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