1. Alu polymerase chain reaction is enormously valuable.

2. Details of the polymerase chain reaction are given in a previous publication.

3. A thermostable DNA polymerase is added to the same tube.

4. T3 symbolizes the T3 RNA polymerase promoter of a bluescript plasmid.

5. Polymerase chain reaction, however, is a powerful technique capable of amplifying specific target DNA sequences by a factor of 10.

6. Inhibits platelet aggregation. DNA polymerase inhibitor. Shows antifungal activity.

7. Component of prokaryotic RNA polymerase holoenzyme.

8. "bubble" formed by RNA polymerase move in 10s?

9. Telomerase is RNA dependent DNA polymerase, acts to synthesize DNA repeat fragment of telomeres , which is associated with immortalization of cells.

10. Genome DNA was extracted from white blood cell. Polymerase chain reaction (PCR) and restriction fragment-length polymorphism (RFLP) were employed to study C-344T polymorphism of CYP11B2 gene.

11. Objective Polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) assay was applied to molecular typing of resistance-associated esterase genes of Culex pipiens complex.

12. Objective: To establish polymerase chain reaction -gel documentation system (PCR-GDS) technology for detecting nucleic acid amplification products.

13. Gene site DNA amplification was analyzed with polymerase chain reaction - single strand conformation polymorphism ( PCR - SSCP ).

14. By polymerase chain reaction (PCR), the seasonal variation of the phytoplasmal amounts in mulberry tree was determined.

15. Semi - quantitative reverse transcription - polymerase chain reaction ( RT - PCR ) was used to detect the level of MMP - 12 mRNA expression.

16. Objective To develop a novel multiplex polymerase chain reaction ( PCR ) to detect multidrug - resistant Acinetobacter baumannii.

17. Beta - exotoxin is an inhibitor of RNA polymerase and acts competitively with ATP in various biological processes.

18. Methods Polymerase chain reaction ( PCR ) connected with reverse dot blot ( RDB ) were performed.

19. Suddenly, RNA polymerase is let go,[http:///polymerase.html] raising along the DNA to read the gene.

20. The additional upstream footprint due to wild type RNA polymerase is indicated by the dashed bracket.

21. The discriminating factor between the three promoters appears to be the same for each RNA polymerase.

22. The functional characteristics of these two strong promoters suggest that they are not optimized for a tight and stable RNA polymerase binding.

23. In summary, we have identified two ORFs which encode RNA polymerase subunits with considerable similarity to their cellular counterparts.

24. The more drugs that one gives, the more likely it is that damage to host DNA polymerase will take place.

25. Only one strand of the linkers ligated to the cDNA and the single strand gap was repaired with Taq polymerase prior to amplification.

26. When this was applied to tissue sections, however, most samples were found to inhibit the polymerase chain reaction.

27. Indeed all the signatures of an active ternary complex are lost when these altered enzymes are substituted for wild-type RNA polymerase.

28. A specific semi-nested RT-PCR based on the RNA-dependent RNA polymerase gene in AF469603 of Chinese bee (Apis sinensis) sacbrood virus was established to detect Chinese bee sacbrood virus.

29. Biochip technology is a great breakthrough of life science after recombinant DNA technology and polymerase chain reaction.

30. The sex of embryos were determined with PCR ( Polymerase chain reaction ) technique.

31. Objective : To evaluate multiple seminested polymerase chain reaction ( msn PCR ) in detecting cytomegalovirus ( CMV ) UL 54 gene.

32. Briefly, most mature miRNAs are the products of RNA polymerase II-transcribed transcripts that have been processed by two RNase III enzymes, Drosha and Dicer.

33. ObjectiveTo establish the rapid detection method of Enterotoxigenic E. coli(ETEC)by polymerase chain reaction(PCR)technology for characteristic primers.

34. Objective To evaluate the nested polymerase chain reaction ( NPCR ) technique in diagnosing endobronchial tuberculosis.

35. Objective To find out an ideal method used in identification of Streptococcus sanguis group (SSG) strains by arbitrary primed polymerase chain reaction (AP-PCR).

36. A panel of 24 oral fluids was used to investigate if measles virus haemagglutinin (H) and nucleocapsid (N) genes could be amplified by polymerase chain reaction directly from used POCT strips.

