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Methylation analysis by microarray.

Methods in molecular biology (Clifton, N.J.)

Deatherage DE, Potter D, Yan PS, Huang TH, Lin S.
PMID: 19488875
Methods Mol Biol. 2009;556:117-39. doi: 10.1007/978-1-60327-192-9_9.

Differential methylation hybridization (DMH) is a high-throughput DNA methylation screening tool that utilizes methylation-sensitive restriction enzymes to profile methylated fragments by hybridizing them to a CpG island microarray. This array contains probes spanning all the 27,800 islands annotated in...

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Deatherage DE, Potter D, Yan PS, et al. Methylation analysis by microarray. Methods Mol Biol. 2009;556:117-39doi: 10.1007/978-1-60327-192-9_9.
Deatherage, D. E., Potter, D., Yan, P. S., Huang, T. H., & Lin, S. (2009). Methylation analysis by microarray. Methods in molecular biology (Clifton, N.J.), 556117-39. https://doi.org/10.1007/978-1-60327-192-9_9
Deatherage, Daniel E, et al. "Methylation analysis by microarray." Methods in molecular biology (Clifton, N.J.) vol. 556 (2009): 117-39. doi: https://doi.org/10.1007/978-1-60327-192-9_9
Deatherage DE, Potter D, Yan PS, Huang TH, Lin S. Methylation analysis by microarray. Methods Mol Biol. 2009;556:117-39. doi: 10.1007/978-1-60327-192-9_9. PMID: 19488875; PMCID: PMC2838393.
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Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies.

Analytical and bioanalytical chemistry

Dufva M, Petersen J, Poulsen L.
PMID: 19495730
Anal Bioanal Chem. 2009 Oct;395(3):669-77. doi: 10.1007/s00216-009-2848-z. Epub 2009 Jun 03.

DNA microarrays have for a decade been the only platform for genome-wide analysis and have provided a wealth of information about living organisms. DNA microarrays are processed today under one condition only, which puts large demands on assay development...

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Dufva M, Petersen J, Poulsen L. Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies. Anal Bioanal Chem. 2009;395(3):669-77doi: 10.1007/s00216-009-2848-z.
Dufva, M., Petersen, J., & Poulsen, L. (2009). Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies. Analytical and bioanalytical chemistry, 395(3), 669-77. https://doi.org/10.1007/s00216-009-2848-z
Dufva, Martin, et al. "Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies." Analytical and bioanalytical chemistry vol. 395,3 (2009): 669-77. doi: https://doi.org/10.1007/s00216-009-2848-z
Dufva M, Petersen J, Poulsen L. Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies. Anal Bioanal Chem. 2009 Oct;395(3):669-77. doi: 10.1007/s00216-009-2848-z. Epub 2009 Jun 03. PMID: 19495730.
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DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samples.

Analytical chemistry

Le Roux D, Root BE, Reedy CR, Hickey JA, Scott ON, Bienvenue JM, Landers JP, Chassagne L, de Mazancourt P.
PMID: 25091472
Anal Chem. 2014 Aug 19;86(16):8192-9. doi: 10.1021/ac501666b. Epub 2014 Aug 05.

A system that automatically performs the PCR amplification and microchip electrophoretic (ME) separation for rapid forensic short tandem repeat (STR) forensic profiling in a single disposable plastic chip is demonstrated. The microchip subassays were optimized to deliver results comparable...

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Le Roux D, Root BE, Reedy CR, et al. DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samples. Anal Chem. 2014;86(16):8192-9doi: 10.1021/ac501666b.
Le Roux, D., Root, B. E., Reedy, C. R., Hickey, J. A., Scott, O. N., Bienvenue, J. M., Landers, J. P., Chassagne, L., & de Mazancourt, P. (2014). DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samples. Analytical chemistry, 86(16), 8192-9. https://doi.org/10.1021/ac501666b
Le Roux, Delphine, et al. "DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samples." Analytical chemistry vol. 86,16 (2014): 8192-9. doi: https://doi.org/10.1021/ac501666b
Le Roux D, Root BE, Reedy CR, Hickey JA, Scott ON, Bienvenue JM, Landers JP, Chassagne L, de Mazancourt P. DNA analysis using an integrated microchip for multiplex PCR amplification and electrophoresis for reference samples. Anal Chem. 2014 Aug 19;86(16):8192-9. doi: 10.1021/ac501666b. Epub 2014 Aug 05. PMID: 25091472.
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Circular dichroism spectroscopy of DNA duplexes at near-biological concentrations.

Bioorganic & medicinal chemistry letters

Vanloon J, Harroun T, Yan H.
PMID: 33895278
Bioorg Med Chem Lett. 2021 Jul 01;43:128053. doi: 10.1016/j.bmcl.2021.128053. Epub 2021 Apr 22.

Circular dichroism (CD) of nucleic acids has been typically carried out at sample concentrations below 10 μM, which is far lower than nucleic acid concentrations in biological systems. Attempts to study nucleic acid conformations by CD at higher concentrations...

