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Items: 1 to 20 of 80

1.

Amygdalar glutamatergic neuronal systems play a key role on the hibernating state of hamsters.

Alò R, Avolio E, Carelli A, Facciolo RM, Canonaco M.

BMC Neurosci. 2011 Jan 20;12:10. doi: 10.1186/1471-2202-12-10.

2.

Amygdalar excitatory/inhibitory circuits interacting with orexinergic neurons influence differentially feeding behaviors in hamsters.

Avolio E, Alò R, Mele M, Carelli A, Canonaco A, Bucarelli L, Canonaco M.

Behav Brain Res. 2012 Sep 1;234(1):91-9. doi: 10.1016/j.bbr.2012.06.013. Epub 2012 Jun 20.

PMID:
22728307
3.

Excitatory/inhibitory equilibrium of the central amygdala nucleus gates anti-depressive and anxiolytic states in the hamster.

Alò R, Avolio E, Mele M, Storino F, Canonaco A, Carelli A, Canonaco M.

Pharmacol Biochem Behav. 2014 Mar;118:79-86. doi: 10.1016/j.pbb.2014.01.007. Epub 2014 Jan 24.

PMID:
24468014
4.

Distinct α subunit variations of the hypothalamic GABAA receptor triplets (αβγ) are linked to hibernating state in hamsters.

Alò R, Avolio E, Di Vito A, Carelli A, Facciolo RM, Canonaco M.

BMC Neurosci. 2010 Sep 6;11:111. doi: 10.1186/1471-2202-11-111.

6.

Amygdalar orexinergic-GABAergic interactions regulate anxiety behaviors of the Syrian golden hamster.

Avolio E, Alò R, Carelli A, Canonaco M.

Behav Brain Res. 2011 Apr 15;218(2):288-95. doi: 10.1016/j.bbr.2010.11.014. Epub 2010 Nov 11.

PMID:
21074570
7.
8.

Contribution of AMPA and NMDA receptors to excitatory responses in the inferior colliculus.

Kelly JB, Zhang H.

Hear Res. 2002 Jun;168(1-2):35-42. Review.

PMID:
12117507
9.
10.

Catestatin and orexin-A neuronal signals alter feeding habits in relation to hibernating states.

Mele M, Avolio E, Alò R, Fazzari G, Mahata SK, Canonaco M.

Neuroscience. 2014 Jun 6;269:331-42. doi: 10.1016/j.neuroscience.2014.03.065. Epub 2014 Apr 8.

PMID:
24721733
11.

Expression variations of chromogranin A and α1,2,4 GABA(A)Rs in discrete limbic and brainstem areas rescue cardiovascular alterations.

Avolio E, Facciolo RM, Alò R, Mele M, Carelli A, Canonaco A, Mosciaro L, Talani G, Biggio G, Sanna E, Mahata SK, Canonaco M.

Neurosci Res. 2013 Sep-Oct;77(1-2):8-15. doi: 10.1016/j.neures.2013.07.006. Epub 2013 Aug 3.

PMID:
23916832
12.

Xenon reduces N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor-mediated synaptic transmission in the amygdala.

Haseneder R, Kratzer S, Kochs E, Eckle VS, Zieglgänsberger W, Rammes G.

Anesthesiology. 2008 Dec;109(6):998-1006. doi: 10.1097/ALN.0b013e31818d6aee.

PMID:
19034096
13.

Are NMDA or AMPA/kainate receptor antagonists more efficacious in the delayed treatment of excitotoxic neuronal injury?

Prehn JH, Lippert K, Krieglstein J.

Eur J Pharmacol. 1995 Jan 13;292(2):179-89.

PMID:
7720791
14.

Brain excitatory/inhibitory circuits cross-talking with chromogranin A during hypertensive and hibernating states.

Giusi G, Alò R, Avolio E, Zizza M, Facciolo RM, Talani G, Biggio G, Sanna E, Canonaco M.

Curr Med Chem. 2012;19(24):4093-114. Review.

PMID:
22834800
16.

Bcl-2/Bax expression levels tend to influence AMPAergic trafficking mechanisms during hibernation in Mesocricetus auratus.

Mele M, Alò R, Avolio E, Canonaco M.

J Mol Neurosci. 2015 Feb;55(2):374-84. doi: 10.1007/s12031-014-0342-3. Epub 2014 Jun 1.

PMID:
24880241
18.
20.

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