Resiniferatossina (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Resiniferatossina" in Italian language version.

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asahq.org

anesthesiology.pubs.asahq.org

National Institutes of Health, Clinical Center Department of Perioperative Medicine Chemical from cactus-like plant shows promise in controlling surgical pain, while leaving touch and coordination intact, rat study shows News release December 21, 2017, retrieved 28 February 2018.

books.google.com

Pamela Ellsworth e Alan J. Wein, Questions and Answers about Overactive Bladder, Jones & Bartlett Learning, 2009, pp. 97-100, ISBN 978-1-4496-3113-0.

botanical-dermatology-database.info

Euphorbia poissonii in BoDD – Botanical Dermatology Database

doi.org

dx.doi.org

Christopher S. J. Walpole, Similarities and Differences in the Structure-Activity Relationships of Capsaicin and Resiniferatoxin Analogues, in J. Med. Chem., vol. 39, n. 15, 1996, pp. 2939-2952, DOI:10.1021/jm960139d, PMID 8709128.
Szallasi A, Blumberg PM, Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analogue of capsaicin, the irritant constituent in red pepper, in Neuroscience, vol. 30, n. 2, 1989, pp. 515-520, DOI:10.1016/0306-4522(89)90269-8, PMID 2747924.
Szallasi A, Blumberg PM, Resiniferatoxin and its analogues provide novel insights into the pharmacology of the vanilloid (capsaicin) receptor, in Life Sci., vol. 47, n. 16, 1990, pp. 1399-1408, DOI:10.1016/0024-3205(90)90518-V, PMID 2174484.
Szallasi A, Blumberg PM, Vanilloid receptor loss in rat sensory ganglia associated with long term desensitization to resiniferatoxin, in Neurosci. Lett., vol. 140, n. 1, 1992, pp. 51-54, DOI:10.1016/0304-3940(92)90679-2, PMID 1407700.
Olah Z, etal, Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1, in J. Biol. Chem., vol. 276, n. 14, 2001, pp. 11021-11030, DOI:10.1074/jbc.M008392200, PMID 11124944.
Nair AB, Jacob S, A simple practice guide for dose conversion between animals and human, in J Basic Clin Pharm, vol. 7, n. 2, 2016, pp. 27-31, DOI:10.4103/0976-0105.177703, PMC 4804402, PMID 27057123.
Brown, D.C., Resiniferatoxin: The Evolution of the 'Molecular Scalpel' for Chronic Pain Relief, in Pharmaceuticals, vol. 9, n. 3, 2016, p. 47, DOI:10.3390/ph9030047, PMC 5039500, PMID 27529257.

nih.gov

ncbi.nlm.nih.gov

Christopher S. J. Walpole, Similarities and Differences in the Structure-Activity Relationships of Capsaicin and Resiniferatoxin Analogues, in J. Med. Chem., vol. 39, n. 15, 1996, pp. 2939-2952, DOI:10.1021/jm960139d, PMID 8709128.
Szallasi A, Blumberg PM, Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analogue of capsaicin, the irritant constituent in red pepper, in Neuroscience, vol. 30, n. 2, 1989, pp. 515-520, DOI:10.1016/0306-4522(89)90269-8, PMID 2747924.
Szallasi A, Blumberg PM, Resiniferatoxin and its analogues provide novel insights into the pharmacology of the vanilloid (capsaicin) receptor, in Life Sci., vol. 47, n. 16, 1990, pp. 1399-1408, DOI:10.1016/0024-3205(90)90518-V, PMID 2174484.
Szallasi A, Blumberg PM, Vanilloid receptor loss in rat sensory ganglia associated with long term desensitization to resiniferatoxin, in Neurosci. Lett., vol. 140, n. 1, 1992, pp. 51-54, DOI:10.1016/0304-3940(92)90679-2, PMID 1407700.
Olah Z, etal, Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1, in J. Biol. Chem., vol. 276, n. 14, 2001, pp. 11021-11030, DOI:10.1074/jbc.M008392200, PMID 11124944.
Nair AB, Jacob S, A simple practice guide for dose conversion between animals and human, in J Basic Clin Pharm, vol. 7, n. 2, 2016, pp. 27-31, DOI:10.4103/0976-0105.177703, PMC 4804402, PMID 27057123.
Brown, D.C., Resiniferatoxin: The Evolution of the 'Molecular Scalpel' for Chronic Pain Relief, in Pharmaceuticals, vol. 9, n. 3, 2016, p. 47, DOI:10.3390/ph9030047, PMC 5039500, PMID 27529257.

pubchem.ncbi.nlm.nih.gov

Scheda della resiniferatossina su pubchem, su pubchem.ncbi.nlm.nih.gov.

oadoi.org

Christopher S. J. Walpole, Similarities and Differences in the Structure-Activity Relationships of Capsaicin and Resiniferatoxin Analogues, in J. Med. Chem., vol. 39, n. 15, 1996, pp. 2939-2952, DOI:10.1021/jm960139d, PMID 8709128.
Olah Z, etal, Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1, in J. Biol. Chem., vol. 276, n. 14, 2001, pp. 11021-11030, DOI:10.1074/jbc.M008392200, PMID 11124944.

scbt.com

datasheets.scbt.com

Material Safety Data Sheet for resiniferatoxin, 2009 (PDF), su datasheets.scbt.com.

springer.com

adisinsight.springer.com

Resiniferatoxin - Sorrento Therapeutics - AdisInsight, su adisinsight.springer.com, 24 gennaio 2019.

zenodo.org

Szallasi A, Blumberg PM, Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analogue of capsaicin, the irritant constituent in red pepper, in Neuroscience, vol. 30, n. 2, 1989, pp. 515-520, DOI:10.1016/0306-4522(89)90269-8, PMID 2747924.
Szallasi A, Blumberg PM, Resiniferatoxin and its analogues provide novel insights into the pharmacology of the vanilloid (capsaicin) receptor, in Life Sci., vol. 47, n. 16, 1990, pp. 1399-1408, DOI:10.1016/0024-3205(90)90518-V, PMID 2174484.
Szallasi A, Blumberg PM, Vanilloid receptor loss in rat sensory ganglia associated with long term desensitization to resiniferatoxin, in Neurosci. Lett., vol. 140, n. 1, 1992, pp. 51-54, DOI:10.1016/0304-3940(92)90679-2, PMID 1407700.