Thilly WG - Search Results

1

Detection and frequency estimation of rare variants in pools of genomic DNA from large populations using mutational spectrometry.

Li-Sucholeiki XC, Tomita-Mitchell A, Arnold K, Glassner BJ, Thompson T, Murthy JV, Berk L, Lange C, Leong-Morgenthaler PM, MacDougall D, Munro J, Cannon D, Mistry T, Miller A, Deka C, Karger B, Gillespie KM, Ekstrøm PO, Todd JA, Thilly WG. Li-Sucholeiki XC, et al. Among authors: thilly wg. Mutat Res. 2005 Mar 1;570(2):267-80. doi: 10.1016/j.mrfmmm.2004.11.004. Mutat Res. 2005. PMID: 15708585

2

A sensitive scanning technology for low frequency nuclear point mutations in human genomic DNA.

Li-Sucholeiki XC, Thilly WG. Li-Sucholeiki XC, et al. Among authors: thilly wg. Nucleic Acids Res. 2000 May 1;28(9):E44. doi: 10.1093/nar/28.9.e44. Nucleic Acids Res. 2000. PMID: 10756211 Free PMC article.

3

Mismatch repair deficient human cells: spontaneous and MNNG-induced mutational spectra in the HPRT gene.

Tomita-Mitchell A, Kat AG, Marcelino LA, Li-Sucholeiki XC, Goodluck-Griffith J, Thilly WG. Tomita-Mitchell A, et al. Among authors: thilly wg. Mutat Res. 2000 May 30;450(1-2):125-38. doi: 10.1016/s0027-5107(00)00020-8. Mutat Res. 2000. PMID: 10838138

4

Scanning the beta-globin gene for mutations in large populations by denaturing capillary and gel electrophoresis.

Li-Sucholeiki XC, Hu G, Perls T, Tomita-Mitchell A, Thilly WG. Li-Sucholeiki XC, et al. Among authors: thilly wg. Electrophoresis. 2005 Jun;26(13):2531-8. doi: 10.1002/elps.200410431. Electrophoresis. 2005. PMID: 15948210

5

Clustering of mutant mitochondrial DNA copies suggests stem cells are common in human bronchial epithelium.

Coller HA, Khrapko K, Herrero-Jimenez P, Vatland JA, Li-Sucholeiki XC, Thilly WG. Coller HA, et al. Among authors: thilly wg. Mutat Res. 2005 Oct 15;578(1-2):256-71. doi: 10.1016/j.mrfmmm.2005.05.014. Epub 2005 Jul 11. Mutat Res. 2005. PMID: 16009384

6

Distributions of five common point mutants in the human tracheal-bronchial epithelium.

Sudo H, Li-Sucholeiki XC, Marcelino LA, Gruhl AN, Zarbl H, Willey JC, Thilly WG. Sudo H, et al. Among authors: thilly wg. Mutat Res. 2006 Apr 11;596(1-2):113-27. doi: 10.1016/j.mrfmmm.2005.12.008. Epub 2006 Feb 3. Mutat Res. 2006. PMID: 16458330

7

Analysis of mutational spectra by denaturing capillary electrophoresis.

Ekstrøm PO, Khrapko K, Li-Sucholeiki XC, Hunter IW, Thilly WG. Ekstrøm PO, et al. Among authors: thilly wg. Nat Protoc. 2008;3(7):1153-66. doi: 10.1038/nprot.2008.79. Nat Protoc. 2008. PMID: 18600220 Free PMC article.

8

Applications of constant denaturant capillary electrophoresis and complementary procedures. Measurement of point mutational spectra.

Kim AS, Li-Sucholeiki XC, Thilly WG. Kim AS, et al. Among authors: thilly wg. Methods Mol Biol. 2001;163:175-89. doi: 10.1385/1-59259-116-7:175. Methods Mol Biol. 2001. PMID: 11242942 No abstract available.

9

Design of an automated multicapillary instrument with fraction collection for DNA mutation discovery by constant denaturant capillary electrophoresis (CDCE).

Li Q, Deka C, Glassner BJ, Arnold K, Li-Sucholeiki XC, Tomita-Mitchell A, Thilly WG, Karger BL. Li Q, et al. Among authors: thilly wg. J Sep Sci. 2005 Aug;28(12):1375-89. doi: 10.1002/jssc.200500023. J Sep Sci. 2005. PMID: 16138690

10

Technology to accelerate pangenomic scanning for unknown point mutations in exonic sequences: cycling temperature capillary electrophoresis (CTCE).

Ekstrøm PO, Bjørheim J, Thilly WG. Ekstrøm PO, et al. Among authors: thilly wg. BMC Genet. 2007 Aug 14;8:54. doi: 10.1186/1471-2156-8-54. BMC Genet. 2007. PMID: 17697348 Free PMC article.

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