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Vanloon J, Harroun T, Yan H. Circular dichroism spectroscopy of DNA duplexes at near-biological concentrations. Bioorg Med Chem Lett. 2021;43:128053doi: 10.1016/j.bmcl.2021.128053.
Vanloon, J., Harroun, T., & Yan, H. (2021). Circular dichroism spectroscopy of DNA duplexes at near-biological concentrations. Bioorganic & medicinal chemistry letters, 43128053. https://doi.org/10.1016/j.bmcl.2021.128053
Vanloon, Jesse, et al. "Circular dichroism spectroscopy of DNA duplexes at near-biological concentrations." Bioorganic & medicinal chemistry letters vol. 43 (2021): 128053. doi: https://doi.org/10.1016/j.bmcl.2021.128053
Vanloon J, Harroun T, Yan H. Circular dichroism spectroscopy of DNA duplexes at near-biological concentrations. Bioorg Med Chem Lett. 2021 Jul 01;43:128053. doi: 10.1016/j.bmcl.2021.128053. Epub 2021 Apr 22. PMID: 33895278.
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Additive manufacturing of laminar flow cells for single-molecule experiments.

Scientific reports

Ahmadi A, Till K, Hafting Y, Schüttpelz M, Bjørås M, Glette K, Tørresen J, Rowe AD, Dalhus B.
PMID: 31727950
Sci Rep. 2019 Nov 14;9(1):16784. doi: 10.1038/s41598-019-53151-z.

A microfluidic laminar flow cell (LFC) forms an indispensable component in single-molecule experiments, enabling different substances to be delivered directly to the point under observation and thereby tightly controlling the biochemical environment immediately surrounding single molecules. Despite substantial progress...

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Ahmadi A, Till K, Hafting Y, et al. Additive manufacturing of laminar flow cells for single-molecule experiments. Sci Rep. 2019;9(1):16784doi: 10.1038/s41598-019-53151-z.
Ahmadi, A., Till, K., Hafting, Y., Schüttpelz, M., Bjørås, M., Glette, K., Tørresen, J., Rowe, A. D., & Dalhus, B. (2019). Additive manufacturing of laminar flow cells for single-molecule experiments. Scientific reports, 9(1), 16784. https://doi.org/10.1038/s41598-019-53151-z
Ahmadi, Arash, et al. "Additive manufacturing of laminar flow cells for single-molecule experiments." Scientific reports vol. 9,1 (2019): 16784. doi: https://doi.org/10.1038/s41598-019-53151-z
Ahmadi A, Till K, Hafting Y, Schüttpelz M, Bjørås M, Glette K, Tørresen J, Rowe AD, Dalhus B. Additive manufacturing of laminar flow cells for single-molecule experiments. Sci Rep. 2019 Nov 14;9(1):16784. doi: 10.1038/s41598-019-53151-z. PMID: 31727950; PMCID: PMC6856346.
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DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps.

JAMA

Murray MF, Evans JP, Khoury MJ.
PMID: 31808788
JAMA. 2020 Jan 28;323(4):307-308. doi: 10.1001/jama.2019.18640.

No abstract available.

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Murray MF, Evans JP, Khoury MJ. DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps. JAMA. 2020;323(4):307-308doi: 10.1001/jama.2019.18640.
Murray, M. F., Evans, J. P., & Khoury, M. J. (2020). DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps. JAMA, 323(4), 307-308. https://doi.org/10.1001/jama.2019.18640
Murray, Michael F, et al. "DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps." JAMA vol. 323,4 (2020): 307-308. doi: https://doi.org/10.1001/jama.2019.18640
Murray MF, Evans JP, Khoury MJ. DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps. JAMA. 2020 Jan 28;323(4):307-308. doi: 10.1001/jama.2019.18640. PMID: 31808788.
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Label-free plasmonic assisted optical trapping of single DNA molecules.

Optics letters

Chen L, Liu W, Shen D, Zhou Z, Liu Y, Wan W.
PMID: 33720217
Opt Lett. 2021 Mar 15;46(6):1482-1485. doi: 10.1364/OL.420957.

DNA molecules are hard to catch using traditional optical trapping due to the nanometer width of their chains. Here we experimentally demonstrate a label-free optical trapping of a single micrometer

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Chen L, Liu W, Shen D, et al. Label-free plasmonic assisted optical trapping of single DNA molecules. Opt Lett. 2021;46(6):1482-1485doi: 10.1364/OL.420957.
Chen, L., Liu, W., Shen, D., Zhou, Z., Liu, Y., & Wan, W. (2021). Label-free plasmonic assisted optical trapping of single DNA molecules. Optics letters, 46(6), 1482-1485. https://doi.org/10.1364/OL.420957
Chen, Lei, et al. "Label-free plasmonic assisted optical trapping of single DNA molecules." Optics letters vol. 46,6 (2021): 1482-1485. doi: https://doi.org/10.1364/OL.420957
Chen L, Liu W, Shen D, Zhou Z, Liu Y, Wan W. Label-free plasmonic assisted optical trapping of single DNA molecules. Opt Lett. 2021 Mar 15;46(6):1482-1485. doi: 10.1364/OL.420957. PMID: 33720217.
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Microarrays: their origins and applications.

