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Bivalent IAP antagonists, but not monovalent IAP antagonists, inhibit TNF-mediated NF- κ B signaling by degrading TRAF2-associated cIAP1 in cancer cells

Cell death discovery, 2017-01, Vol.3 (1), p.16046-16046, Article 16046

2017

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Activation of Akt2 Inhibits anoikis and apoptosis induced by myogenic differentiation

Cell death and differentiation, 2001-12, Vol.8 (12), p.1207-1212

2001

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Protein Kinase C Promotes Apoptosis in LNCaP Prostate Cancer Cells through Activation of p38 MAPK and Inhibition of the Akt Survival Pathway

The Journal of biological chemistry, 2003-09, Vol.278 (36), p.33753-33762

2003

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Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions

Carcinogenesis (New York), 2004-11, Vol.25 (11), p.2053-2059

2004

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Anti-Apoptotic Signaling by Hepatocyte Growth Factor/Met via the Phosphatidylinositol 3-Kinase/Akt and Mitogen-Activated Protein Kinase Pathways

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (1), p.247-252

2001

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Role of Steroid 11β-Hydroxylase and Steroid 18-Hydroxylase in the Biosynthesis of Glucocorticoids and Mineralocorticoids in Humans

Proceedings of the National Academy of Sciences - PNAS, 1992-02, Vol.89 (4), p.1458-1462

1992

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Adenoviral modification of mouse brain derived endothelial cells, bEnd3, to induce apoptosis by vascular endothelial growth factor

Oncogene, 2006-02, Vol.25 (6), p.954-958

2006

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Cell Cycle Withdrawal Promotes Myogenic Induction of Akt, a Positive Modulator of Myocyte Survival

Molecular and Cellular Biology, 1999-07, Vol.19 (7), p.5073-5082

1999

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AKT activation up-regulates insulin-like growth factor-I receptor expression and promotes invasiveness of human pancreatic cancer cells

Cancer research (Chicago, Ill.), 2001-01, Vol.120 (5), p.A39-A40

2001

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Growth inhibition and induction of apoptosis in mesothelioma cells by selenium and dependence on selenoprotein SEP15 genotype

Oncogene, 2004-06, Vol.23 (29), p.5032-5040

2004

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Identification of a chromosome 3p14.3-21.1 gene, APPL, encoding an adaptor molecule that interacts with the oncoprotein-serine/threonine kinase AKT2

Oncogene, 1999-09, Vol.18 (35), p.4891-4898

1999

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Congenitally Defective Aldosterone Biosynthesis in Humans: Inactivation of the P450C18 Gene (CYP11B2) Due to Nucleotide Deletion in CMO I-Deficient Patients

Biochemical and biophysical research communications, 1993-02, Vol.190 (3), p.864-869

1993

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Primary structure of human poly(ADP-ribose) synthetase as deduced from cDNA sequence

The Journal of biological chemistry, 1987-11, Vol.262 (33), p.15990-15997

1987

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Bivalent IAP antagonists, but not monovalent IAP antagonists, inhibit TNF-mediated NF-[kappa]B signaling by degrading TRAF2-associated cIAP1 in cancer cells

Cell death discovery, 2017-01, Vol.3, p.16046

2017

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Akt2 mRNA is highly expressed in embryonic brown fat and the AKT2 kinase is activated by insulin

Oncogene, 1998-05, Vol.16 (18), p.2407-2411

1998

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Translocation and activation of AKT2 in response to stimulation by insulin

Journal of cellular biochemistry, 1998-09, Vol.70 (4), p.433-441

1998

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Cloning and expression of A cDNA for human cytochrome P-450aldo as related to primary aldosteronism

Biochemical and biophysical research communications, 1990-11, Vol.173 (1), p.309-316

1990

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Cloning of cDNA and genomic DNA for human cytochrome P‐45011β

FEBS letters, 1990-09, Vol.269 (2), p.345-349

1990

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The Phosphatidylinositol 3-Kinase/AKT Signal Transduction Pathway Plays a Critical Role in the Expression of p21 super(WAF1/CIP1/SDI1) Induced by Cisplatin and Paclitaxel

Cancer research (Chicago, Ill.), 2000-10, Vol.60 (19), p.5390-5394

2000

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The phosphatidylinositol 3-kinase/AKT signal transduction pathway plays a critical role in the expression of p21WAF1/CIP1/SDI1 induced by cisplatin and paclitaxel

