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Leukemia Inhibitory Factor Influences the Fate Choice of Mesenchymal Progenitor Cells

Stem cells (Dayton, Ohio), 2007-02, Vol.25 (2), p.305-312

2007

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The PPARgamma-selective ligand BRL-49653 differentially regulates the fate choices of rat calvaria versus rat bone marrow stromal cell populations

BMC developmental biology, 2008-07, Vol.8 (1), p.71-71, Article 71

2008

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Discovery and structure–activity relationship of thienopyridine derivatives as bone anabolic agents

Bioorganic & medicinal chemistry, 2013-04, Vol.21 (7), p.1628-1642

2013

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A subset of osteoblasts expressing high endogenous levels of PPARgamma switches fate to adipocytes in the rat calvaria cell culture model

PloS one, 2010-07, Vol.5 (7), p.e11782-e11782

2010

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A Subset of Osteoblasts Expressing High Endogenous Levels of PPARγ Switches Fate to Adipocytes in the Rat Calvaria Cell Culture Model

PloS one, 2010-07, Vol.5 (7), p.e11782

2010

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A Subset of Osteoblasts Expressing High Endogenous Levels of PPAR[gamma] Switches Fate to Adipocytes in the Rat Calvaria Cell Culture Model

PloS one, 2010-07, Vol.5 (7), p.e11782

2010

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A Novel Bone Resorption Inhibitor, A-75943 Isolated from Streptomyces sp. SANK 61296

The Journal of Antibiotics, 1998/06/25, Vol.51(6), pp.531-538

1998

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Effects of Dihydropyridine Ca Blockers on the Renal Function in Nephrotic Spontaneously Hypertensive Rat (SHR)

Biological and Pharmaceutical Bulletin, 1994/03/15, Vol.17(3), pp.407-410

1994

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Novel 2-Amino-1, 4-dihydropyridine Calcium Antagonists. I. Synthesis and Antihypertensive Effects of 2-Amino-1, 4-dihydropyridine Derivatives Having Nitroxyalkoxycarbonyl Groups at 3- and/or 5-Position

Chemical and Pharmaceutical Bulletin, 1995/05/15, Vol.43(5), pp.788-796

1995

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A Subset of Osteoblasts Expressing High Endogenous Levels of PPARg Switches Fate to Adipocytes in the Rat Calvaria Cell Culture Model

PloS one, 2010-07, Vol.5 (7)

2010

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Novel 2-Amino-1, 4-dihydropyridine Calcium Antagonists. II. Synthesis and Antihypertensive Effects of 2-Amino-1, 4-dihydropyridine Derivatives Having N, N-Dialkylaminoalkoxycarbonyl Groups at 3- and/or 5-Position

Chemical and Pharmaceutical Bulletin, 1995/05/15, Vol.43(5), pp.797-817

1995

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Angiotensin-converting enzyme inhibitors. Perhydro-1,4-thiazepin-5-one derivatives

Journal of medicinal chemistry, 1987-11, Vol.30 (11), p.1984-1991

1987

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Antihypertensive Effect of CS-905, a Novel Dihydropyridine Calcium Blocker, in Conscious Hypertensive Dogs

The Japanese Journal of Pharmacology, 1990, Vol.53(2), pp.264-266

1990

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Studies of Novel 1, 4-Dihydropyridine Ca Antagonist CS-905. I. Measurement of Partition Coefficient (logP) by High Performance Liquid Chromatography (HPLC)

Yakugaku zasshi, 1995, Vol.115 (3), p.213-220

1995

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Effects of CS-905, a novel dihydropyridine calcium channel blocker, on arterial pressure, renal excretory function, and inner medullary blood flow in the rat

American journal of hypertension, 1994-07, Vol.7 (7), p.637-646

1994

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Pharmacological Profiles of CS-622, a Novel Angiotensin Converting Enzyme Inhibitor

The Japanese Journal of Pharmacology, 1988, Vol.48(3), pp.349-356

1988

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Hemodynamic Changes Following Long-Term Administration of CS-905, a Novel Dihydropyridine Calcium Blocker, in Conscious SHR

The Japanese Journal of Pharmacology, 1990, Vol.54(1), pp.1-6

1990

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Effects of RS-1893, a Novel Cardiotonic Agent on Central and Peripheral Hemodynamics in Anesthetized Rats

Japanese Journal of Pharmacology, 1989, Vol.51 (4), p.577-580

1989

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Antihypertensive Effects of CS-905, a Novel Dihydropyridine Ca++ Channel Blocker

The Japanese Journal of Pharmacology, 1989, Vol.51(1), pp.57-64

1989

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Antihypertensive effects of CS-866, a novel angiotensin II receptor (AT1) antagonist, in rats

