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Dorsal hippocampus ERK2 signaling mediates anxiolytic-related behavior in male rats

Louis Stokes Alliances for Minority Participation AND Program Evaluation

Parise LF, Sierra-Fonseca JA.
GSID: Hv0blVngq_MJ
JA Sierra-Fonseca, LF Parise… - Chronic …, 2019 - journals.sagepub.com

Background Anxiety disorders are the most common neuropathologies worldwide, but the precise neuronal mechanisms that underlie these disorders remain unknown. The hippocampus plays a role in mediating anxiety-related responses, which can be modeled in rodents using behavioral assays, such...

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Sierra-Fonseca, J. A., Parise, L. F., Flores-Ramirez, F. J., Robles, E. H., Garcia-Carachure, I., & Iñiguez, S. D. (2019). Dorsal hippocampus ERK2 signaling mediates anxiolytic-related behavior in male rats. Chronic stress, 3, 2470547019897030.
Sierra-Fonseca, Jorge A., et al. "Dorsal hippocampus ERK2 signaling mediates anxiolytic-related behavior in male rats." Chronic stress 3 (2019): 2470547019897030.
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A take-home physics experiment kit for on-campus and off-campus students

science campus

Turner J, Parisi A.
GSID: Q_ypQb9F5rwJ
J Turner, A Parisi - Teaching Science, 2008 - search.informit.org

A take-home experiment kit has been developed to reinforce the concepts in a first year physics course that both on and off campus students from a variety of educational backgrounds can successfully use. The kit is inexpensive and is...

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Turner, J., & Parisi, A. (2008). A take-home physics experiment kit for on-campus and off-campus students. Teaching Science, 54(2), 20-23.
Turner, Joanna, and Alfio Parisi. "A take-home physics experiment kit for on-campus and off-campus students." Teaching Science 54.2 (2008): 20-23.
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Validation of Ozone Monitoring Instrument UV Satellite Data Using Spectral and Broadband Surface Based Measurements at a Queensland Site.

Photochemistry and photobiology

A Jebar MA, Parisi AV, Downs NJ, Turner JF.
PMID: 28449224
Photochem Photobiol. 2017 Oct;93(5):1289-1293. doi: 10.1111/php.12784. Epub 2017 Jul 27.

This research reconstructed and validated the broadband UVA irradiances derived from discrete spectral irradiance data retrieved from the Ozone Monitoring Instrument (OMI) satellite from 1 January to 31 December 2009. OMI data at solar noon were compared to ground-based...

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A Jebar MA, Parisi AV, Downs NJ, et al. Validation of Ozone Monitoring Instrument UV Satellite Data Using Spectral and Broadband Surface Based Measurements at a Queensland Site. Photochem Photobiol. 2017;93(5):1289-1293doi: 10.1111/php.12784.
A Jebar, M. A., Parisi, A. V., Downs, N. J., & Turner, J. F. (2017). Validation of Ozone Monitoring Instrument UV Satellite Data Using Spectral and Broadband Surface Based Measurements at a Queensland Site. Photochemistry and photobiology, 93(5), 1289-1293. https://doi.org/10.1111/php.12784
A Jebar, Mustapha A, et al. "Validation of Ozone Monitoring Instrument UV Satellite Data Using Spectral and Broadband Surface Based Measurements at a Queensland Site." Photochemistry and photobiology vol. 93,5 (2017): 1289-1293. doi: https://doi.org/10.1111/php.12784
A Jebar MA, Parisi AV, Downs NJ, Turner JF. Validation of Ozone Monitoring Instrument UV Satellite Data Using Spectral and Broadband Surface Based Measurements at a Queensland Site. Photochem Photobiol. 2017 Oct;93(5):1289-1293. doi: 10.1111/php.12784. Epub 2017 Jul 27. PMID: 28449224.
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Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers.

