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Thermo Fisher gene exp pde4b rn00566785 m1
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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MedChemExpress pde4b kd rs09 group
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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Advanced Cell Diagnostics Inc rnascope probe mm-pde4b-c1
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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Biorbyt rabbit anti rat pde4b
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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Biorbyt pde4b
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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Shanghai GenePharma sirna targeting pde4b
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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Pfizer Inc pde4b-targeted pet probe [ 18 f]pf-06445974
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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MyBiosource Biotechnology pde4b/c/d antibody
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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GeneTex pde4b antibody
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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Tocris selective pde4b inhibitor a33
In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( <t>Pde4b</t> ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).
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In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( Pde4b ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).

Journal: Experimental neurology

Article Title: Daily acute intermittent hypoxia elicits age & sex-dependent changes in molecules regulating phrenic motor plasticity

doi: 10.1016/j.expneurol.2025.115240

Figure Lengend Snippet: In young males, dAIH exposure significantly reduced Q pathway associated 5HT2A receptor expression (Panel A). In young females, dAIH significantly reduced S to Q cross talk molecules – p38Map kinase β ( Mapk11 ) and phosphodiesterase ( Pde4b ) expression. Reduced phosphodiesterase expression could indirectly increase PKA or EPAC activity which could in turn increase S to Q inhibition (Panel B). In middle aged males, no significant effect of dAIH exposure was observed (Panel C). In contrast widespread gene expression changes with dAIH exposure were observed in middle aged females. dAIH reduced expression of 5HT2B and A2A receptor, Q to S cross talk molecules–PKCδ ( Prkcd ) and NADPH-p47 ( Ncf1 ), S to Q cross-talk molecules phosphodiesterase 4b, and fractalkine ( Cx3cl1 ) (Panel D).

Article Snippet: phosphodiesterase 4B , pde4b , S to Q crosstalk , Rn00566785_m1 , 70.

Techniques: Expressing, Activity Assay, Inhibition, Gene Expression