ライフサイエンスコーパス: tat gene

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1 cts associated with the lack of a functional tat gene.

2 sity for the sicker child, especially in the tat gene.

3 he wild-type Tat gene or the attenuated H13L Tat gene.

4 lin M (IgM) and human immunodeficiency virus tat genes.

5 l clones transfected with either full-length tat gene (101 amino acids), or in control cells containi

6 human immunodeficiency virus type 1 (HIV-1) Tat gene, a potent transactivator of viral and cellular

7 tion of a T cell line, H9 cells with the HIV-tat gene also resulted in an activation of JNK that was

8 licing of a substrate derived from the HIV-1 tat gene and have shown that hnRNP H family members are

9 Expression of the tat gene as RSV-tat but not that of the CAT gene as RSV-

10 ds to selective transcription of the nef and tat genes before integration.

11 now demonstrate that the requirement for the tat gene can be offset by placing constitutive promoters

12 se transcription seen with HIV-1 lacking the tat gene could not be complemented when the target cells

13 cell lines that contained a provirus with a tat gene deletion (Deltatat).

14 JDV contains a tat gene, encoded by two exons, which has potent transac

15 The region of the tat gene encoding this epitope falls within a region of

16 ychlor inhibited cortisol-stimulated Arg and TAT gene expression.

17 The trans-activator of transcription or TAT gene from HIV-1 encodes a protein that increases the

18 determined that three of the four identified tat genes in Haloferax volcanii are essential for viabil

19 ing transfection of wild-type but not mutant tat genes into cell lines producing HIV-1 lacking tat, t

20 The tat gene of HIV-1 induces the expression of HRES-1/Rab4,

21 taken to investigate the effect of the HIV-1 tat gene on the expression of inducible nitric-oxide syn

22 uorescent reporters and either the wild-type Tat gene or the attenuated H13L Tat gene.

23 uman immunodeficiency virus, type 1 (HIV-1), tat gene stimulates transcriptional activity of the HRES

24 were obtained so that the abilities of these tat genes to stimulate HIV-1 gene expression and reverse

25 ation-defective herpes simplex virus (HSV)-1 tat gene transfer vector, dSTat, was used to transiently

26 eral transgenic mouse lines that express the Tat gene under the control of an actin promoter.

27 HIV, a stable chimeric HIV carrying the JDV tat gene was generated.

28 HIV-1 virions deleted in the tat gene were unable to initiate reverse transcription e

29 n the lentiviral vectors carry an attenuated Tat gene with the H13L mutation.

30 tat genes with mutations in the amino terminus did not s

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