Dr. Laine J Murphey MD
Internist
1435 G St Springfield OR, 97477About
Dr. Laine Murphey is an internist practicing in Nashville, TN. Dr. Murphey specializes in the medical treatment of adults. Internists can act as a primary physician or a consultant to a primary physician. They manage both common and rare diseases. Dr. Murphey provides comprehensive care and manages treatment with surgeons as well. Internists establish long-term relationships with their patients and incorporate disease prevention and mental health care into their practice.
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Angiotensin-converting enzyme insertion/deletion polymorphism modulates the human in vivo metabolism of bradykinin.
- Endogenous bradykinin and the renin and pressor responses to furosemide in humans.
- Bradykinin stimulates tissue plasminogen activator release from human forearm vasculature through B(2) receptor-dependent, NO synthase-independent, and cyclooxygenase-independent pathway.
- Angiotensin-(1-7) does not affect vasodilator or TPA responses to bradykinin in human forearm.
- Interactive effect of PAI-1 4G/5G genotype and salt intake on PAI-1 antigen.
- Dipeptidyl peptidase IV activity in patients with ACE-inhibitor-associated angioedema.
- Ethnicity affects vasodilation, but not endothelial tissue plasminogen activator release, in response to bradykinin.
- Effect of combined AT1 receptor and aldosterone receptor antagonism on plasminogen activator inhibitor-1.
- Angiotensin-converting enzyme inhibition and smoking potentiate the kinin response to cardiopulmonary bypass.
- Angiotensin-converting enzyme inhibition increases basal vascular tissue plasminogen activator release in women but not in men.
- A pilot study indicating that bradykinin B2 receptor antagonism attenuates protamine-related hypotension after cardiopulmonary bypass.
- Bradykinin B(2) receptor does not contribute to blood pressure lowering during AT(1) receptor blockade.
- Pharmacokinetics and metabolism of cocaine in maternal and fetal guinea pigs.
- Developmental change of mu opioid receptors in neonatal guinea pig brain stem.
- Cocaine metabolites in the neonate: potential for toxicity.
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