37. A polymerase chain reaction ( PCR ) was developed and evaluated to detect porcine parvovirus ( PPV ).

38. Methods Polymerase chain reaction was used to detect Spotted fever Group Ricketfsiase DNA in tick and rodents spleen.

39. Meanwhile, biochemical reaction, coagglutination test, metabolism-inhibition test, polymerase chain reaction (PCR), and DNA sequence assay were employed to identify those positive cultures.

40. Methods Polymerase chain reaction (PCR) was used to check and measure the tubercle bacillus DNA(TB-DNA) in malignancy tissue.

41. The expression of TLR 4, MD - 2 mRNA were assayed by reverse transcriptase polymerase chain reaction ( RT - PCR ).

42. Methods LOH at APC and MCC genetic loci in 46 specimens resected from esophageal neoplasm was studied with polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP).

43. METHODS:Polymerase chain reaction restriction fragment length polymorphism(PCR RFLP) was used to analyze NQO1 gene polymorphism in Parkinson disease group and healthy adult control group.

44. The RNA polymerase unzips a small portion of the DNA helix exposing the bases on each strand.

45. Preparation and identification of the thermostable DNA polymerase expressed in E.

46. The proto - oncogene c - fos mRNA expression was assessed using reverse transcription polymerase chain reaction ( RT - PCR ).

47. How far along the DNA would the transcription "bubble" formed by RNA polymerase move in 10s?

48. Method: Reverse transcription polymerase chain reaction(RT-PCR) was used to examine the deletions at P16 and FHIT in 52 patients with lung cancer and 9 patients with nonmalignant disease.

49. Methods HBV genotypes were detected by polymerase chain reaction(PCR) and restriction fragment length polymorphism analysis(RFLP) in 136 HBV DNA positive patients who were born in Shanghai.

50. Objective To discuss the feasibility and superiority of diagnosis of acanthamoeba Keratitis using polymerase chain reaction.

51. This study was aimed to establish a ST-based cell line stably expressing the T7 RNA polymerase,[/polymerase.html] which can be used in the reverse genetic manipulation of CSFV and other swine RNA viruses.

52. Current TB drugs known as rifamycins also act on RNA polymerase, but they do it in a different way.

53. Methods: Polymerase chain reaction ( PCR ), DNA direct nucleotide sequencing and RFLP were used in mutation analysis.

54. DNA saturation experiment is a convenient method for measuring the relative amount and specific activity of RNA polymerase.

55. Abstract Object To identify and detect Dermatophagoides farina (D. f) and Dermatophagoides pteronyssinu(D. p)by Polymerase Chain Reaction (PCR) technology.

56. Conclusion The influenza virus RNA polymerase PB1 1 is subcloned and expressed in E. coli successfully.

57. Practice of the patented polymerase chain reaction ( PCR ) process requires a license.

58. We have compared the immunological properties of RNA polymerase B from 615 and L615 mouse livers in double immunodiffusion test.

59. DNA molecule to which RNA polymerase binds, initiating the transcription of messenger RNA.

60. Objective To establish DNA typing for HLA - DR antigens polymerase chain reaction with sequence - specific primers ( PCR - SSP ).

61. There are several methods for sexing embryos, such as karyotype analysis, H-Y antigen detection, X-linked enzymatic determination and polymerase chain reaction (PCR) amplification.

62. Two papers published in Nature describe the structure of a part of RNA polymerase, an important H5N1 virus enzyme that is responsible for virus replication in host cells.

63. Methods We used the polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) to examine 40 oral squamous cell carcinomas for loss of heterozygosity (LOH) at APC.

64. These results suggested that T7 promoter functions as cis-acting elements of RNA polymerase transcriptional system in eucaryotic cells.

65. The TPH gene A218C polymorphism and the MAOA gene T1460C polymorphism were determined by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique.

66. A variety of RNA polymerase containing zinc, while the nuclear of acid reductase action is dependent on iron.

67. Methods:Polymerase chain reaction (PCR) and single strand conformation polymorphism(SSCP) was used.

68. The KOH preparation was consistent with a fungal pathogen, which was later identified as Blastomyces dermatitidis by polymerase chain reaction.

