ライフサイエンスコーパス: hnRNA

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1 Cortisol decreased IGFBP-5 hnRNA, the rate of IGFBP-5 transcription, and the activi

2 yrimidine tract binding protein (PTB) and an hnRNA binding protein, heterogeneous nuclear ribonucleop

3 ation of heterogeneous nuclear (hn) RNA, and hnRNA processing.

4 AVP hnRNA and c-fos mRNA in the PVN were also significantly

5 AVP hnRNA did not change significantly in either the parvoce

6 c-fos mRNA, Fos protein, CRF hnRNA, and AVP hnRNA.

7 y contrast, intact rats showed a delayed AVP hnRNA response (peak at 2 hr), the timing of which was m

8 f CRH heterogeneous nuclear RNA (hnRNA), AVP hnRNA and c-fos as a measure of gene transcription and c

9 in c-fos mRNA and Fos protein, increased AVP hnRNA, and caused no detectable change in CRF hnRNA.

10 licited marked increases in both CRH and AVP hnRNAs within the parvocellular division of the nucleus.

11 d upregulation of arginine vasopressin (AVP) hnRNA (120 min).

12 able, increase in arginine vasopressin (AVP) hnRNA in this same compartment.

13 e data indicate that robust increases in CRF hnRNA are closely linked to full expression of c-fos mRN

14 nRNA, and caused no detectable change in CRF hnRNA.

15 s with a time course parallel to that of CRF hnRNA expression.

16 In response to stress, the kinetics of CRF hnRNA responses of intact and ADX rats replaced with low

17 nt increases in c-fos mRNA, Fos protein, CRF hnRNA, and AVP hnRNA.

18 opin-releasing factor heteronuclear RNA (CRF hnRNA; peak at 5 min) and by a delayed upregulation of a

19 CRH hnRNA levels at 120 min in the PVN, amygdala, cingulate

20 To determine if the increases in CRH hnRNA translated to increased CRH peptide, immunocytoche

21 Elevations in CRH hnRNA were also identified in hippocampus, the lateral b

22 The pattern of CRH hnRNA and mRNA responses were similar, decreasing with i

23 In the PVN, CRH hnRNA levels were increased by KA treatment at 15, 60, a

24 MMP13 mRNA expression is mirrored by nascent hnRNA transcription.

25 ltiple levels after the initial synthesis of hnRNA.

26 The number of cells expressing oxytocin hnRNA did not change during pregnancy but increased duri

27 e in the number of cells expressing oxytocin hnRNA, and increased expression is sustained in lactatio

28 In contrast, DHTP did not affect PPE hnRNA, but inhibited the c-fos mRNA response to novelty.

29 d that novelty or HSI elevated levels of PPE hnRNA and c-fos mRNA in the PVN.

30 Estrogen attenuated the elevation of PPE hnRNA in the PVN following HSI, and enhanced the c-fos m

31 decrements in PPG mRNA and increments in PPG hnRNA.

32 rginine vasopressin (AVP) heteronuclear RNA (hnRNA) expression in rats that were intact or adrenalect

33 s increased levels of PPG heteronuclear RNA (hnRNA) in a glucocorticoid-dependent manner, suggesting

34 essin (AVP) messenger and heteronuclear RNA (hnRNA).

35 enkephalin (PPE) mRNA and heteronuclear RNA (hnRNA, primary transcript).

36 o changes in DMT1 heterogeneous nuclear RNA (hnRNA) levels following Mn exposure.

37 anscription using heterogeneous nuclear RNA (hnRNA) showed that insulin suppressed CYP2E1 transcripti

38 y associated with heterogeneous nuclear RNA (hnRNA) within eukaryotic nuclei.

39 induction of CRH heterogeneous nuclear RNA (hnRNA), AVP hnRNA and c-fos as a measure of gene transcr

40 H mRNA precursor (heterogeneous nuclear RNA [hnRNA]) was detected in total RNA from IFN-gamma-treated

41 imary transcript (heterogeneous nuclear RNA, hnRNA) of the oxytocin gene was measured using a 3H-cDNA

42 induction of CRF and AVP heteronuclear RNAs (hnRNAs).

43 Autoradiographs of the SON showed the hnRNA as discrete clumps of silver grains within the nuc

44 Constitutive levels of VP hnRNA levels were very low in the pPVN, but high in the

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