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ZSTK474, a specific phosphatidylinositol 3-kinase inhibitor, induces G1 arrest of the cell cycle in vivo

European journal of cancer (1990), 2012-04, Vol.48 (6), p.936-943

2012

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Sequential Formation of Low-Mass Stars in the BRC 14 Region

Publications of the Astronomical Society of Japan, 2006-08, Vol.58 (4), p.L29-L34

2006

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Identification of candidate predictive markers of anticancer drug sensitivity using a panel of human cancer cell lines

Cancer science, 2003-12, Vol.94 (12), p.1074-1082

2003

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Correlating Phosphatidylinositol 3-Kinase Inhibitor Efficacy with Signaling Pathway Status: In silico and Biological Evaluations

Cancer research (Chicago, Ill.), 2010-06, Vol.70 (12), p.4982-4994

2010

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Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G0/G1 arrest

Biochemical and biophysical research communications, 2009-01, Vol.379 (1), p.104-109

2009

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Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G{sub 0}/G{sub 1} arrest

Biochemical and biophysical research communications, 2009-01, Vol.379 (1)

2009

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Changes in Molecular Structure upon Triplet Excitation of All-trans-Spheroidene in n-Hexane Solution and 15-cis-Spheroidene Bound to the Photo-Reaction Center from Rhodobacter sphaeroides As Revealed by Resonance-Raman Spectroscopy and Normal-Coordinate Analysis

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2002-04, Vol.106 (14), p.3566-3579

2002

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Abstract 4399: In vitro and in vivo evaluations of correlation between the activation status of signaling pathways and the efficacy of anticancer compounds in a panel of JFCR39 human cancer cell lines

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.4399-4399

2011

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Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G 0/G 1 arrest

Biochemical and biophysical research communications, 2009, Vol.379 (1), p.104-109

2009

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Abstract 2655: Visualization of G1 arrest of cell cycle induced by inhibition of PI-3 kinase in cancer cells: in vitro evaluations

Cancer research (Chicago, Ill.), 2011-04, Vol.71 (8_Supplement), p.2655-2655

2011

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Abstract C55: Efficacy of PI3K inhibitors to cancer cells with PIK3CA mutation or loss of PTEN expression

Molecular cancer therapeutics, 2009-12, Vol.8 (12_Supplement), p.C55-C55

2009

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Vibronic Coupling through the In-Phase, CC Stretching Mode Plays a Major Role in the 2Ag - to 1Ag - Internal Conversion of all-trans-β-Carotene

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2000-05, Vol.104 (18), p.4155-4166

2000

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Abstract 2493: Inhibition of phosphoinositide 3-kinase suppressed growth of cancer cells with PIK3CA mutations or loss of PTEN expression via G0/G1 arrest of cell cycle but not apoptosis

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.2493-2493

2010

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Picosecond time-resolved absorption study of all-trans- and 9-cis-retinal: configurational relaxation in the triplet state

Chemical physics letters, 1987-02, Vol.134 (2), p.166-170

1987

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Dependence of the triplet potential of retinal homologs on the chain length: resonance Raman spectroscopy and analysis of triplet-sensitized isomerization

Journal of physical chemistry (1952), 1990-05, Vol.94 (10), p.4042-4051

1990

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EFFECT OF PROTONATION ON THE ISOMERIZATION PROPERTIES OF n-BUTYLAMINE SCHIFF BASE OF ISOMERIC RETINAL AS REVEALED BY DIRECT HPLC ANALYSES: SELECTION OF ISOMERIZATION PATHWAYS BY RETINAL PROTEINS

Photochemistry and photobiology, 1991-09, Vol.54 (3), p.433-443

1991

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Transient Raman spectra of the all-trans and 7-, 9-, 11- and 13-mono-cis isomers of retinal and the mechanism of the cis-trans isomerization in the lowest excited triplet state

Chemical physics letters, 1984-06, Vol.107 (4), p.355-359

1984

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Vibronic Coupling through the In-Phase, CC Stretching Mode Plays a Major Role in the 2A g - to 1A g - Internal Conversion of all - trans -β-Carotene

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2000-05, Vol.104 (18), p.4155-4166

2000

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COMPARISON OF THE PATHWAYS AND QUANTUM YIELDS OF DIRECT PHOTOISOMERIZATION OF UNPROTONATED AND PROTONATED N-BUTYLAMINE SCHIFF BASES OF ISOMERIC RETINYLIDENEACETALDEHYDE WITH THOSE OF SCHIFF BASES OF ISOMERIC RETINAL: RATIONALIZATION OF THE SELECTION OF THE RETINYLIDENE CHROMOPHORE BY RETINOCHROME

Photochemistry and photobiology, 1992-12, Vol.56 (6), p.965-975

1992

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ISOMERIZATION OF THE RETINYLIDENE CHROMOPHORE OF BACTERIORHODOPSIN IN LIGHT ADAPTATION: INTRINSIC ISOMERIZATION OF THE CHROMOPHORE AND ITS CONTROL BY THE APO-PROTEIN

Photochemistry and photobiology, 1993-04, Vol.57 (4), p.732-738

1993

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Changes in Molecular Structure upon Triplet Excitation of All-trans-Spheroidene in n-Hexane Solution and 15-cis-Spheroidene Bound to the Photo-Reaction Center from Rhodobacter s phaeroides As Revealed by Resonance-Raman Spectroscopy and Normal-Coordinate Analysis

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2002-04, Vol.106 (14), p.3566-3579

2002

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Transient raman spectra of all-trans, 7-cis, 9-cis, 11-cis and 13-cis retinylideneacetaldehyde. Structures of triplet species as revealed by Raman spectroscopy

