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Mouse Vas Deferens

Known as: Vas Deferens (MMHCC) 
National Institutes of Health

Papers overview

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Highly Cited
1998
Highly Cited
1998
Isolation and partial characterization of an opioid-like 88 kDa hibernation-related protein.
Highly Cited
1992
Highly Cited
1992
Conformationally restrained analogues of pravadoline: nanomolar potent, enantioselective, (aminoalkyl)indole agonists of the cannabinoid receptor.
Pravadoline (1) is an (aminoalkyl)indole analgesic agent which is an inhibitor of cyclooxygenase and, in contrast to other NSAIDs… 
Highly Cited
1990
Highly Cited
1990
Design of peptidomimetic delta opioid receptor antagonists using the message-address concept.
Highly selective nonpeptide ligands with potent delta opioid receptor antagonist activity have been developed using the message… 
1986
1986
Opiate receptor binding affinities of some D-amino acid substituted β-casomorphin analogs
1985
1985
TENA, a selective kappa opioid receptor antagonist.
Highly Cited
1983
Highly Cited
1983
Cyclic penicillamine containing enkephalin analogs display profound delta receptor selectivities.
Highly Cited
1983
Highly Cited
1983
Conformationally constrained cyclic enkephalin analogs with pronounced delta opioid receptor agonist selectivity.
Highly Cited
1981
Highly Cited
1981
Opioid activities of beta-casomorphins.
Highly Cited
1981
Highly Cited
1981
Synthetic peptides related to the dermorphins. I. Synthesis and biological activities of the shorter homologues and of analogues of the heptapeptides
Highly Cited
1980
Highly Cited
1980
Selective development of tolerance without dependence in multiple opiate receptors of mouse vas deferens
Studies with isolated tissues have provided strong indications for a multiplicity of opiate receptors 1–4. To satisfy the… 
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