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Items: 1 to 20 of 169

1.

Overcoming limitations of the mRNA differential display technique.

Sompayrac L, Jane S, Burn TC, Tenen DG, Danna KJ.

Nucleic Acids Res. 1995 Nov 25;23(22):4738-9. No abstract available.

2.

Modifications to the differential display technique reduce background and increase sensitivity.

Hadman M, Adam BL, Wright GL Jr, Bos TJ.

Anal Biochem. 1995 Apr 10;226(2):383-6. No abstract available.

PMID:
7540811
3.

Analysis of altered gene expression by differential display.

Liang P, Bauer D, Averboukh L, Warthoe P, Rohrwild M, Muller H, Strauss M, Pardee AB.

Methods Enzymol. 1995;254:304-21. No abstract available.

PMID:
8531695
4.

Use of 33P-labeled primer increases the sensitivity and specificity of mRNA differential display.

Tokuyama Y, Takeda J.

Biotechniques. 1995 Mar;18(3):424-5. No abstract available.

PMID:
7540020
5.

Analysis of promoter activity by polymerase chain reaction amplification of reporter gene mRNA.

Kastenbauer S, Wedel A, Frankenberger M, Wirth T, Ziegler-Heitbrock HW.

Anal Biochem. 1996 Jan 1;233(1):137-9. No abstract available.

PMID:
8789158
6.

Detection of a proliferation specific gene during development of the osteoblast phenotype by mRNA differential display.

Ryoo HM, van Wijnen AJ, Stein JL, Lian JB, Stein GS.

J Cell Biochem. 1997 Jan;64(1):106-16.

PMID:
9015759
7.

Differential display PCR: a new age in nutrition investigation.

Harris ED.

Nutr Rev. 1996 Sep;54(9):287-9. Review.

PMID:
9009671
8.

New primer strategy improves precision of differential display.

Zhao S, Ooi SL, Pardee AB.

Biotechniques. 1995 May;18(5):842-6, 848, 850.

PMID:
7619490
9.

Simple and rapid 5' and 3' extension techniques in RT-PCR.

Struck F, Collins J.

Nucleic Acids Res. 1994 May 25;22(10):1923-4. No abstract available.

10.

The use of reverse transcription polymerase chain reaction to analyse large numbers of mRNA species from a single cell.

Toellner KM, Scheel-Toellner D, Seitzer U, Sprenger R, Trümper L, Schlüter C, Flad HD, Gerdes J.

J Immunol Methods. 1996 May 10;191(1):71-5.

PMID:
8642203
12.

Isolation of genetic suppressor elements (GSEs) from random fragment cDNA libraries in retroviral vectors.

Gudkov AV, Roninson IB.

Methods Mol Biol. 1997;69:221-40. No abstract available.

PMID:
9116855
13.

The expression of truncated MK in human tumors.

Kaname T, Kadomatsu K, Aridome K, Yamashita S, Sakamoto K, Ogawa M, Muramatsu T, Yamamura K.

Biochem Biophys Res Commun. 1996 Feb 6;219(1):256-60.

PMID:
8619817
14.

A method for rapid generation of competitive standard molecules for RT-PCR avoiding the problem of competitor/probe cross-reactions.

Ross R, Kleiz R, Reske-Kunz AB.

PCR Methods Appl. 1995 Jun;4(6):371-5. No abstract available.

16.
17.

In vivo footprinting of the interaction of proteins with DNA and RNA.

Grange T, Bertrand E, Espinás ML, Fromont-Racine M, Rigaud G, Roux J, Pictet R.

Methods. 1997 Feb;11(2):151-63.

PMID:
8993027
18.
19.

Triple primer polymerase chain reaction. A new way to quantify truncated mRNA expression.

Leygue E, Murphy L, Kuttenn F, Watson P.

Am J Pathol. 1996 Apr;148(4):1097-103.

20.

Identification of genes regulated by glucose in a pancreatic beta-cell line by a new method for subtraction of mRNA.

Yamato E, Ikegami H, Miyazaki JI, Ogihara T.

Diabetologia. 1996 Nov;39(11):1293-8.

PMID:
8932994

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