Format
Items per page
Sort by

Send to:

Choose Destination

Selected items

Items: 20

1.

Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18.

Ashoor G, Syngelaki A, Wagner M, Birdir C, Nicolaides KH.

Am J Obstet Gynecol. 2012 Apr;206(4):322.e1-5. doi: 10.1016/j.ajog.2012.01.029. Epub 2012 Jan 24.

PMID:
22464073
2.

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.

Bianchi DW, Platt LD, Goldberg JD, Abuhamad AZ, Sehnert AJ, Rava RP; MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group.

Obstet Gynecol. 2012 May;119(5):890-901. doi: 10.1097/AOG.0b013e31824fb482. Erratum in: Obstet Gynecol. 2012 Oct;120(4):957.

PMID:
22362253
3.

DNA-protein interactions: methods for detection and analysis.

Dey B, Thukral S, Krishnan S, Chakrobarty M, Gupta S, Manghani C, Rani V.

Mol Cell Biochem. 2012 Jun;365(1-2):279-99. doi: 10.1007/s11010-012-1269-z. Epub 2012 Mar 8. Review.

PMID:
22399265
4.

Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

Sparks AB, Struble CA, Wang ET, Song K, Oliphant A.

Am J Obstet Gynecol. 2012 Apr;206(4):319.e1-9. doi: 10.1016/j.ajog.2012.01.030. Epub 2012 Jan 26.

PMID:
22464072
5.

Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Southern EM.

J Mol Biol. 1975 Nov 5;98(3):503-17. No abstract available.

PMID:
1195397
6.

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting.

Ehrich M, Deciu C, Zwiefelhofer T, Tynan JA, Cagasan L, Tim R, Lu V, McCullough R, McCarthy E, Nygren AO, Dean J, Tang L, Hutchison D, Lu T, Wang H, Angkachatchai V, Oeth P, Cantor CR, Bombard A, van den Boom D.

Am J Obstet Gynecol. 2011 Mar;204(3):205.e1-11. doi: 10.1016/j.ajog.2010.12.060. Epub 2011 Feb 18.

PMID:
21310373
7.

A new rapid method for Clostridium difficile DNA extraction and detection in stool: toward point-of-care diagnostic testing.

Freifeld AG, Simonsen KA, Booth CS, Zhao X, Whitney SE, Karre T, Iwen PC, Viljoen HJ.

J Mol Diagn. 2012 May-Jun;14(3):274-9. doi: 10.1016/j.jmoldx.2012.01.003. Epub 2012 Mar 5.

8.
9.

Direct detection of DNA methylation during single-molecule, real-time sequencing.

Flusberg BA, Webster DR, Lee JH, Travers KJ, Olivares EC, Clark TA, Korlach J, Turner SW.

Nat Methods. 2010 Jun;7(6):461-5. doi: 10.1038/nmeth.1459. Epub 2010 May 9.

11.

Detection rates of precancerous and cancerous cervical lesions within one screening round of primary human papillomavirus DNA testing: prospective randomised trial in Finland.

Leinonen MK, Nieminen P, Lönnberg S, Malila N, Hakama M, Pokhrel A, Laurila P, Tarkkanen J, Anttila A.

BMJ. 2012 Nov 29;345:e7789. doi: 10.1136/bmj.e7789.

12.

Sensitive and specific detection of Trypanosoma cruzi DNA in clinical specimens using a multi-target real-time PCR approach.

Qvarnstrom Y, Schijman AG, Veron V, Aznar C, Steurer F, da Silva AJ.

PLoS Negl Trop Dis. 2012;6(7):e1689. doi: 10.1371/journal.pntd.0001689. Epub 2012 Jul 3.

14.

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T.

Proc Natl Acad Sci U S A. 1989 Apr;86(8):2766-70.

15.

Detection of promoter methylation of tumor suppressor genes in serum DNA of breast cancer cases and benign breast disease controls.

Sturgeon SR, Balasubramanian R, Schairer C, Muss HB, Ziegler RG, Arcaro KF.

Epigenetics. 2012 Nov;7(11):1258-67. doi: 10.4161/epi.22220. Epub 2012 Sep 17.

16.

Protein detection using proximity-dependent DNA ligation assays.

Fredriksson S, Gullberg M, Jarvius J, Olsson C, Pietras K, Gústafsdóttir SM, Ostman A, Landegren U.

Nat Biotechnol. 2002 May;20(5):473-7.

PMID:
11981560
17.

Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood.

Sehnert AJ, Rhees B, Comstock D, de Feo E, Heilek G, Burke J, Rava RP.

Clin Chem. 2011 Jul;57(7):1042-9. doi: 10.1373/clinchem.2011.165910. Epub 2011 Apr 25.

18.

A chemical method for fast and sensitive detection of DNA synthesis in vivo.

Salic A, Mitchison TJ.

Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2415-20. doi: 10.1073/pnas.0712168105. Epub 2008 Feb 12.

19.

Fluorescence detection in automated DNA sequence analysis.

Smith LM, Sanders JZ, Kaiser RJ, Hughes P, Dodd C, Connell CR, Heiner C, Kent SB, Hood LE.

Nature. 1986 Jun 12-18;321(6071):674-9.

PMID:
3713851
20.

International study to evaluate PCR methods for detection of Trypanosoma cruzi DNA in blood samples from Chagas disease patients.

Schijman AG, Bisio M, Orellana L, Sued M, Duffy T, Mejia Jaramillo AM, Cura C, Auter F, Veron V, Qvarnstrom Y, Deborggraeve S, Hijar G, Zulantay I, Lucero RH, Velazquez E, Tellez T, Sanchez Leon Z, Galvão L, Nolder D, Monje Rumi M, Levi JE, Ramirez JD, Zorrilla P, Flores M, Jercic MI, Crisante G, Añez N, De Castro AM, Gonzalez CI, Acosta Viana K, Yachelini P, Torrico F, Robello C, Diosque P, Triana Chavez O, Aznar C, Russomando G, Büscher P, Assal A, Guhl F, Sosa Estani S, DaSilva A, Britto C, Luquetti A, Ladzins J.

PLoS Negl Trop Dis. 2011 Jan 11;5(1):e931. doi: 10.1371/journal.pntd.0000931.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk