Zobrazeno 1 - 10
of 496
pro vyhledávání: '"Wollemann"'
Autor:
Maria Wollemann, Catherine Rougeot
Publikováno v:
Current Bioactive Compounds. 12:230-235
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::135f0ff63a3ae437bdbde3a14b96e8e8
https://doi.org/10.2174/1573407212666160425171005
https://doi.org/10.2174/1573407212666160425171005
Publikováno v:
In Hormones and Behavior 2003 43(2):302-311
Publikováno v:
Brain Research Bulletin. 90:114-117
The purpose of the present study was to elucidate the role of protein kinase A and C in the mechanism of capsaicin inhibition on mu-opiate receptors. H89, a protein kinase A inhibitor and BIM (bisindolylmaleimide), a protein kinase C inhibitor were u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3ea567081dcde42330d57d23830cbc0
https://doi.org/10.1016/j.brainresbull.2012.10.008
https://doi.org/10.1016/j.brainresbull.2012.10.008
Autor:
Röpstorff, Riebeck, Virchow, Zapf, Handtmann, Forrer, Voss, Wollemann, Undset, Henning, Schwartz, W., Bartels, Jacobsen, Hartwich, Fritsch, v. Schulenburg, Oppert, H.
Publikováno v:
Zeitschrift für Ethnologie, 1883 Jan 01. 15, 509-538.
Externí odkaz:
https://www.jstor.org/stable/23026615
Publikováno v:
Regulatory Peptides. 178:71-75
Endogenously occurring opioid peptides are rapidly metabolized by different ectopeptidases. Human opiorphin is a recently discovered natural inhibitor of the enkephalin-inactivating neutral endopeptidase (NEP) and aminopeptidase-N (AP-N) (Wisner et a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d701cc0057e4718b067ac70adfaa5c2
https://doi.org/10.1016/j.regpep.2012.06.011
https://doi.org/10.1016/j.regpep.2012.06.011
Autor:
Maria Wollemann, Krisztina Csabafi, Gyula Telegdy, Zsolt Bagosi, Miklós Jászberényi, Géza Tóth
Publikováno v:
Peptides. 32:1656-1660
The neuroendocrine and behavioral effects of Tyr- d -Ala-Gly-Phe- d -Nle-Arg-Phe (DADN), a more stable derivative of the endogenous opiate Met-enkephalin related peptide Met 5 -enkephalin-Arg 6 -Phe 7 were investigated in mice. The behavioral experim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51d4d5b5f9f5ce33c237e4fe811520dd
https://doi.org/10.1016/j.peptides.2011.05.029
https://doi.org/10.1016/j.peptides.2011.05.029
Publikováno v:
Brain Research Bulletin. 77:136-142
Capsaicin inhibited the equilibrium specific binding of endogenous opioid-like peptide ligands such as endomorphin-1, nociceptin, and dynorphin (1–17) in rat brain membrane preparations. We studied the in vitro effect of capsaicin (1–10 μM) on h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee6a34a74b7805b1937242537e83bac4
https://doi.org/10.1016/j.brainresbull.2008.06.003
https://doi.org/10.1016/j.brainresbull.2008.06.003
Autor:
Ferenc Zádor, Maria Wollemann
Publikováno v:
Pharmacological research. 102
A growing amount of data demonstrates the interactions between cannabinoid, opioid and the transient receptor potential (TRP) vanilloid type 1 (TRPV1) receptors. These interactions can be bidirectional, inhibitory or excitatory, acute or chronic in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b4b53a93fda29312eb6b606b91a892
https://pubmed.ncbi.nlm.nih.gov/26520391
https://pubmed.ncbi.nlm.nih.gov/26520391
Publikováno v:
Archives of medical research. 46(6)
Opioid peptides are potent analgesics with therapeutic potential in the treatment of acute and chronic pain. Their efficacy is limited by peptidases (enkephalinases). Opiorphin pentapeptide (QRFSR) is the first characterized human endogenous inhibito
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::383eac6c393affe0885eabc7c4ffd099
https://pubmed.ncbi.nlm.nih.gov/26143971
https://pubmed.ncbi.nlm.nih.gov/26143971
Autor:
Maria Wollemann
Publikováno v:
Acta Biologica Hungarica. 54:139-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42e2ff6b34fd50adda9115a3b8d760ba
https://doi.org/10.1556/abiol.54.2003.2.2
https://doi.org/10.1556/abiol.54.2003.2.2