Results 371 to 380 of about 22,248,138 (428)

Substance P

Journal of Medicinal Chemistry, 1982
B E, Sandberg, L L, Iversen
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Substance P equals pain substance?

Nature, 1998
Circumstantial evidence has led to the theory that substance P (SP) — an undecapeptide discovered over 60 years ago — is involved in the transmission of pain information from the central nervous system. More direct evidence is now provided by two studies of mice in which the function of SP has been genetically disrupted.
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SUBSTANCE P

Life Sciences, 1974
Susan E. Leeman, Edmund A. Mroz
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Upregulated expression of substance P in basophils of the patients with chronic spontaneous urticaria: induction of histamine release and basophil accumulation by substance P

Cell Biology and Toxicology, 2016
Wenjiao Zheng, Junling Wang, Wei Zhu, Chiyan Xu, Shaoheng He   +4 more
semanticscholar   +1 more source

Substance P and Fibromyalgia

Journal of Musculoskeletal Pain, 1998
(1998). Substance P and Fibromyalgia. Journal of Musculoskeletal Pain: Vol. 6, No. 3, pp. 29-35.
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Role of substance P in the cardiovascular system

Neuropeptides, 2016
E. Mistrová, P. Kruzliak, M. Dvoráková   +2 more
semanticscholar   +1 more source

Substance P: A Neuropeptide

American Journal of Psychiatry, 2006
Eugenia Kuteeva, Tomas Hokfelt
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Studies of Substance P

1966
The physiological role of substance P (SP) is still largely a matter of conjecture. Its extremely high potency in pharmacological tests (stimulation of gut, depression of blood pressure, and vasodilation), its almost exclusive occurrence in the gut and certain areas of the brain (Pernow 1953; Lembeck and Zetler, 1962; McLennan, 1963), and its ...
Lyman C. Craig, Harry Meinardi
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Involvement of substance P and the NK-1 receptor in human pathology

Amino Acids, 2014
M. Muñoz, R. Coveñas
semanticscholar   +1 more source

Are the proposed substance P receptor sub-types, substance P receptors?

Life Sciences, 1984
Recently, a number of laboratories have postulated the existence of receptor sub-types for substance P. This review is intended to represent a critical appraisal of these reports. In the majority of cases, the evidence for the existence of receptor sub-types has been obtained from observed potency differences of agonists.
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