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Items: 1 to 50 of 195

1.

Metakaryotic cells linked to pediatric pulmonary vein stenosis.

Kirkpatrick EC, Mitchell ME, Thilly WG, Hidestrand P, Tomita-Mitchell A, Hidestrand M, Gostjeva EV.

Cardiovasc Pathol. 2019 Mar - Apr;39:51-53. doi: 10.1016/j.carpath.2018.12.005. Epub 2018 Dec 21. No abstract available.

PMID:
30660022
2.

Restenosis in Hemodialytic Fistulas and Chronic Kidney Disease-Associated Vascular Disease: Two Pathologies Driven by Metakaryotic Stem Cells.

Pasquinelli G, Thilly WG, Gostjeva EV, Todeschini P, Cianciolo G, Ronco C, La Manna G.

Contrib Nephrol. 2017;190:96-107. doi: 10.1159/000468954. Epub 2017 May 23.

PMID:
28535522
3.

Mapping mitochondrial heteroplasmy in a Leydig tumor by laser capture micro-dissection and cycling temperature capillary electrophoresis.

Refinetti P, Arstad C, Thilly WG, Morgenthaler S, Ekstrøm PO.

BMC Clin Pathol. 2017 Apr 8;17:6. doi: 10.1186/s12907-017-0042-3. eCollection 2017.

4.

The study of calcified atherosclerotic arteries: an alternative to evaluate the composition of a problematic tissue reveals new insight including metakaryotic cells.

Fittipaldi S, Vasuri F, Degiovanni A, Pini R, Gargiulo M, Stella A, Pasquinelli G, Thilly WG, Gostjeva EV.

BMC Clin Pathol. 2016 Jul 29;16:12. doi: 10.1186/s12907-016-0036-6. eCollection 2016.

5.

Metakaryotic stem cell nuclei use pangenomic dsRNA/DNA intermediates in genome replication and segregation.

Thilly WG, Gostjeva EV, Koledova VV, Zukerberg LR, Chung D, Fomina JN, Darroudi F, Stollar BD.

Organogenesis. 2014 Jan 1;10(1):44-52. doi: 10.4161/org.27684. Epub 2014 Jan 13.

6.

Mutator/Hypermutable fetal/juvenile metakaryotic stem cells and human colorectal carcinogenesis.

Kini LG, Herrero-Jimenez P, Kamath T, Sanghvi J, Gutierrez E Jr, Hensle D, Kogel J, Kusko R, Rexer K, Kurzweil R, Refinetti P, Morgenthaler S, Koledova VV, Gostjeva EV, Thilly WG.

Front Oncol. 2013 Oct 29;3:267. doi: 10.3389/fonc.2013.00267. Review.

7.

Separation principles of cycling temperature capillary electrophoresis.

Ekstrøm PO, Warren DJ, Thilly WG.

Electrophoresis. 2012 Apr;33(7):1162-8. doi: 10.1002/elps.201100550.

PMID:
22539319
8.

Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids.

Gruhl AN, Gostjeva EV, Thilly WG, Fomina JN, Darroudi F.

Cancer Genet Cytogenet. 2010 Dec;203(2):203-8. doi: 10.1016/j.cancergencyto.2010.08.015.

9.

Non-invasive prenatal detection of trisomy 21 using tandem single nucleotide polymorphisms.

Ghanta S, Mitchell ME, Ames M, Hidestrand M, Simpson P, Goetsch M, Thilly WG, Struble CA, Tomita-Mitchell A.

PLoS One. 2010 Oct 8;5(10):e13184. doi: 10.1371/journal.pone.0013184.

10.

Metakaryotic stem cell lineages in organogenesis of humans and other metazoans.

Gostjeva EV, Koledova V, Tomita-Mitchell A, Mitchell M, Goetsch MA, Varmuza S, Fomina JN, Darroudi F, Thilly WG.

Organogenesis. 2009 Oct;5(4):191-200.

