 59-61. PMID 6287280 DOI: 10.1038/299059A0  0.309
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