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Disease Info Card
Morphine Dependence
Information about Morphine Dependence: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Morphine Dependence
Most recent studies have shown that Morphine Dependence shares some biological mechanisms with blepharoptosis, depressive-disorder, diarrhea, nervousness, opioid-withdrawal, pain, patient-dependence-on, physical-dependence, stereotyped-behavior, substance-related-disorders, substance-withdrawal-syndrome, teeth-chattering, tremor-unspecified, withdrawal-sign-or-symptom.
Among the many pathways, these few ones have gauged particular interests from scientists studying Morphine Dependence, and have been seen in publications frequently: Circadian Rhythm, Conditioned Taste Aversion, Corticosterone Secretion, Defecation, Endocytosis, Excretion, Habituation, Hypersensitivity, Immune Response, Localization, Locomotion, Mastication, Oxytocin Secretion, Pathogenesis, Reflex, Response To Morphine, Secretion, Sensitization, Synaptic Transmission, Transport
Quite a number of genes have been found to play important roles in Morphine Dependence, such as AVP, CCK, CPA1, CREB1, CRH, EPHB2, ERMAP, FOS, MAPK1, MME, NOS1, NOS2, OPRM1, PNOC, POMC, PRRT2, TAC1, TH. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.