11.

Fetal-juvenile origins of point mutations in the adult human tracheal-bronchial epithelium: absence of detectable effects of age, gender or smoking status.

Sudo H, Li-Sucholeiki XC, Marcelino LA, Gruhl AN, Herrero-Jimenez P, Zarbl H, Willey JC, Furth EE, Morgenthaler S, Coller HA, Ekstrom PO, Kurzweil R, Gostjeva EV, Thilly WG.

Mutat Res. 2008 Nov 10;646(1-2):25-40. doi: 10.1016/j.mrfmmm.2008.08.016. Epub 2008 Sep 9.

PMID:
18824180
12.

Analysis of mutational spectra by denaturing capillary electrophoresis.

Ekstrøm PO, Khrapko K, Li-Sucholeiki XC, Hunter IW, Thilly WG.

Nat Protoc. 2008;3(7):1153-66. doi: 10.1038/nprot.2008.79.

14.

The human genomic melting map.

Liu F, Tøstesen E, Sundet JK, Jenssen TK, Bock C, Jerstad GI, Thilly WG, Hovig E.

PLoS Comput Biol. 2007 May;3(5):e93. Epub 2007 Apr 11.

15.

Correlations of asthma mortality with traffic-related factors: use of catalytic converters and radial tires.

Dorsey TF Jr, Lafleur AL, Kumata H, Takada H, Herrero-Jimenez P, Thilly WG.

J Occup Environ Med. 2006 Dec;48(12):1321-7.

PMID:
17159648
16.

Stem cell stages and the origins of colon cancer: a multidisciplinary perspective.

Gostjeva EV, Thilly WG.

Stem Cell Rev. 2005;1(3):243-51. Review.

PMID:
17142861
17.
18.

Origins of human mitochondrial point mutations as DNA polymerase gamma-mediated errors.

Zheng W, Khrapko K, Coller HA, Thilly WG, Copeland WC.

Mutat Res. 2006 Jul 25;599(1-2):11-20. Epub 2006 Feb 20.

PMID:
16490220
19.

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.

Mutat Res. 2006 Apr 11;596(1-2):113-27. Epub 2006 Feb 3.

PMID:
16458330
20.
21.

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.

J Sep Sci. 2005 Aug;28(12):1375-89.

PMID:
16138690
22.

Real-time PCR measurement by fluorescence anisotropy.

Crane BL, Hogan NC, Sudo H, Thilly WG, Hunter IW.

Anal Chem. 2005 Aug 15;77(16):5129-34.

PMID:
16097749
23.

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.

Mutat Res. 2005 Oct 15;578(1-2):256-71. Epub 2005 Jul 11.

PMID:
16009384
24.

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.

Electrophoresis. 2005 Jun;26(13):2531-8.

PMID:
15948210
25.

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.

Mutat Res. 2005 Mar 1;570(2):267-80.

PMID:
15708585
26.

Multistage carcinogenesis and the fraction at risk.

Morgenthaler S, Herrero P, Thilly WG.

J Math Biol. 2004 Nov;49(5):455-67. Epub 2004 Apr 23.

PMID:
15549309
27.
28.

The mutational spectrum of the HPRT gene from human T cells in vivo shares a significant concordant set of hot spots with MNNG-treated human cells.

Tomita-Mitchell A, Ling LL, Glover CL, Goodluck-Griffith J, Thilly WG.

Cancer Res. 2003 Sep 15;63(18):5793-8.

30.

Have environmental mutagens caused oncomutations in people?

Thilly WG.

Nat Genet. 2003 Jul;34(3):255-9. Review.

PMID:
12833049
31.

Quantitative detection of benzo[alpha]pyrene diolepoxide-DNA adducts by cryogenic laser induced fluorescence.

Luo W, Gurjuar R, Ozbal C, Taghizadeh K, Lafleur A, Dasari RR, Zarbl H, Thilly WG.

