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Kristi Viles

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Publications

TOP 3
Kristi D Viles; Bruce A Sullenger
Proximity-dependent and proximity-independent trans-splicing in mammalian cells.
Jing Mi; Xiuwu Zhang; Zahid Rabbani; Yingmiao Liu; Srinevas Reddy; Zhen Su; Fawzia K Salahuddin; Kristi D Viles; Paloma H Giangrande; Mark Dewhirst; Bruce A Sullenger; Christopher D Kontos; Bryan M Clary
RNA aptamer-targeted inhibition of NF-kappa B suppresses non-small cell lung cancer resistance to doxorubicin.
James O McNamara; Eran R Andrechek; Yong Wang; Kristi D Viles; Rachel E Rempel; Eli Gilboa; Bruce A Sullenger; Paloma H Giangrande
Cell type-specific delivery of siRNAs with aptamer-siRNA chimeras.

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All Publications

2008: Kristi D Viles; Bruce A Sullenger
Proximity-dependent and proximity-independent trans-splicing in mammalian cells.
RNA (New York, N.Y.) 2008;14(6):1081-94.
2008: Jing Mi; Xiuwu Zhang; Zahid Rabbani; Yingmiao Liu; Srinevas Reddy; Zhen Su; Fawzia K Salahuddin; Kristi D Viles; Paloma H Giangrande; Mark Dewhirst; Bruce A Sullenger; Christopher D Kontos; Bryan M Clary
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 2008;16(1):66-73.
2006: James O McNamara; Eran R Andrechek; Yong Wang; Kristi D Viles; Rachel E Rempel; Eli Gilboa; Bruce A Sullenger; Paloma H Giangrande
Cell type-specific delivery of siRNAs with aptamer-siRNA chimeras.
Nature biotechnology 2006;24(8):1005-15.
2002: Marcy C Speer; Elizabeth C Melvin; Kristi D Viles; Kim A Bauer; Evadnie Rampersaud; Courtney Drake; Timothy M George; David S Enterline; Joanne F Mackey; Gordon Worley; John Gilbert; Jeffrey S Nye
T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families.
American journal of medical genetics 2002;110(3):215-8.
2001: RW Tim; Silvère M van der Maarel; Kristi D Viles; Jeffrey M Stajich; R Tawil; E H Bossen; Rune R Frants; A H Friedman; John Gilbert; George W Padberg; Margaret Pericak-Vance; Evadnie Rampersaud; Marcy C Speer
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy.
Journal of clinical neuromuscular disease 2001;3(1):1-7.
2000: Michael A Hauser; stephen horrigan; Paula Salmikangas; U M Torian; Kristi D Viles; R Dancel; RW Tim; Anu Taivainen; L Bartoloni; JM Gilchrist; Jeffrey M Stajich; Perry C Gaskell; John Gilbert; Jeffery Vance; Margaret Pericak-Vance; Olli Carpen; Carol A Westbrook; Marcy C Speer
Myotilin is mutated in limb girdle muscular dystrophy 1A.
Human molecular genetics 2000;9(14):2141-7.
2000: Martha A Nance; F Q Nuttall; Michael J Econs; K W Lyles; Kristi D Viles; Jeffery Vance; Margaret Pericak-Vance; Marcy C Speer
Heterogeneity in Paget disease of the bone.
American journal of medical genetics 2000;92(5):303-7.
2000: Elizabeth C Melvin; Timothy M George; Gordon Worley; A Franklin; Joanne Mackey; Kristi D Viles; N Shah; C R Drake; David S Enterline; D McLone; Jeffrey S Nye; W J Oakes; Colleen McLaughlin; M L Walker; P Peterson; Timothy J Brei; C Buran; J Aben; B Ohm; I Bermans; Mazin B Qumsiyeh; Jeffery Vance; Margaret Pericak-Vance; Marcy C Speer
Genetic studies in neural tube defects. NTD Collaborative Group.
Pediatric neurosurgery 2000;32(1):1-9.
1999: Marcy C Speer; Jeffrey S Nye; D McLone; Gordon Worley; Elizabeth C Melvin; Kristi D Viles; A Franklin; C Drake; Joanne Mackey; Timothy M George
Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group.
Clinical genetics 1999;56(2):142-4.
1999: Marcy C Speer; Jeffery Vance; Janet Grubber; F Lennon Graham; Jeffrey M Stajich; Kristi D Viles; AR Rogala; R McMichael; J Chutkow; C Goldsmith; RW Tim; Margaret Pericak-Vance
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.
American journal of human genetics 1999;64(2):556-62.
1998: L Bartoloni; stephen horrigan; Kristi D Viles; JM Gilchrist; Jeffrey M Stajich; Jeffery Vance; LH Yamaoka; Margaret Pericak-Vance; Carol A Westbrook; Marcy C Speer
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 1998;54(2):250-5.
1998: Marcy C Speer; Jeffery Vance; F Lennon-Graham; Jeffrey M Stajich; Kristi D Viles; JM Gilchrist; V Nigro; R McMichael; J G Chutkow; L Bartoloni; stephen horrigan; Carol A Westbrook; Margaret Pericak-Vance
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
Human heredity 1998;48(4):179-84.
1998: Te-Cheng Pan; Rui-Zhu Zhang; Margaret Pericak-Vance; Rup Tandan; Timothy J Fries; Jeffrey M Stajich; Kristi D Viles; Jeffery Vance; Mon-Li Chu; Marcy C Speer
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 1998;7(5):807-12.
1996: Marcy C Speer; Rup Tandan; P N Rao; T Fries; Jeffrey M Stajich; PA Bolhuis; G Joost Jöbsis; Jeffery Vance; Kristi D Viles; K Sheffield; C James; SG Kahler; M Pettenati; John Gilbert; P H Denton; LH Yamaoka; Margaret Pericak-Vance
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.
Human molecular genetics 1996;5(7):1043-6.