| Year |
Citation |
Score |
| 2013 |
Ray P, Viles KD, Soule EE, Woodruff RS. Application of aptamers for targeted therapeutics. Archivum Immunologiae Et Therapiae Experimentalis. 61: 255-71. PMID 23563807 DOI: 10.1007/S00005-013-0227-0 |
0.504 |
|
| 2013 |
Lawal NO, Viles KD, Barbas A, White RR. Gene and MicroRNA Profiling of Radioresistant Pancreatic Cancer Cell Lines Journal of Surgical Research. 179: 193. DOI: 10.1016/J.Jss.2012.10.216 |
0.38 |
|
| 2012 |
Rialon K, Viles K, Barbas A, Sullenger B, White R. In Vivo Selection of Aptamers Targeting Pancreatic Cancer Journal of Surgical Research. 172: 341. DOI: 10.1016/J.Jss.2011.11.709 |
0.62 |
|
| 2011 |
Barbas A, Viles K, Rialon K, Mi J, Clary B, Sullenger B, White R. In-vivo SELEX Against Pancreatic Cancer Xenografts Journal of Surgical Research. 165: 307. DOI: 10.1016/J.Jss.2010.11.362 |
0.599 |
|
| 2009 |
White R, Singh S, Hsu S, Viles K, Potti A, Nevins J, Ali-Osman F. 54: Development of a Gene Expression Profile for Predicting Gemcitabine Response in Pancreatic Cancer Journal of Surgical Research. 151: 195. DOI: 10.1016/J.Jss.2008.11.064 |
0.357 |
|
| 2008 |
White RR, Roy JA, Viles KD, Sullenger BA, Kontos CD. A nuclease-resistant RNA aptamer specifically inhibits angiopoietin-1-mediated Tie2 activation and function. Angiogenesis. 11: 395-401. PMID 19037734 DOI: 10.1007/S10456-008-9122-4 |
0.58 |
|
| 2008 |
Viles KD, Sullenger BA. Proximity-dependent and proximity-independent trans-splicing in mammalian cells. Rna (New York, N.Y.). 14: 1081-94. PMID 18441053 DOI: 10.1261/Rna.384808 |
0.579 |
|
| 2008 |
Mi J, Zhang X, Rabbani ZN, Liu Y, Reddy SK, Su Z, Salahuddin FK, Viles K, Giangrande PH, Dewhirst MW, Sullenger BA, Kontos CD, Clary BM. RNA aptamer-targeted inhibition of NF-kappa B suppresses non-small cell lung cancer resistance to doxorubicin. Molecular Therapy : the Journal of the American Society of Gene Therapy. 16: 66-73. PMID 17912235 DOI: 10.1038/Sj.Mt.6300320 |
0.609 |
|
| 2006 |
McNamara JO, Andrechek ER, Wang Y, Viles KD, Rempel RE, Gilboa E, Sullenger BA, Giangrande PH. Cell type-specific delivery of siRNAs with aptamer-siRNA chimeras. Nature Biotechnology. 24: 1005-15. PMID 16823371 DOI: 10.1038/Nbt1223 |
0.637 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2000 |
Melvin EC, George TM, Worley G, Franklin A, Mackey J, Viles K, Shah N, Drake CR, Enterline DS, McLone D, Nye J, Oakes WJ, McLaughlin C, Walker ML, Peterson P, et al. Genetic studies in neural tube defects. NTD Collaborative Group. Pediatric Neurosurgery. 32: 1-9. PMID 10765131 DOI: 10.1159/000028889 |
0.264 |
|
| 1998 |
Bartoloni L, Horrigan SK, Viles KD, Gilchrist JM, Stajich JM, Vance JM, Yamaoka LH, Pericak-Vance MA, Westbrook CA, Speer MC. Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31. Genomics. 54: 250-5. PMID 9828127 DOI: 10.1006/Geno.1998.5579 |
0.26 |
|
| 2000 |
Hauser MA, Horrigan SK, Salmikangas P, Torian UM, Viles KD, Dancel R, Tim RW, Taivainen A, Bartoloni L, Gilchrist JM, Stajich JM, Gaskell PC, Gilbert JR, Vance JM, Pericak-Vance MA, et al. Myotilin is mutated in limb girdle muscular dystrophy 1A. Human Molecular Genetics. 9: 2141-7. PMID 10958653 DOI: 10.1093/Hmg/9.14.2141 |
0.256 |
|
| 1996 |
Speer MC, Tandan R, Rao PN, Fries T, Stajich JM, Bolhuis PA, Jöbsis GJ, Vance JM, Viles KD, Sheffield K, James C, Kahler SG, Pettenati M, Gilbert JR, Denton PH, et al. Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37. Human Molecular Genetics. 5: 1043-6. PMID 8817344 DOI: 10.1093/Hmg/5.7.1043 |
0.249 |
|
| 1998 |
Pan TC, Zhang RZ, Pericak-Vance MA, Tandan R, Fries T, Stajich JM, Viles K, Vance JM, Chu ML, Speer MC. Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy. Human Molecular Genetics. 7: 807-12. PMID 9536084 DOI: 10.1093/Hmg/7.5.807 |
0.248 |
|
| 1998 |
Speer MC, Vance JM, Lennon-Graham F, Stajich JM, Viles KD, Gilchrist JM, Nigro V, McMichael R, Chutkow JG, Bartoloni L, Horrigan SK, Westbrook CA, Pericak-Vance MA. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families. Human Heredity. 48: 179-84. PMID 9694248 DOI: 10.1159/000022799 |
0.238 |
|
| 2002 |
Speer MC, Melvin EC, Viles KD, Bauer KA, Rampersaud E, Drake C, George TM, Enterline DS, Mackey JF, Worley G, Gilbert JR, Nye JS. T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families. American Journal of Medical Genetics. 110: 215-8. PMID 12116228 DOI: 10.1002/Ajmg.10436 |
0.231 |
|
| 1999 |
Speer MC, Vance JM, Grubber JM, Lennon Graham F, Stajich JM, Viles KD, Rogala A, McMichael R, Chutkow J, Goldsmith C, Tim RW, Pericak-Vance MA. Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7. American Journal of Human Genetics. 64: 556-62. PMID 9973293 DOI: 10.1086/302252 |
0.231 |
|
| 2001 |
Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy. Journal of Clinical Neuromuscular Disease. 3: 1-7. PMID 19078645 DOI: 10.1097/00131402-200109000-00001 |
0.221 |
|
| 2000 |
Nance MA, Nuttall FQ, Econs MJ, Lyles KW, Viles KD, Vance JM, Pericak-Vance MA, Speer MC. Heterogeneity in Paget disease of the bone American Journal of Medical Genetics. 92: 303-307. PMID 10861657 DOI: 10.1002/1096-8628(20000619)92:5<303::Aid-Ajmg2>3.0.Co;2-E |
0.217 |
|
| 1999 |
Speer MC, Nye J, McLone D, Worley G, Melvin EC, Viles KD, Franklin A, Drake C, Mackey J, George TM, Enterline DS, Fuchs HE, Fitch RD, Vance JM, Pericak-Vance MA, et al. Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects Clinical Genetics. 56: 142-144. PMID 10517251 DOI: 10.1034/J.1399-0004.1999.560208.X |
0.191 |
|
| 2001 |
Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, Van Der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Clinical studies in non-chromosome 4-linked facioscapulohumeral muscular dystrophy Journal of Clinical Neuromuscular Disease. 3: 1-7. |
0.115 |
|
| Hide low-probability matches. |