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Massive Prosthetic Valve Thrombus in a Patient With Idiopathic Hypereosinophilic Syndrome

Journal of cardiothoracic and vascular anesthesia, 2007-06, Vol.21 (3), p.434-435

2007

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Activation of three types of voltage‐independent Ca2+ channel in A7r5 cells by endothelin‐1 as revealed by a novel Ca2+ channel blocker LOE 908

British journal of pharmacology, 1999-03, Vol.126 (5), p.1107-1114

1999

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Pharmacological characterization of Ca2+ entry channels in endothelin‐1‐induced contraction of rat aorta using LOE 908 and SK&F 96365

British journal of pharmacology, 1999-07, Vol.127 (6), p.1388-1398

1999

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Activation of two types of Ca2+‐permeable nonselective cation channel by endothelin‐1 in A7r5 cells

British journal of pharmacology, 1998-08, Vol.124 (7), p.1541-1549

1998

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Inhibitory effect of nitrovasodilators and cyclic GMP on ET‐1‐activated Ca2+‐permeable nonselective cation channel in rat aortic smooth muscle cells

British journal of pharmacology, 1997-04, Vol.120 (8), p.1536-1544

1997

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Long‐lasting activation of cation current by low concentration of endothelin‐1 in mouse fibroblasts and smooth muscle cells of rabbit aorta

British journal of pharmacology, 1995-06, Vol.115 (3), p.479-485

1995

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Comparative contractile effects of Halothane and sevoflurane in rat aorta

Anesthesiology (Philadelphia), 2000, Vol.92 (1), p.219-227

2000

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The involvement of a novel mechanism distinct from the thrombin receptor in the vasocontraction induced by trypsin

British journal of pharmacology, 1997-03, Vol.120 (5), p.851-856

1997

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Physiological Role of Ca2+-Permeable Nonselective Cation Channel in Endothelin-1-Induced Contraction of Rabbit Aorta

Journal of cardiovascular pharmacology, 1997-10, Vol.30 (4), p.504-509

1997

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Activation of two types of Ca 2+ ‐permeable nonselective cation channel by endothelin‐1 in A7r5 cells

British journal of pharmacology, 2009-02, Vol.124 (7), p.1541-1549

2009

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Inhibitory effect of nitrovasodilators and cyclic GMP on ET‐1‐activated Ca 2+ ‐permeable nonselective cation channel in rat aortic smooth muscle cells

British journal of pharmacology, 2009-02, Vol.120 (8), p.1536-1544

2009

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Activation of three types of voltage‐independent Ca 2+ channel in A7r5 cells by endothelin‐1 as revealed by a novel Ca 2+ channel blocker LOE 908

British journal of pharmacology, 2009-01, Vol.126 (5), p.1107-1114

2009

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Pharmacological characterization of Ca 2+ entry channels in endothelin‐1‐induced contraction of rat aorta using LOE 908 and SK&F 96365

British journal of pharmacology, 2009-01, Vol.127 (6), p.1388-1398

2009

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Ca(2+) channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

American Journal of Physiology: Cell Physiology, 2001-11, Vol.281 (5), p.C1676-C1685

2001

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Ca2+ channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

American Journal of Physiology: Cell Physiology, 2001-11, Vol.281 (5), p.C1676

2001

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Distinct subdomains of human endothelin receptors determine their selectivity to endothelinA-selective antagonist and endothelinB-selective agonists

The Journal of biological chemistry, 1993-04, Vol.268 (12), p.8547-8553

1993

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Thiopental Induces Contraction of Rat Aortic Smooth Muscle Through Ca2+ Release from the Sarcoplasmic Reticulum

Anesthesia and analgesia, 2000-07, Vol.91 (1), p.62-67

2000

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Ca super(2+) channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

American Journal of Physiology: Cell Physiology, 2001-11, Vol.281 (5), p.C1676-C1685

2001

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Ca 2+ channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

American Journal of Physiology: Cell Physiology, 2001-11, Vol.281 (5), p.C1676-C1685