69. Expression of apoptosis - related proteins ( Caspase - 3 , Caspase - 8 and poly ADP - ribose polymerase ( PARP )) was determined by immunohistochemistry.

70. We will also stress the importance of hydrogen bonding, base pair geometry, polymerase DNA interactions and the role of accessory proteins in replication fidelity.

71. As bases are added by polymerase to the starting point of a new complementary strand, known as a primer, or recognized by ligase as a match, the template's sequence is revealed.

72. Biochemical reaction, coagglutination test, metabolism inhibition test, polymerase chain reaction (PCR) assay, and DNA sequencing were employed to identify the isolated microorganisms.

73. "I asked, What's the probability that I would see a human DNA polymerase [protein] sequence and another protein with an E. coli DNA polymerase sequence?" he explained.

74. Methods To illustrate the relationship of H3 subtype influenza virus with other subtypes, we carried out the sequence analysis of PB1 polymerase genes of three H3N8 subtype du.

75. The polymerase chain reaction (PCR) was first conceived by Kerry Mullis, while he was working at Cetus Corporation.

76. In H5N1, perhaps the most important of these proteins is RNA polymerase, which contains the instructions that allows the virus to copy itself along with all of its genetic material.

77. Methods: The animal model was established in composite factors. Animal experiments with enzyme kinetics and PCR(polymerase chain reaction) technique were conducted.

78. Total RNA was isolated and gelatinase A (MMP2) gene expression level were measured by reverse transcription polymerase chain reaction (RT-PCR).

78. is a sentence dictionary, on which you can find excellent sentences for a large number of words.

79. In laboratories, the methods mainly include polymerase chain reaction, restriction fragment length polymorphism, and biochip technology.

80. In laboratories, the methods mainly include polymerase chain reaction, restriction fragment length polymorphism, and biochip technology. The methods mentioned above all have their merits and defects.

81. Conclusion Palmatine and Berberine are inhibitors of DNA polymerase of tumor cells.

82. Multiple allele specific polymerase chain reaction (MASPCR) was used for targeted DNA amplification and gene mutation analysis.

83. This research has optimized the method of extracting the DNA of different parts of papaya and its highly-processed products, therefore successfully extracted the DNA for PCR(polymerase chain reation).

84. The assembled factors include an RNA polymerase, the blue molecule.

85. Methods: Polymerase chain reaction-single strand conformation polymorphism(PCR-SSCP) was used to exclude known gene mutation of HGF from 2 familial gingival fibromatosis .

86. The diagnosis is supported or confirmed by growing the bacteria from specimens of spinal fluid or blood, by agglutination tests or by polymerase chain reaction (PCR).

87. Method Polymerase chain reaction and restriction fragment length polymorphism were used to examine 40 oral malignant tumors for loss of heterozygosity at chromosome 3p.

88. Objective The arbitrarily primed polymerase chain reaction(AP-PCR) was established to identify the common dermatophyte fungi.

89. Methods Reverse transcription - polymerase chain reaction ( RT - PCR ), and immunohistochemical method were used.

90. METHODS:Polymerase chain reaction(PCR) combined with restriction enzyme digest ion were used to detect gene specific junction fragments of the 23 CMT1 patients and 30 normal controls.

91. Navarro and Gull found that the transcriptional body of the parasite uses a less abundant type of enzyme called RNA polymerase I to read the VSG genes.

92. Researchers believe that the bird virus polymerase allows for faster replication, and thus more aggressive.

93. Method The histochemical staining and polymerase chain reaction was used to detect oral leukoplakia.

94. Objective To develop a quantitative real - time polymerase chain reaction ( PCR ) for detecting Bartonella henselae.

95. DNA molecule to RNA polymerase binds, initiating the transcription of RNA.

96. Methods DNAs were extracted from the white blood cells of people in Hainan by salt-out method. Polymerase chain reaction and restriction endonuclease was used to determine the 4533G/A polymorphism.

97. The HBV markers and HBV DNA in poultry sera, Yolk and bovine milk whey were detected by reversed passive hemagglutination assay (RPHA), enzyme immunoassay (EIA) and polymerase chain reaction (PCR).

98. Conclusion The protein, RNA polymerase subunit encoded putatively by the clone, is high conservative in different species.