Trends in biotechnology

Ekins R, Chu FW.
PMID: 10354556
Trends Biotechnol. 1999 Jun;17(6):217-8. doi: 10.1016/s0167-7799(99)01329-3.

No abstract available.

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Ekins R, Chu FW. Microarrays: their origins and applications. Trends Biotechnol. 1999;17(6):217-8doi: 10.1016/s0167-7799(99)01329-3.
Ekins, R., & Chu, F. W. (1999). Microarrays: their origins and applications. Trends in biotechnology, 17(6), 217-8. https://doi.org/10.1016/s0167-7799(99)01329-3
Ekins, R, and Chu, F W. "Microarrays: their origins and applications." Trends in biotechnology vol. 17,6 (1999): 217-8. doi: https://doi.org/10.1016/s0167-7799(99)01329-3
Ekins R, Chu FW. Microarrays: their origins and applications. Trends Biotechnol. 1999 Jun;17(6):217-8. doi: 10.1016/s0167-7799(99)01329-3. PMID: 10354556.
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[DNA diagnosis for eye diseases at the present time and in the future].

Nippon Ganka Gakkai zasshi

Mashima Y.
PMID: 11579583
Nippon Ganka Gakkai Zasshi. 2001 Sep;105(9):589-90.

No abstract available.

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Mashima Y. [DNA diagnosis for eye diseases at the present time and in the future]. Nippon Ganka Gakkai Zasshi. 2001;105(9):589-90
Mashima, Y. (2001). [DNA diagnosis for eye diseases at the present time and in the future]. Nippon Ganka Gakkai zasshi, 105(9), 589-90.
Mashima, Y. "[DNA diagnosis for eye diseases at the present time and in the future]." Nippon Ganka Gakkai zasshi vol. 105,9 (2001): 589-90.
Mashima Y. [DNA diagnosis for eye diseases at the present time and in the future]. Nippon Ganka Gakkai Zasshi. 2001 Sep;105(9):589-90. Japanese. PMID: 11579583.
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Computer chip speeds DNA analysis.

Analytical chemistry

[No authors listed]
PMID: 2757216
Anal Chem. 1989 Jul 15;61(14):834A. doi: 10.1021/ac00189a719.

No abstract available.

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Computer chip speeds DNA analysis. Anal Chem. 1989;61(14):834Adoi: 10.1021/ac00189a719.
(1989). Computer chip speeds DNA analysis. Analytical chemistry, 61(14), 834A. https://doi.org/10.1021/ac00189a719
"Computer chip speeds DNA analysis." Analytical chemistry vol. 61,14 (1989): 834A. doi: https://doi.org/10.1021/ac00189a719
Computer chip speeds DNA analysis. Anal Chem. 1989 Jul 15;61(14):834A. doi: 10.1021/ac00189a719. PMID: 2757216.
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DNA typing is called flawed.

Science (New York, N.Y.)

Lewin R.
PMID: 2756424
Science. 1989 Jul 28;245(4916):355. doi: 10.1126/science.2756424.

No abstract available.

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Lewin R. DNA typing is called flawed. Science. 1989;245(4916):355doi: 10.1126/science.2756424.
Lewin, R. (1989). DNA typing is called flawed. Science (New York, N.Y.), 245(4916), 355. https://doi.org/10.1126/science.2756424
Lewin, R. "DNA typing is called flawed." Science (New York, N.Y.) vol. 245,4916 (1989): 355. doi: https://doi.org/10.1126/science.2756424
Lewin R. DNA typing is called flawed. Science. 1989 Jul 28;245(4916):355. doi: 10.1126/science.2756424. PMID: 2756424.
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On the shape of a DNA molecule.

The Bulletin of mathematical biophysics

Wu TT.
PMID: 5963155
Bull Math Biophys. 1966 Jun;28(2):207-16. doi: 10.1007/BF02476995.

No abstract available.

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Wu TT. On the shape of a DNA molecule. Bull Math Biophys. 1966;28(2):207-16doi: 10.1007/BF02476995.
Wu, T. T. (1966). On the shape of a DNA molecule. The Bulletin of mathematical biophysics, 28(2), 207-16. https://doi.org/10.1007/BF02476995
Wu, T T. "On the shape of a DNA molecule." The Bulletin of mathematical biophysics vol. 28,2 (1966): 207-16. doi: https://doi.org/10.1007/BF02476995
Wu TT. On the shape of a DNA molecule. Bull Math Biophys. 1966 Jun;28(2):207-16. doi: 10.1007/BF02476995. PMID: 5963155.
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Showing 1 to 12 of 67 entries