2001

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Inhibitory effect of nitrovasodilators and cyclic GMP on ET-1-activated Ca(2+)-permeable nonselective cation channel in rat aortic smooth muscle cells

British journal of pharmacology, 1997-04, Vol.120 (8), p.1536-1544

1997

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Thiopental induces contraction of rat aortic smooth muscle through Ca(2+) release from the sarcoplasmic reticulum

Anesthesia and analgesia, 2000-07, Vol.91 (1), p.62-67

2000

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Thiopental induces contraction of rat aortic smooth muscle through Ca2+ release from the sarcoplasmic reticulum

Anesthesia and analgesia, 2000-07, Vol.91 (1), p.62-67

2000

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Ca2+ Entry Channels in Rat Thoracic Aortic Smooth Muscle Cells Activated by Endothelin-1

The Japanese Journal of Pharmacology, 1999, Vol.80(4), pp.281-288

1999

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Ca2+ channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

American Journal of Physiology: Cell Physiology, 2001-11, Vol.50 (5), p.C1676-C1685

2001

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Functional coupling of ETA rceptor with Ca2+ -permeable nonselective cation channel

Folia Pharmacologica Japonica, 1996, Vol.108(supplement), pp.93-98

1996

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Massive Prosthetic Valve Thrombus in a Patient With Idiopathic Hypereosinophilic Syndrome

Activation of three types of voltage‐independent Ca2+ channel in A7r5 cells by endothelin‐1 as revealed by a novel Ca2+ channel blocker LOE 908

Pharmacological characterization of Ca2+ entry channels in endothelin‐1‐induced contraction of rat aorta using LOE 908 and SK&F 96365

Activation of two types of Ca2+‐permeable nonselective cation channel by endothelin‐1 in A7r5 cells

Inhibitory effect of nitrovasodilators and cyclic GMP on ET‐1‐activated Ca2+‐permeable nonselective cation channel in rat aortic smooth muscle cells

Long‐lasting activation of cation current by low concentration of endothelin‐1 in mouse fibroblasts and smooth muscle cells of rabbit aorta

Comparative contractile effects of Halothane and sevoflurane in rat aorta

The involvement of a novel mechanism distinct from the thrombin receptor in the vasocontraction induced by trypsin

Physiological Role of Ca2+-Permeable Nonselective Cation Channel in Endothelin-1-Induced Contraction of Rabbit Aorta

Activation of two types of Ca 2+ ‐permeable nonselective cation channel by endothelin‐1 in A7r5 cells

Inhibitory effect of nitrovasodilators and cyclic GMP on ET‐1‐activated Ca 2+ ‐permeable nonselective cation channel in rat aortic smooth muscle cells

Activation of three types of voltage‐independent Ca 2+ channel in A7r5 cells by endothelin‐1 as revealed by a novel Ca 2+ channel blocker LOE 908

Pharmacological characterization of Ca 2+ entry channels in endothelin‐1‐induced contraction of rat aorta using LOE 908 and SK&F 96365

Ca(2+) channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

Ca2+ channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

Distinct subdomains of human endothelin receptors determine their selectivity to endothelinA-selective antagonist and endothelinB-selective agonists

Thiopental Induces Contraction of Rat Aortic Smooth Muscle Through Ca2+ Release from the Sarcoplasmic Reticulum

Ca super(2+) channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

Ca 2+ channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

Inhibitory effect of nitrovasodilators and cyclic GMP on ET-1-activated Ca(2+)-permeable nonselective cation channel in rat aortic smooth muscle cells

Thiopental induces contraction of rat aortic smooth muscle through Ca(2+) release from the sarcoplasmic reticulum

Thiopental induces contraction of rat aortic smooth muscle through Ca2+ release from the sarcoplasmic reticulum

Ca2+ Entry Channels in Rat Thoracic Aortic Smooth Muscle Cells Activated by Endothelin-1

Ca2+ channels activated by endothelin-1 in CHO cells expressing endothelin-A or endothelin-B receptors

Functional coupling of ETA rceptor with Ca2+ -permeable nonselective cation channel

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