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1 The amplicon from this reaction was amplified with a second primer pair.

2 lcer, and 19 chronic gastritis patients) and was amplified with a set of eight microsatellite markers

3 ed aneuploid and corresponding normal tissue were amplified with a degenerate 15mer primer.

4 sensitive force sensor whose force response is amplified with an increase in its arm lengths, demons

5 cases, the effects of fields on spike timing are amplified with decreasing synaptic input slope and i

6 Skate hepatocyte cDNA was amplified with degenerate oligonucleotide probes des

7 ESTs), and for three Pto-like sequences that were amplified with degenerate primers.

8 No such targeted product was amplified with DNA from Trichomonas tenax, Trichomon

9 The 16S rDNA V3 region was amplified with eubacterial primers, and the amplific

10 Of 28 samples, all could be amplified with gp41 primers but only 17 (60.7%) could

11 r effective summation, whereas distal inputs are amplified with high gain and integrated over broader

12 andard conditions, we show that this DNA may be amplified with high efficiency and greater than 99.9%

13 detected, suggesting that the viral DNAs had been amplified with high fidelity.

14 gp41-based HMA for which the target sequence is amplified with highly conserved gp41 primers, known t

15 e a contextual role in appetite control that is amplified with hypocaloric conditioning.

16 al effects of intraarterial infusion of MSCs are amplified with intravenous injection of mannitol.

17 Individual FBN1 exons were amplified with intron-based exon-specific primers;

18 ngly, rhythms in the nucleus accumbens (NAc) were amplified with no changes seen in the prefrontal co

19 Genomic DNAs were amplified with PCR, and the amplified products were

20 The DNA was amplified with primer pairs covering hypervariable r

21 gene from H. pylori-like bacteria could not be amplified with primers for either "H. heilmannii" or

22 ion and only form early transcripts that can be amplified with primers for the R/U5 region.

23 rom a virus with a unique serotype could not be amplified with primers that amplified DNA from all ot

24 Affected male DNA was amplified with primers specific for the retinoschisi

25 utomated instrument platform in which probes are amplified with Q-beta replicase.

26 eted to the IGHJ segments, but only some can be amplified with regular polymerase chain reaction (PCR

27 fferent methods, and 16S rRNA gene fragments were amplified with several different primer pairs prior

28 cycling conditions enabled all genotypes to be amplified with similar efficiency.

29 HCV genotypes 1 to 4 were amplified with similar efficiencies with the ASR.

30 RNA extracted from these cells was amplified with T7 RNA polymerase and used to hybridi

31 with gp41 primers but only 17 (60.7%) could be amplified with the standard C2V5 primers.

32 e complementary deoxyribonucleic acid (cDNA) was amplified with the polymerase chain reaction (PCR) f

33 cellulare identified by conventional methods were amplified with the MYCOB as well as the MAV and MIN

34 All exons of hMLH1 and hMSH2 were amplified with the PCR and screened by using single

35 HNMT phenotypes, and exons of the HNMT gene were amplified with the polymerase chain reaction.

36 ed stool, a 400-bp fragment of C. parvum DNA was amplified with two 26-mer outer primers.

37 After DNA extraction, a 367-bp fragment was amplified with two outer primers.

38 f 433 bp representing nucleotides 319 to 751 was amplified with universal primers.

39 ividual colonies from the subtracted library were amplified with vector-specific primers and arrayed

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