The Journal of organic chemistry

Arnaud-Neu F, Caccamese S, Fuangswasdi S, Pappalardo S, Parisi MF, Petringa A, Principato G.
PMID: 11671909
J Org Chem. 1997 Nov 14;62(23):8041-8048. doi: 10.1021/jo970934e.

Reaction of mono-O-alkylated calix[4]arenes 2 with tri- to pentaethylene glycol ditosylates and K(2)CO(3) affords asymmetrical (1,2)-calix[4]crown ether derivatives 3 as the main product, along with minor amounts of calix[4]arene dimers 4 and mixed syn-distal di-O-alkylated calix[4]arenes 5. A reaction...

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Arnaud-Neu F, Caccamese S, Fuangswasdi S, et al. Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers. J Org Chem. 1997;62(23):8041-8048doi: 10.1021/jo970934e.
Arnaud-Neu, F., Caccamese, S., Fuangswasdi, S., Pappalardo, S., Parisi, M. F., Petringa, A., & Principato, G. (1997). Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers. The Journal of organic chemistry, 62(23), 8041-8048. https://doi.org/10.1021/jo970934e
Arnaud-Neu, Francoise, et al. "Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers." The Journal of organic chemistry vol. 62,23 (1997): 8041-8048. doi: https://doi.org/10.1021/jo970934e
Arnaud-Neu F, Caccamese S, Fuangswasdi S, Pappalardo S, Parisi MF, Petringa A, Principato G. Synthesis, Optical Resolution and Complexation Properties of Inherently Chiral Monoalkylated p-tert-Butyl-(1,2)-calix[4]crown Ethers. J Org Chem. 1997 Nov 14;62(23):8041-8048. doi: 10.1021/jo970934e. PMID: 11671909.
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Interfacial electron transfer in FeII(CN)6 4- -sensitized TiO2 nanoparticles: a study of direct charge injection by electroabsorption spectroscopy.

Journal of the American Chemical Society

Khoudiakov M, Parise AR, Brunschwig BS.
PMID: 12683836
J Am Chem Soc. 2003 Apr 16;125(15):4637-42. doi: 10.1021/ja0299607.

Electroabsorption (Stark) spectroscopy has been used to study the dye sensitized interfacial electron transfer in an Fe(II)(CN)(6)(4)(-) donor complex bound to a TiO(2) nanoparticle. The average charge-transfer distance determined from the Stark spectra is 5.3 A. This value is...

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Khoudiakov M, Parise AR, Brunschwig BS. Interfacial electron transfer in FeII(CN)6 4- -sensitized TiO2 nanoparticles: a study of direct charge injection by electroabsorption spectroscopy. J Am Chem Soc. 2003;125(15):4637-42doi: 10.1021/ja0299607.
Khoudiakov, M., Parise, A. R., & Brunschwig, B. S. (2003). Interfacial electron transfer in FeII(CN)6 4- -sensitized TiO2 nanoparticles: a study of direct charge injection by electroabsorption spectroscopy. Journal of the American Chemical Society, 125(15), 4637-42. https://doi.org/10.1021/ja0299607
Khoudiakov, Mikhail, et al. "Interfacial electron transfer in FeII(CN)6 4- -sensitized TiO2 nanoparticles: a study of direct charge injection by electroabsorption spectroscopy." Journal of the American Chemical Society vol. 125,15 (2003): 4637-42. doi: https://doi.org/10.1021/ja0299607
Khoudiakov M, Parise AR, Brunschwig BS. Interfacial electron transfer in FeII(CN)6 4- -sensitized TiO2 nanoparticles: a study of direct charge injection by electroabsorption spectroscopy. J Am Chem Soc. 2003 Apr 16;125(15):4637-42. doi: 10.1021/ja0299607. PMID: 12683836.
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Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation.

The Journal of organic chemistry

De Salvo G, Gattuso G, Notti A, Parisi MF, Pappalardo S.
PMID: 11856007
J Org Chem. 2002 Feb 08;67(3):684-92. doi: 10.1021/jo015982k.

