Peptides in the cat carotid body (glomus caroticum): VIP-, enkephalin-, and substance P-like immunoreactivity

Acta Physiologica Scandinavica
J J LundbergL Terenius

Abstract

No abstract listed.

References

Dec 1, 1978·Journal of Neurochemistry·J Fahrenkrug, O B Schaffalitzky de Muckadell
Apr 1, 1977·Brain Research·J FahrenkrugA Fahrenkrug
May 1, 1969·The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society·A G Pearse
May 22, 1973·Histochemie. Histochemistry. Histochimie·G GöthlinH Helminen
May 18, 1956·Acta Physiologica Scandinavica·U S VON EULER, B PERNOW

Citations

Oct 18, 2002·Microscopy Research and Technique·Tatsumi Kusakabe
Nov 1, 1980·Naunyn-Schmiedeberg's Archives of Pharmacology·G Haeusler, R Osterwalder
Feb 1, 1991·Respiration Physiology·M Pokorski, S Lahiri
Mar 1, 1994·Respiration Physiology·P A CraggN R Prabhakar
Jan 1, 1983·Journal of the Autonomic Nervous System·O H Viveros, S P Wilson
Dec 1, 1987·Journal of the Autonomic Nervous System·D S KnightT S Fournet
Aug 1, 1991·Journal of the Autonomic Nervous System·M ShirahataS Lahiri
Jan 1, 1980·Peptides·G A OlsonD H Coy
Jan 1, 1984·Neurobiology of Aging·M PartanenS I Rapoport
Dec 1, 1980·Neuroscience Letters·M ReineckeW G Forssmann
Mar 1, 1979·Acta Physiologica Scandinavica·B NewsonL M Nyhus
Jul 1, 1984·Acta Physiologica Scandinavica·N R PrabhakarC von Euler
Jul 1, 1993·Archives of Disease in Childhood·L CattarossiF Macagno
Jun 1, 1996·Anesthesia and Analgesia·N WyonS G Lindahl
Jan 1, 1980·Journal of Neural Transmission·R EdinJ Kewenter
Jan 1, 1996·Advances in Neuroimmunology·D L BellingerD L Felten

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