Chem Res Toxicol. 2003 Jan;16(1):74-80.

PMID:
12693033
32.

High-efficiency DNA ligation for clamp attachment without polymerase chain reaction.

Kim AS, Holmquist GP, Thilly WG.

Anal Biochem. 2002 Nov 15;310(2):179-85.

PMID:
12423636
34.

Scanning low-frequency point mutants in the mitochondrial genome using constant denaturant capillary electrophoresis.

Zheng W, Marcelino LA, Thilly WG.

Methods Mol Biol. 2002;197:93-106. No abstract available.

PMID:
12013815
35.
37.

High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection.

Coller HA, Khrapko K, Bodyak ND, Nekhaeva E, Herrero-Jimenez P, Thilly WG.

Nat Genet. 2001 Jun;28(2):147-50.

PMID:
11381261
38.

High resolution analysis of point mutations by constant denaturant capillary electrophoresis (CDCE).

Khrapko K, Coller HA, Li-Sucholeiki XC, André PC, Thilly WG.

Methods Mol Biol. 2001;163:57-72. No abstract available.

PMID:
11242964
39.

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

Kim AS, Li-Sucholeiki XC, Thilly WG.

Methods Mol Biol. 2001;163:175-89. No abstract available.

PMID:
11242942
40.

Two-point fluorescence detection and automated fraction collection applied to constant denaturant capillary electrophoresis.

Ekstrøm PO, Wasserkort R, Minarik M, Foret F, Thilly WG.

Biotechniques. 2000 Sep;29(3):582-4, 586-9.

41.

Identification of in vivo mutations in exon 5 of the human HPRT gene in a set of pooled T-cell mutants by constant denaturant capillary electrophoresis (CDCE).

Fält S, Kumar R, Wennborg A, Tomita-Mitchell A, Thilly WG, Lambert B.

Mutat Res. 2000 Jul 20;452(1):57-66.

PMID:
10894891
42.

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.

Mutat Res. 2000 May 30;450(1-2):125-38.

PMID:
10838138
43.
44.

Normal bronchial epithelial cell expression of glutathione transferase P1, glutathione transferase M3, and glutathione peroxidase is low in subjects with bronchogenic carcinoma.

Crawford EL, Khuder SA, Durham SJ, Frampton M, Utell M, Thilly WG, Weaver DA, Ferencak WJ, Jennings CA, Hammersley JR, Olson DA, Willey JC.

Cancer Res. 2000 Mar 15;60(6):1609-18.

45.

Population risk and physiological rate parameters for colon cancer. The union of an explicit model for carcinogenesis with the public health records of the United States.

Herrero-Jimenez P, Tomita-Mitchell A, Furth EE, Morgenthaler S, Thilly WG.

Mutat Res. 2000 Jan 17;447(1):73-116.

PMID:
10686307
46.

Mitochondrial mutagenesis in human cells and tissues.

Marcelino LA, Thilly WG.

Mutat Res. 1999 Jul 30;434(3):177-203. Review. No abstract available.

PMID:
10486591
47.

Detection of low-frequency mutations in exon 8 of the TP53 gene by constant denaturant capillary electrophoresis (CDCE).

Ekstrøm PO, Børresen-Dale AL, Qvist H, Giercksky KE, Thilly WG.

Biotechniques. 1999 Jul;27(1):128-34.

48.

Applications of constant denaturant capillary electrophoresis/high-fidelity polymerase chain reaction to human genetic analysis.

Li-Sucholeiki XC, Khrapko K, André PC, Marcelino LA, Karger BL, Thilly WG.

Electrophoresis. 1999 Jun;20(6):1224-32. Review.

PMID:
10380762
49.

Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions.

Khrapko K, Bodyak N, Thilly WG, van Orsouw NJ, Zhang X, Coller HA, Perls TT, Upton M, Vijg J, Wei JY.

Nucleic Acids Res. 1999 Jun 1;27(11):2434-41.

50.

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