A series of tri-O-substituted 1,3-bridged calix[5]arene crown-6 ethers bearing alkyl, arylalkyl, alkoxyalkyl, and alkoxycarbonylmethyl residues at the lower rim and either (t)()Bu or H substituents at the upper rim have been synthesized. (1)H NMR studies have shown that p-tert-butylcalix[5]crowns,...

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De Salvo G, Gattuso G, Notti A, et al. Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation. J Org Chem. 2002;67(3):684-92doi: 10.1021/jo015982k.
De Salvo, G., Gattuso, G., Notti, A., Parisi, M. F., & Pappalardo, S. (2002). Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation. The Journal of organic chemistry, 67(3), 684-92. https://doi.org/10.1021/jo015982k
De Salvo, Gabriella, et al. "Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation." The Journal of organic chemistry vol. 67,3 (2002): 684-92. doi: https://doi.org/10.1021/jo015982k
De Salvo G, Gattuso G, Notti A, Parisi MF, Pappalardo S. Shape recognition of alkylammonium ions by 1,3-bridged calix[5]arene crown-6 ethers: endo- vs exo-cavity complexation. J Org Chem. 2002 Feb 08;67(3):684-92. doi: 10.1021/jo015982k. PMID: 11856007.
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Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach.

Chemical communications (Cambridge, England)

D'Urso A, Nicotra PF, Centonze G, Fragalà ME, Gattuso G, Notti A, Pappalardo A, Pappalardo S, Parisi MF, Purrello R.
PMID: 22430063
Chem Commun (Camb). 2012 Apr 28;48(34):4046-8. doi: 10.1039/c2cc30366c. Epub 2012 Mar 20.

CD and UV-vis measurements were carried out to demonstrate chirality induction-promoted by chiral covalently linked groups and non-covalently bound Δ- and Λ-[Ru(phen)(3)](2+) enantiomers-in metallo-porphyrin-calixarene and metallo-porphyrin-bis-calixarene non-covalent assemblies, respectively.

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D'Urso A, Nicotra PF, Centonze G, et al. Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach. Chem Commun (Camb). 2012;48(34):4046-8doi: 10.1039/c2cc30366c.
D'Urso, A., Nicotra, P. F., Centonze, G., Fragalà, M. E., Gattuso, G., Notti, A., Pappalardo, A., Pappalardo, S., Parisi, M. F., & Purrello, R. (2012). Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach. Chemical communications (Cambridge, England), 48(34), 4046-8. https://doi.org/10.1039/c2cc30366c
D'Urso, Alessandro, et al. "Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach." Chemical communications (Cambridge, England) vol. 48,34 (2012): 4046-8. doi: https://doi.org/10.1039/c2cc30366c
D'Urso A, Nicotra PF, Centonze G, Fragalà ME, Gattuso G, Notti A, Pappalardo A, Pappalardo S, Parisi MF, Purrello R. Induction of chirality in porphyrin-(bis)calixarene assemblies: a mixed covalent-non-covalent vs a fully non-covalent approach. Chem Commun (Camb). 2012 Apr 28;48(34):4046-8. doi: 10.1039/c2cc30366c. Epub 2012 Mar 20. PMID: 22430063.
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Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors.

BMC clinical pathology

Aziz SA, Sznol JA, Adeniran A, Parisi F, Kluger Y, Camp RL, Kluger HM.
PMID: 23374878
BMC Clin Pathol. 2013 Feb 01;13:3. doi: 10.1186/1472-6890-13-3.

BACKGROUND: Targeted therapies in renal cell carcinoma can have different effects on primary and metastatic tumors. To pave the way for predictive biomarker development, we assessed differences in expression of targets of currently approved drugs in matched primary and...

