The use of polymerase chain reaction generated nucleotide sequences as probes for hybridization
- 31 December 1990
- journal article
- Published by Elsevier in Molecular and Cellular Probes
- Vol. 4 (6) , 485-495
- https://doi.org/10.1016/0890-8508(90)90007-m
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Use of an RNA folding algorithm to choose regions for amplification by the polymerase chain reactionAnalytical Biochemistry, 1990
- Isolation and analysis of ribonucleic acids from skeletal tissuesAnalytical Biochemistry, 1989
- Estrogen receptor mRNA expression in callus during fracture healing in the ratCalcified Tissue International, 1989
- Wound Macrophages Express TGF-α and Other Growth Factors in Vivo: Analysis by mRNA PhenotypingScience, 1988
- Localization of types I, II, and III collagen mRNAs in developing human skeletal tissues by in situ hybridizationThe Journal of cell biology, 1987
- Efficiency of in situ hybridization as a function of probe size and fixation techniqueJournal of Virological Methods, 1985
- Efficientin vitrosynthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoterNucleic Acids Research, 1984
- Optimal computer folding of large RNA sequences using thermodynamics and auxiliary informationNucleic Acids Research, 1981
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesisTetrahedron Letters, 1981