Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 100

1.

A new rapid amplification of cDNA ends method for extremely guanine plus cytosine-rich genes.

Shi X, Jarvis DL.

Anal Biochem. 2006 Sep 15;356(2):222-8. Epub 2006 Jul 10.

2.

3' rapid amplification of cDNA ends (RACE) walking for rapid structural analysis of large transcripts.

Ozawa T, Kondo M, Isobe M.

J Hum Genet. 2004;49(2):102-5. Epub 2004 Jan 22.

PMID:
14740256
3.

Polymerase chain reaction optimization for amplification of Guanine-Cytosine rich templates using buccal cell DNA.

Bhagya CH, Wijesundera Sulochana WS, Hemamali NP.

Indian J Hum Genet. 2013 Jan;19(1):78-83. doi: 10.4103/0971-6866.112898.

4.

Polymerase reaction without primers throughout for the reconstruction of full-length cDNA from products of rapid amplification of cDNA ends (RACE).

Sunohara M, Kawakami M, Kage H, Watanabe K, Emoto N, Nagase T, Ohishi N, Takai D.

Biotechnol Lett. 2011 Jul;33(7):1301-7. doi: 10.1007/s10529-011-0580-1. Epub 2011 Mar 8.

PMID:
21384194
5.
6.

[Analysis of leader and trailer sequence of genotype III, VIb and VIId Newcastle disease virus determined by modified rapid amplification of cDNA ends (RACE) strategy].

Qiu X, Sun Q, Wang W, Dong L, Wu S, Hu S, Wu Y, Liu X.

Wei Sheng Wu Xue Bao. 2009 Jul;49(7):965-71. Chinese.

PMID:
19873764
7.

A new approach to touch down method using betaine as co-solvent for increased specificity and intensity of GC rich gene amplification.

Pratyush DD, Tiwari S, Kumar A, Singh SK.

Gene. 2012 Apr 15;497(2):269-72. doi: 10.1016/j.gene.2012.01.031. Epub 2012 Jan 28.

PMID:
22306261
8.
9.
10.

Rapid amplification of cDNA ends (RACE).

Yeku O, Frohman MA.

Methods Mol Biol. 2011;703:107-22. doi: 10.1007/978-1-59745-248-9_8.

PMID:
21125486
11.

Amplification of GC-rich genes by following a combination strategy of primer design, enhancers and modified PCR cycle conditions.

Sahdev S, Saini S, Tiwari P, Saxena S, Singh Saini K.

Mol Cell Probes. 2007 Aug;21(4):303-7. Epub 2007 Mar 30.

PMID:
17490855
12.

Reverse transcription slippage over the mRNA secondary structure of the LIP1 gene.

Zhang YJ, Pan HY, Gao SJ.

Biotechniques. 2001 Dec;31(6):1286, 1288, 1290, passim.

PMID:
11768657
13.

Multiple heat pulses during PCR extension enabling amplification of GC-rich sequences and reducing amplification bias.

Orpana AK, Ho TH, Stenman J.

Anal Chem. 2012 Feb 21;84(4):2081-7. doi: 10.1021/ac300040j. Epub 2012 Jan 30.

PMID:
22220596
14.

[Amplification of hepatitis C virus 5' untranslated region gene by RACE and its secondary structure analysis].

Qin Z, Cong X, Jiang D, Ha M, Chen H, Wei L.

Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2002 Dec;16(4):333-6. Chinese.

PMID:
12665898
15.

A guide for in-house design of template-switch-based 5' rapid amplification of cDNA ends systems.

Pinto FL, Lindblad P.

Anal Biochem. 2010 Feb 15;397(2):227-32. doi: 10.1016/j.ab.2009.10.022. Epub 2009 Nov 1.

PMID:
19837043
17.

famRCA-RACE: a rolling circle amplification race for isolating a family of homologous cDNAs in one reaction and its application to obtain NAC genes transcription factors from crocus (Crocus sativus) flower.

Kalivas A, Pasentsis K, Argiriou A, Darzentas N, Tsaftaris AS.

Prep Biochem Biotechnol. 2010;40(3):177-87. doi: 10.1080/10826068.2010.488507.

PMID:
20623429
18.

Amplification of mRNA populations by a cDNA tag strategy.

Sievertzon M, Agaton C, Nilsson P, Lundeberg J.

Biotechniques. 2004 Feb;36(2):253-9.

PMID:
14989090
19.

DMSO and betaine greatly improve amplification of GC-rich constructs in de novo synthesis.

Jensen MA, Fukushima M, Davis RW.

PLoS One. 2010 Jun 11;5(6):e11024. doi: 10.1371/journal.pone.0011024.

20.

The hepatitis C virus 5' untranslated region gene amplified by rapid amplification of cDNA ends and its secondary structure.

Qin ZX, Cong X, Jiang D, Ha MH, Chen HS, Wei L.

Hepatobiliary Pancreat Dis Int. 2002 Aug;1(3):368-72.

Items per page

Supplemental Content

Write to the Help Desk