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Aziz SA, Sznol JA, Adeniran A, et al. Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors. BMC Clin Pathol. 2013;13:3doi: 10.1186/1472-6890-13-3.
Aziz, S. A., Sznol, J. A., Adeniran, A., Parisi, F., Kluger, Y., Camp, R. L., & Kluger, H. M. (2013). Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors. BMC clinical pathology, 133. https://doi.org/10.1186/1472-6890-13-3
Aziz, Saadia A, et al. "Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors." BMC clinical pathology vol. 13 (2013): 3. doi: https://doi.org/10.1186/1472-6890-13-3
Aziz SA, Sznol JA, Adeniran A, Parisi F, Kluger Y, Camp RL, Kluger HM. Expression of drug targets in primary and matched metastatic renal cell carcinoma tumors. BMC Clin Pathol. 2013 Feb 01;13:3. doi: 10.1186/1472-6890-13-3. PMID: 23374878; PMCID: PMC3575219.
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Histologic coagulative tumour necrosis as a prognostic indicator of aggressiveness in renal, lung, thyroid and colorectal carcinomas: A brief review.

Oncology letters

Caruso R, Parisi A, Bonanno A, Paparo D, Quattrocchi E, Branca G, Scardigno M, Fedele F.
PMID: 22740848
Oncol Lett. 2012 Jan;3(1):16-18. doi: 10.3892/ol.2011.420. Epub 2011 Sep 16.

Tumour growth involves two essential deviations from the normal state including the induction of proliferative stimuli, and simultaneous suppression of potentially compensatory cell death. It has been suggested that the development of invasive cancer involves a progressive switch from...

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Caruso R, Parisi A, Bonanno A, et al. Histologic coagulative tumour necrosis as a prognostic indicator of aggressiveness in renal, lung, thyroid and colorectal carcinomas: A brief review. Oncol Lett. 2011;3(1):16-18doi: 10.3892/ol.2011.420.
Caruso, R., Parisi, A., Bonanno, A., Paparo, D., Quattrocchi, E., Branca, G., Scardigno, M., & Fedele, F. (2012). Histologic coagulative tumour necrosis as a prognostic indicator of aggressiveness in renal, lung, thyroid and colorectal carcinomas: A brief review. Oncology letters, 3(1), 16-18. https://doi.org/10.3892/ol.2011.420
Caruso, Rosario, et al. "Histologic coagulative tumour necrosis as a prognostic indicator of aggressiveness in renal, lung, thyroid and colorectal carcinomas: A brief review." Oncology letters vol. 3,1 (2012): 16-18. doi: https://doi.org/10.3892/ol.2011.420
Caruso R, Parisi A, Bonanno A, Paparo D, Quattrocchi E, Branca G, Scardigno M, Fedele F. Histologic coagulative tumour necrosis as a prognostic indicator of aggressiveness in renal, lung, thyroid and colorectal carcinomas: A brief review. Oncol Lett. 2012 Jan;3(1):16-18. doi: 10.3892/ol.2011.420. Epub 2011 Sep 16. PMID: 22740848; PMCID: PMC3362430.
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Anion-assisted supramolecular polymerization: from achiral AB-type monomers to chiral assemblies.

Angewandte Chemie (International ed. in English)

Capici C, Cohen Y, D'Urso A, Gattuso G, Notti A, Pappalardo A, Pappalardo S, Parisi MF, Purrello R, Slovak S, Villari V.
PMID: 21998004
Angew Chem Int Ed Engl. 2011 Dec 09;50(50):11956-61. doi: 10.1002/anie.201104357. Epub 2011 Oct 13.

No abstract available.