Cancer research (Chicago, Ill.), 2000-10, Vol.60 (19), p.5390-5394

2000

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A nonsense mutation (TGG [Trp116] → TAG [stop]) in CYP11B1 causes steroid 11β-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1993-12, Vol.77 (6), p.1677-1682

1993

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Congenitally defective aldosterone biosynthesis in humans : inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients

Biochemical and biophysical research communications, 1993-02, Vol.190 (3), p.864-869

1993

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Congenitally defective aldosterone biosynthesis in humans : the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients

Biochemical and biophysical research communications, 1992-01, Vol.182 (2), p.974-979

1992

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The chimeric gene linked to glucocorticoid-suppressible hyperaldosteronism encodes a fused P-450 protein possessing aldosterone synthase activity

Biochemical and biophysical research communications, 1992-12, Vol.189 (2), p.885-891

1992

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Cytogenetics and molecular genetics of lung cancer

American journal of medical genetics, 2002-10, Vol.115 (3), p.183-188

2002

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Bivalent IAP antagonists, but not monovalent IAP antagonists, inhibit TNF-mediated NF- κ B signaling by degrading TRAF2-associated cIAP1 in cancer cells

Activation of Akt2 Inhibits anoikis and apoptosis induced by myogenic differentiation

Protein Kinase C Promotes Apoptosis in LNCaP Prostate Cancer Cells through Activation of p38 MAPK and Inhibition of the Akt Survival Pathway

Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions

Anti-Apoptotic Signaling by Hepatocyte Growth Factor/Met via the Phosphatidylinositol 3-Kinase/Akt and Mitogen-Activated Protein Kinase Pathways

Role of Steroid 11β-Hydroxylase and Steroid 18-Hydroxylase in the Biosynthesis of Glucocorticoids and Mineralocorticoids in Humans

Adenoviral modification of mouse brain derived endothelial cells, bEnd3, to induce apoptosis by vascular endothelial growth factor

Cell Cycle Withdrawal Promotes Myogenic Induction of Akt, a Positive Modulator of Myocyte Survival

AKT activation up-regulates insulin-like growth factor-I receptor expression and promotes invasiveness of human pancreatic cancer cells

Growth inhibition and induction of apoptosis in mesothelioma cells by selenium and dependence on selenoprotein SEP15 genotype

Identification of a chromosome 3p14.3-21.1 gene, APPL, encoding an adaptor molecule that interacts with the oncoprotein-serine/threonine kinase AKT2

Congenitally Defective Aldosterone Biosynthesis in Humans: Inactivation of the P450C18 Gene (CYP11B2) Due to Nucleotide Deletion in CMO I-Deficient Patients

Primary structure of human poly(ADP-ribose) synthetase as deduced from cDNA sequence

Bivalent IAP antagonists, but not monovalent IAP antagonists, inhibit TNF-mediated NF-[kappa]B signaling by degrading TRAF2-associated cIAP1 in cancer cells

Akt2 mRNA is highly expressed in embryonic brown fat and the AKT2 kinase is activated by insulin

Translocation and activation of AKT2 in response to stimulation by insulin

Cloning and expression of A cDNA for human cytochrome P-450aldo as related to primary aldosteronism

Cloning of cDNA and genomic DNA for human cytochrome P‐45011β

The Phosphatidylinositol 3-Kinase/AKT Signal Transduction Pathway Plays a Critical Role in the Expression of p21 super(WAF1/CIP1/SDI1) Induced by Cisplatin and Paclitaxel

The phosphatidylinositol 3-kinase/AKT signal transduction pathway plays a critical role in the expression of p21WAF1/CIP1/SDI1 induced by cisplatin and paclitaxel

A nonsense mutation (TGG [Trp116] → TAG [stop]) in CYP11B1 causes steroid 11β-hydroxylase deficiency

Congenitally defective aldosterone biosynthesis in humans : inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients

Congenitally defective aldosterone biosynthesis in humans : the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients

The chimeric gene linked to glucocorticoid-suppressible hyperaldosteronism encodes a fused P-450 protein possessing aldosterone synthase activity

Cytogenetics and molecular genetics of lung cancer

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