Japanese Journal of Pharmacology, 1996, Vol.71 (suppl.2), p.326-326

1996

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Effects of long-term administration of CS-622, a novel ACE inhibitor, on abnormal Ca++ permeability of SHR aorta

Japanese Journal of Pharmacology, 1988, Vol.46 (suppl), p.95-95

1988

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Beneficial Renal Effects of CS-905, a Novel Dihydropyridine Calcium Blocker, in SHR

Japanese Journal of Pharmacology, 1989-01, Vol.51 (4), p.501-508

1989

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Antihypertensive Effects of CS-905, a Novel Dihydropyridine Ca++ Channel Blocker

Japanese Journal of Pharmacology, 1989, Vol.51 (1), p.57-64

1989

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Beneficial Renal Effects of CS-905, a Novel Dihydropyridine Calcium Blocker, in SHR

The Japanese Journal of Pharmacology, 1989, Vol.51(4), pp.501-508

1989

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Antiatherogenic effect of CS-905, a new calcium antagonist in cholesterol-fed rabbits

Japanese Journal of Pharmacology, 1992, Vol.58 (suppl.2), p.342-342

1992

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Leukemia Inhibitory Factor Influences the Fate Choice of Mesenchymal Progenitor Cells

The PPARgamma-selective ligand BRL-49653 differentially regulates the fate choices of rat calvaria versus rat bone marrow stromal cell populations

Discovery and structure–activity relationship of thienopyridine derivatives as bone anabolic agents

A subset of osteoblasts expressing high endogenous levels of PPARgamma switches fate to adipocytes in the rat calvaria cell culture model

A Subset of Osteoblasts Expressing High Endogenous Levels of PPARγ Switches Fate to Adipocytes in the Rat Calvaria Cell Culture Model

A Subset of Osteoblasts Expressing High Endogenous Levels of PPAR[gamma] Switches Fate to Adipocytes in the Rat Calvaria Cell Culture Model

A Novel Bone Resorption Inhibitor, A-75943 Isolated from Streptomyces sp. SANK 61296

Effects of Dihydropyridine Ca Blockers on the Renal Function in Nephrotic Spontaneously Hypertensive Rat (SHR)

Novel 2-Amino-1, 4-dihydropyridine Calcium Antagonists. I. Synthesis and Antihypertensive Effects of 2-Amino-1, 4-dihydropyridine Derivatives Having Nitroxyalkoxycarbonyl Groups at 3- and/or 5-Position

A Subset of Osteoblasts Expressing High Endogenous Levels of PPARg Switches Fate to Adipocytes in the Rat Calvaria Cell Culture Model

Novel 2-Amino-1, 4-dihydropyridine Calcium Antagonists. II. Synthesis and Antihypertensive Effects of 2-Amino-1, 4-dihydropyridine Derivatives Having N, N-Dialkylaminoalkoxycarbonyl Groups at 3- and/or 5-Position

Angiotensin-converting enzyme inhibitors. Perhydro-1,4-thiazepin-5-one derivatives

Antihypertensive Effect of CS-905, a Novel Dihydropyridine Calcium Blocker, in Conscious Hypertensive Dogs

Studies of Novel 1, 4-Dihydropyridine Ca Antagonist CS-905. I. Measurement of Partition Coefficient (logP) by High Performance Liquid Chromatography (HPLC)

Effects of CS-905, a novel dihydropyridine calcium channel blocker, on arterial pressure, renal excretory function, and inner medullary blood flow in the rat

Pharmacological Profiles of CS-622, a Novel Angiotensin Converting Enzyme Inhibitor

Hemodynamic Changes Following Long-Term Administration of CS-905, a Novel Dihydropyridine Calcium Blocker, in Conscious SHR

Effects of RS-1893, a Novel Cardiotonic Agent on Central and Peripheral Hemodynamics in Anesthetized Rats

Antihypertensive Effects of CS-905, a Novel Dihydropyridine Ca++ Channel Blocker

Antihypertensive effects of CS-866, a novel angiotensin II receptor (AT1) antagonist, in rats

Effects of long-term administration of CS-622, a novel ACE inhibitor, on abnormal Ca++ permeability of SHR aorta

Beneficial Renal Effects of CS-905, a Novel Dihydropyridine Calcium Blocker, in SHR

Antihypertensive Effects of CS-905, a Novel Dihydropyridine Ca++ Channel Blocker

Beneficial Renal Effects of CS-905, a Novel Dihydropyridine Calcium Blocker, in SHR

Antiatherogenic effect of CS-905, a new calcium antagonist in cholesterol-fed rabbits

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