scholarly journals Non-selective cationic channels of smooth muscle and the mammalian homologues ofDrosophilaTRP

2004 ◽  
Vol 559 (3) ◽  
pp. 685-706 ◽  
Author(s):  
D. J. Beech ◽  
K. Muraki ◽  
R. Flemming
Keyword(s):  
Smooth Muscle ◽  
Cationic Channels

Muscarinic receptors activating cationic channels in smooth muscle

Life Sciences ◽  
1997 ◽  
Vol 60 (13-14) ◽  
pp. 1186
Author(s):  
Alexander V. Zholos ◽  
Thomas B. Bolton
Keyword(s):  
Smooth Muscle ◽  
Muscarinic Receptors ◽  
Cationic Channels

TRPC and SOC Cationic Channels in Vascular Smooth Muscle

2003 ◽  
Vol 35 (3/4) ◽  
pp. 154
Author(s):  
D. J. Beech ◽  
S. Z. Xu ◽  
R. Flemming ◽  
D. McHugh ◽  
F. Zeng
Keyword(s):  
Smooth Muscle ◽  
Vascular Smooth Muscle ◽  
Cationic Channels

Hyperpolarization-activated cationic channels in smooth muscle cells are stretch sensitive

1991 ◽  
Vol 417 (5) ◽  
pp. 493-499 ◽  
Author(s):  
Tetsuya Hisada ◽  
Richard W. Ordway ◽  
Michael T. Kirber ◽  
Joshua J. Singer ◽  
John V. Walsh
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Muscle Cells ◽  
Cationic Channels

Stretch-inactivated cationic channels in single smooth muscle cells

1993 ◽  
Vol 422 (4) ◽  
pp. 393-396 ◽  
Author(s):  
Tetsuya Hisada ◽  
John V. Walsh ◽  
Joshua J. Singer
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Muscle Cells ◽  
Cationic Channels

Non-selective cationic channels (NSCC) in smooth muscle cells from human umbilical arteries

Placenta ◽  
2004 ◽  
Vol 25 (8-9) ◽  
pp. 723-729 ◽  
Author(s):  
J. Raingo ◽  
A. Rebolledo ◽  
F. Iveli ◽  
A.O. Grassi de Gende ◽  
V. Milesi
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Muscle Cells ◽  
Cationic Channels ◽  
Umbilical Arteries

The Cellular Origin in Atheromatous Lesion

1970 ◽  
Vol 28 ◽  
pp. 202-203
Author(s):  
T. M. Murad ◽  
H. A. I. Newman ◽  
K. F. Kern
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Rabbit Aorta ◽  
Mixed Population ◽  
The Other ◽  
Cellular Origin ◽  
Ultrastructural Studies ◽  
Atherosclerotic Lesions ◽  
Show Evidence ◽  
Early Lesion

The origin of lipid containing cells in atheromatous lesion has been disputed. Geer in his study on atheromatous lesions of rabbit aorta, suggested that the early lesion is composed mainly of lipid-laden macrophages and the later lesion has a mixed population of macrophages and smooth muscle cells. Parker on the other hand, was able to show evidence that the rabbit lesion is primarily composed of lipid-laden cells of smooth muscle origin. The above studies and many others were done on an intact lesion without any attempt of cellular isolation previous to their ultrastructural studies. Cell isolation procedures have been established for atherosclerotic lesions through collagenase and elastase digestion Therefore this procedure can be utilized to identify the cells involved in rabbit atheroma.

Electron Probe Analysis of Muscle

1982 ◽  
Vol 40 ◽  
pp. 398-401
Author(s):  
A. V. Somlyo ◽  
H. Shuman ◽  
A. P. Somlyo
Keyword(s):  
Skeletal Muscle ◽  
Smooth Muscle ◽  
Sarcoplasmic Reticulum ◽  
Resting State ◽  
Binding Sites ◽  
Electron Probe ◽  
Frog Skeletal Muscle ◽  
Electron Probe Analysis ◽  
Probe Analysis

Electron probe analysis of frozen dried cryosections of frog skeletal muscle, rabbit vascular smooth muscle and of isolated, hyperpermeab1 e rabbit cardiac myocytes has been used to determine the composition of the cytoplasm and organelles in the resting state as well as during contraction. The concentration of elements within the organelles reflects the permeabilities of the organelle membranes to the cytoplasmic ions as well as binding sites. The measurements of [Ca] in the sarcoplasmic reticulum (SR) and mitochondria at rest and during contraction, have direct bearing on their role as release and/or storage sites for Ca in situ.

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