ライフサイエンスコーパス: transcription product

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1 f IAP transcripts, Gag proteins, and reverse transcription products.

2 ntry, before the generation of viral reverse transcription products.

3 ability of MLV particles to generate reverse transcription products.

4 prising approximately 80% of the total viral transcription products.

5 mate size expected for a full-length reverse transcription product and with plus-strand strong-stop D

6 rastically decreased wild-type HIV-1 reverse transcription products and infectivity.

7 decreased amounts of early and late reverse transcription products and integrated virus relative to

8 xosomes reduce accumulation of HIV-1 reverse transcription products and steady-state levels of HIV-1

9 ing strategy to characterize nascent reverse transcription products and their precise 3'-termini in H

10 , results in reduced accumulation of reverse transcription products, and is dominant in heterokaryons

11 tilize an unspliced version of their primary transcription product as an RNA template for synthesis o

12 em, Transchip, was developed for analysis of transcription products at their genomic origins.

13 is to investigate the length distribution of transcription products at various times following initia

14 The standard is added to the reverse transcription product before PCR.

15 and MDDCs revealed similar levels of reverse transcription products, but increased nuclear import in

16 es by preventing the accumulation of reverse transcription products, but the underlying mechanism rem

17 evealed that the generation of early reverse transcription products coincides with the timing of unco

18 integration, indicating that a viral reverse transcription product comprises the HIV-1 pathogen-assoc

19 ll mutants tested produced levels of reverse transcription products either similar to or only somewha

20 Finally, HIV-1 reverse transcription products escaping rhesus TRIM5alpha restri

21 the normal generation of HIV-1 late reverse transcription products, even though HIV-1 infection and

22 llowing a blood meal, and those accumulating transcription products exclusively or preferentially in

23 after virion entry and prevent viral reverse transcription products from accumulating.

24 how a decreased tendency to produce aberrant transcription products from DNA templates having protrud

25 The quantitative measurement of transcription products from homologous alleles at a dipl

26 e was determined by real-time PCR on reverse transcription products from RNA isolated from human corn

27 to other cytosolic sensors of viral reverse transcription products in newly infected cells.

28 Analysis of reverse transcription products in OMK cells revealed that the ge

29 e conserved exonic IES determine alternative transcription products in the developing macronucleus; s

30 bition, prevents the accumulation of reverse transcription products in the target cell.

31 aggregates promote synthesis of long reverse transcription products in vitro by concentrating nucleic

32 Other classes of reverse transcription products, including some that resulted fro

33 te the synthesis of RNA polymerase (Pol) III transcription products, including tRNAs and 5S rRNAs, wa

34 tive real-time PCR analysis of early reverse transcription products indicated that HIV-1 reverse tran

35 We detected truncated transcription products indicating partial transcription

36 iant was impaired in generating late reverse transcription products, indicating that replication was

37 , and mediate the integration of the reverse-transcription product into the genome of the host cell.

38 The retroviral primary transcription product is a multifunctional RNA that is u

39 multiple ways and that inhibition of reverse transcription products is not necessary for TRIM5-mediat

40 tantially reduced, neither the amount of HBV transcription products nor the core polypeptide was dete

41 lding a short, truncated L mRNA as the major transcription product of the L gene.

42 s oxyR homolog and provide evidence that the transcription product of this gene binds to the B. abort

43 For this study, we examined reverse transcription products of human immunodeficiency virus (

44 that, like p53, p73alpha and the alternative transcription product p73beta also bind MDM2.

45 antitative real-time PCR analysis of reverse transcription products revealed that the mutant RTs were

46 Detailed analyses of the reverse transcription products synthesized within nucleocapsids

47 e, and cell death through an undefined CIITA transcription product that may serve as a new antiviral

48 iency virus type 1 (HIV-1), allowing reverse transcription products to accumulate even though viral i

49 ication, including synthesis of late reverse transcription products, two-long terminal repeat circles

50 ve methods that monitor formation of reverse transcription products, two-LTR circles and integrated p

51 microring resonators to detect cDNA reverse transcription products via a subsequent enzymatic signal

52 Although most of the primary transcription products were multigenomic in length, some

53 However, reverse transcription products were substantially increased in t

54 indicate that faithful, full-length reverse transcription products were underrepresented in the abse

55 ction and quantitative PCR for HIV-1 reverse transcription products, whereas treatment of the target

56 tive real-time PCR analysis of early reverse transcription products, with initiation at the HIV-1 PBS

57 thesis.IMPORTANCE The fates of HIV-1 reverse transcription products within infected cells are not wel

58 r viral DNA as well as intracellular reverse transcription products, without affecting HBV RNAs or cc

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