Chemical physics letters, 1988-11, Vol.152 (4), p.319-324

1988

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Structure of all-trans-Retinal in the T1 State As Determined by Raman Spectroscopy: A Set of Carbon-Carbon and Carbon-Oxygen Stretching Force Constants Determined by the Normal Coordinate Analysis of the T1 Raman Lines of the Undeuterated and Variously Deuterated Retinals

Journal of physical chemistry (1952), 1995-05, Vol.99 (18), p.7160-7171

1995

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EFFECT OF PROTONATION ON THE ISOMERIZATION PROPERTIES OF n‐BUTYLAMINE SCHIFF BASE OF ISOMERIC RETINAL AS REVEALED BY DIRECT HPLC ANALYSES: SELECTION OF ISOMERIZATION PATHWAYS BY RETINAL PROTEINS

Photochemistry and photobiology, 1991-09, Vol.54 (3), p.433-443

1991

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Raman spectra of cis-trans isomers of retinal homologues. Key bands of unmethylated cis configurations and of all-trans parts of mono-cis isomers

Journal of Raman spectroscopy, 1986-10, Vol.17 (5), p.387-396

1986

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ZSTK474, a specific phosphatidylinositol 3-kinase inhibitor, induces G1 arrest of the cell cycle in vivo

Sequential Formation of Low-Mass Stars in the BRC 14 Region

Identification of candidate predictive markers of anticancer drug sensitivity using a panel of human cancer cell lines

Correlating Phosphatidylinositol 3-Kinase Inhibitor Efficacy with Signaling Pathway Status: In silico and Biological Evaluations

Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G0/G1 arrest

Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G{sub 0}/G{sub 1} arrest

Changes in Molecular Structure upon Triplet Excitation of All-trans-Spheroidene in n-Hexane Solution and 15-cis-Spheroidene Bound to the Photo-Reaction Center from Rhodobacter sphaeroides As Revealed by Resonance-Raman Spectroscopy and Normal-Coordinate Analysis

Abstract 4399: In vitro and in vivo evaluations of correlation between the activation status of signaling pathways and the efficacy of anticancer compounds in a panel of JFCR39 human cancer cell lines

Inhibition of PI3K by ZSTK474 suppressed tumor growth not via apoptosis but G 0/G 1 arrest

Abstract 2655: Visualization of G1 arrest of cell cycle induced by inhibition of PI-3 kinase in cancer cells: in vitro evaluations

Abstract C55: Efficacy of PI3K inhibitors to cancer cells with PIK3CA mutation or loss of PTEN expression

Vibronic Coupling through the In-Phase, CC Stretching Mode Plays a Major Role in the 2Ag - to 1Ag - Internal Conversion of all-trans-β-Carotene

Abstract 2493: Inhibition of phosphoinositide 3-kinase suppressed growth of cancer cells with PIK3CA mutations or loss of PTEN expression via G0/G1 arrest of cell cycle but not apoptosis

Picosecond time-resolved absorption study of all-trans- and 9-cis-retinal: configurational relaxation in the triplet state

Dependence of the triplet potential of retinal homologs on the chain length: resonance Raman spectroscopy and analysis of triplet-sensitized isomerization

EFFECT OF PROTONATION ON THE ISOMERIZATION PROPERTIES OF n-BUTYLAMINE SCHIFF BASE OF ISOMERIC RETINAL AS REVEALED BY DIRECT HPLC ANALYSES: SELECTION OF ISOMERIZATION PATHWAYS BY RETINAL PROTEINS

Transient Raman spectra of the all-trans and 7-, 9-, 11- and 13-mono-cis isomers of retinal and the mechanism of the cis-trans isomerization in the lowest excited triplet state

Vibronic Coupling through the In-Phase, CC Stretching Mode Plays a Major Role in the 2A g - to 1A g - Internal Conversion of all - trans -β-Carotene

COMPARISON OF THE PATHWAYS AND QUANTUM YIELDS OF DIRECT PHOTOISOMERIZATION OF UNPROTONATED AND PROTONATED N-BUTYLAMINE SCHIFF BASES OF ISOMERIC RETINYLIDENEACETALDEHYDE WITH THOSE OF SCHIFF BASES OF ISOMERIC RETINAL: RATIONALIZATION OF THE SELECTION OF THE RETINYLIDENE CHROMOPHORE BY RETINOCHROME

ISOMERIZATION OF THE RETINYLIDENE CHROMOPHORE OF BACTERIORHODOPSIN IN LIGHT ADAPTATION: INTRINSIC ISOMERIZATION OF THE CHROMOPHORE AND ITS CONTROL BY THE APO-PROTEIN

Changes in Molecular Structure upon Triplet Excitation of All-trans-Spheroidene in n-Hexane Solution and 15-cis-Spheroidene Bound to the Photo-Reaction Center from Rhodobacter s phaeroides As Revealed by Resonance-Raman Spectroscopy and Normal-Coordinate Analysis

Transient raman spectra of all-trans, 7-cis, 9-cis, 11-cis and 13-cis retinylideneacetaldehyde. Structures of triplet species as revealed by Raman spectroscopy

Structure of all-trans-Retinal in the T1 State As Determined by Raman Spectroscopy: A Set of Carbon-Carbon and Carbon-Oxygen Stretching Force Constants Determined by the Normal Coordinate Analysis of the T1 Raman Lines of the Undeuterated and Variously Deuterated Retinals

EFFECT OF PROTONATION ON THE ISOMERIZATION PROPERTIES OF n‐BUTYLAMINE SCHIFF BASE OF ISOMERIC RETINAL AS REVEALED BY DIRECT HPLC ANALYSES: SELECTION OF ISOMERIZATION PATHWAYS BY RETINAL PROTEINS

Raman spectra of cis-trans isomers of retinal homologues. Key bands of unmethylated cis configurations and of all-trans parts of mono-cis isomers

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