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Capici C, Cohen Y, D'Urso A, et al. Anion-assisted supramolecular polymerization: from achiral AB-type monomers to chiral assemblies. Angew Chem Int Ed Engl. 2011;50(50):11956-61doi: 10.1002/anie.201104357.
Capici, C., Cohen, Y., D'Urso, A., Gattuso, G., Notti, A., Pappalardo, A., Pappalardo, S., Parisi, M. F., Purrello, R., Slovak, S., & Villari, V. (2011). Anion-assisted supramolecular polymerization: from achiral AB-type monomers to chiral assemblies. Angewandte Chemie (International ed. in English), 50(50), 11956-61. https://doi.org/10.1002/anie.201104357
Capici, Calogero, et al. "Anion-assisted supramolecular polymerization: from achiral AB-type monomers to chiral assemblies." Angewandte Chemie (International ed. in English) vol. 50,50 (2011): 11956-61. doi: https://doi.org/10.1002/anie.201104357
Capici C, Cohen Y, D'Urso A, Gattuso G, Notti A, Pappalardo A, Pappalardo S, Parisi MF, Purrello R, Slovak S, Villari V. Anion-assisted supramolecular polymerization: from achiral AB-type monomers to chiral assemblies. Angew Chem Int Ed Engl. 2011 Dec 09;50(50):11956-61. doi: 10.1002/anie.201104357. Epub 2011 Oct 13. PMID: 21998004.
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Role of ruthenium oxidation states in ligand-to-ligand charge transfer processes.

Inorganic chemistry

Ramírez CL, Pegoraro CN, Filevich O, Bruttomeso A, Etchenique R, Parise AR.
PMID: 22224412
Inorg Chem. 2012 Feb 06;51(3):1261-8. doi: 10.1021/ic200966f. Epub 2012 Jan 06.

We describe in this paper the properties of [Ru(II/III)(bpy)(2)ClL](+1/+2) and [Ru(II/III)(bpy)(2)L(2)](+2/+3). L = ditolyl-3-pyridylamine (dt3pya) is a redox active ligand related to triarylamines, which is very similar to 3-aminopyridine except for the reversible redox behavior. The monosubstituted complex shows...

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Ramírez CL, Pegoraro CN, Filevich O, et al. Role of ruthenium oxidation states in ligand-to-ligand charge transfer processes. Inorg Chem. 2012;51(3):1261-8doi: 10.1021/ic200966f.
Ramírez, C. L., Pegoraro, C. N., Filevich, O., Bruttomeso, A., Etchenique, R., & Parise, A. R. (2012). Role of ruthenium oxidation states in ligand-to-ligand charge transfer processes. Inorganic chemistry, 51(3), 1261-8. https://doi.org/10.1021/ic200966f
Ramírez, Cristina L, et al. "Role of ruthenium oxidation states in ligand-to-ligand charge transfer processes." Inorganic chemistry vol. 51,3 (2012): 1261-8. doi: https://doi.org/10.1021/ic200966f
Ramírez CL, Pegoraro CN, Filevich O, Bruttomeso A, Etchenique R, Parise AR. Role of ruthenium oxidation states in ligand-to-ligand charge transfer processes. Inorg Chem. 2012 Feb 06;51(3):1261-8. doi: 10.1021/ic200966f. Epub 2012 Jan 06. PMID: 22224412.
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The future of medicine--are you prepared?.

American journal of orthopedics (Belle Mead, N.J.)

Parisi DM.
PMID: 24078951
Am J Orthop (Belle Mead NJ). 2013 Aug;42(8):350-1.

No abstract available.

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Parisi DM. The future of medicine--are you prepared?. Am J Orthop (Belle Mead NJ). 2013;42(8):350-1
Parisi, D. M. (2013). The future of medicine--are you prepared?. American journal of orthopedics (Belle Mead, N.J.), 42(8), 350-1.
Parisi, Debra M. "The future of medicine--are you prepared?." American journal of orthopedics (Belle Mead, N.J.) vol. 42,8 (2013): 350-1.
Parisi DM. The future of medicine--are you prepared?. Am J Orthop (Belle Mead NJ). 2013 Aug;42(8):350-1. PMID: 24078951.
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Showing 1 to 12 of 341 entries