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Author Correction: Akt2 knock-down reveals its contribution to human lung cancer cell proliferation, growth, motility, invasion and endothelial cell tube formation

Scientific reports, 2022-06, Vol.12 (1), p.10431-10431, Article 10431

2022

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Estrogen Induction of the Cyclin D1 Promoter: Involvement of a cAMP Response-Like Element

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (20), p.11217-11222

1999

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Frondoside A inhibits human breast cancer cell survival, migration, invasion and the growth of breast tumor xenografts

European journal of pharmacology, 2011-10, Vol.668 (1-2), p.25-34

2011

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Captopril as a Potential Inhibitor of Lung Tumor Growth and Metastasis

Annals of the New York Academy of Sciences, 2008-09, Vol.1138 (1), p.65-72

2008

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Ligand-free estrogen receptor activity complements IGF1R to induce the proliferation of the MCF-7 breast cancer cells

BMC cancer, 2012-07, Vol.12 (1), p.291-291, Article 291

2012

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Structure, Synthesis, and Molecular Cloning of Dermaseptins B, a Family of Skin Peptide Antibiotics

The Journal of biological chemistry, 1998-06, Vol.273 (24), p.14690-14697

1998

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Akt2 knock-down reveals its contribution to human lung cancer cell proliferation, growth, motility, invasion and endothelial cell tube formation

Scientific reports, 2015-08, Vol.5 (1), p.12759-12759, Article 12759

2015

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Direct Inhibition of the Expression of Cyclin D1 Gene by Sodium Butyrate

Biochemical and biophysical research communications, 1996-12, Vol.229 (1), p.163-169

1996

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p21WAF1/CIP1 Selectively Controls the Transcriptional Activity of Estrogen Receptor α

Molecular and Cellular Biology, 2005-03, Vol.25 (6), p.2419-2430

2005

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Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development

The journal of clinical endocrinology and metabolism, 2009-10, Vol.94 (10), p.3913-3921

2009

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Sodium Butyrate Induces G2 Arrest in the Human Breast Cancer Cells MDA-MB-231 and Renders Them Competent for DNA Rereplication

Experimental cell research, 1999-03, Vol.247 (2), p.432-440

1999

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B-ind1, a Novel Mediator of Rac1 Signaling Cloned from Sodium Butyrate-treated Fibroblasts

The Journal of biological chemistry, 2000-06, Vol.275 (23), p.17344-17348

2000

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The c-kit tyrosine kinase inhibitor STI571 for colorectal cancer therapy

Cancer research (Chicago, Ill.), 2002-09, Vol.62 (17), p.4879-4883

2002

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Geldanamycin, an inhibitor of the chaperone activity of HSP90, induces MAPK‐independent cell cycle arrest

International journal of cancer, 2004-05, Vol.109 (5), p.643-652

2004

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Cellular effects of purvalanol A: A specific inhibitor of cyclin‐dependent kinase activities

International journal of cancer, 2002-02, Vol.97 (6), p.761-769

2002

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Mitogenic Activity of Estrogens in Human Breast Cancer Cells Does Not Rely on Direct Induction of Mitogen-Activated Protein Kinase/Extracellularly Regulated Kinase or Phosphatidylinositol 3-Kinase

Molecular endocrinology (Baltimore, Md.), 2004-11, Vol.18 (11), p.2700-2713

2004

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Indirect participation of Hsp90 in the regulation of the cyclin E turnover

Biochemical pharmacology, 2009-01, Vol.77 (2), p.151-158

2009

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p21 super(WAF1/CIP1) Selectively Controls the Transcriptional Activity of Estrogen Receptor alpha

Molecular and cellular biology, 2005-03, Vol.25 (6), p.2419-2430

2005

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p21 WAF1/CIP1 Selectively Controls the Transcriptional Activity of Estrogen Receptor α

Molecular and cellular biology, 2005-03, Vol.25 (6), p.2419-2430

2005

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Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development

Molecular endocrinology (Baltimore, Md.), 2009-11, Vol.23 (11), p.1936-1936

2009

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Transcriptional activation by the oestrogen receptor α is modulated through inhibition of cyclin-dependent kinases

Oncogene, 2002-08, Vol.21 (37), p.5773-5782

2002

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Transcriptional activation by the oestrogen receptor [alpha] is modulated through inhibition of cyclin-dependent kinases

Oncogene, 2002-08, Vol.21 (37), p.5773

2002

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Rapamycin inhibits cdk4 activation, p 21WAF1/CIP1 expression and G1‐phase progression in transformed mouse fibroblasts

International journal of cancer, 2004-01, Vol.108 (2), p.200-206

2004

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Rapamycin inhibits cdk4 activation, p 21(WAF1/CIP1) expression and G1-phase progression in transformed mouse fibroblasts

International journal of cancer, 2004-01, Vol.108 (2), p.200-206

2004

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Rapamycin inhibits cdk4 activation, p 21 WAF1/CIP1 expression and G1‐phase progression in transformed mouse fibroblasts

International journal of cancer, 2004-01, Vol.108 (2), p.200-206

2004

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Author Correction: Akt2 knock-down reveals its contribution to human lung cancer cell proliferation, growth, motility, invasion and endothelial cell tube formation

Estrogen Induction of the Cyclin D1 Promoter: Involvement of a cAMP Response-Like Element

Frondoside A inhibits human breast cancer cell survival, migration, invasion and the growth of breast tumor xenografts

Captopril as a Potential Inhibitor of Lung Tumor Growth and Metastasis

Ligand-free estrogen receptor activity complements IGF1R to induce the proliferation of the MCF-7 breast cancer cells

Structure, Synthesis, and Molecular Cloning of Dermaseptins B, a Family of Skin Peptide Antibiotics

Akt2 knock-down reveals its contribution to human lung cancer cell proliferation, growth, motility, invasion and endothelial cell tube formation

Direct Inhibition of the Expression of Cyclin D1 Gene by Sodium Butyrate

p21WAF1/CIP1 Selectively Controls the Transcriptional Activity of Estrogen Receptor α

Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development

Sodium Butyrate Induces G2 Arrest in the Human Breast Cancer Cells MDA-MB-231 and Renders Them Competent for DNA Rereplication

B-ind1, a Novel Mediator of Rac1 Signaling Cloned from Sodium Butyrate-treated Fibroblasts

The c-kit tyrosine kinase inhibitor STI571 for colorectal cancer therapy

Geldanamycin, an inhibitor of the chaperone activity of HSP90, induces MAPK‐independent cell cycle arrest

Cellular effects of purvalanol A: A specific inhibitor of cyclin‐dependent kinase activities

Mitogenic Activity of Estrogens in Human Breast Cancer Cells Does Not Rely on Direct Induction of Mitogen-Activated Protein Kinase/Extracellularly Regulated Kinase or Phosphatidylinositol 3-Kinase

Indirect participation of Hsp90 in the regulation of the cyclin E turnover

p21 super(WAF1/CIP1) Selectively Controls the Transcriptional Activity of Estrogen Receptor alpha

p21 WAF1/CIP1 Selectively Controls the Transcriptional Activity of Estrogen Receptor α

Partial Primary Deficiency of Insulin-Like Growth Factor (IGF)-I Activity Associated with IGF1 Mutation Demonstrates Its Critical Role in Growth and Brain Development

Transcriptional activation by the oestrogen receptor α is modulated through inhibition of cyclin-dependent kinases

Transcriptional activation by the oestrogen receptor [alpha] is modulated through inhibition of cyclin-dependent kinases

Rapamycin inhibits cdk4 activation, p 21WAF1/CIP1 expression and G1‐phase progression in transformed mouse fibroblasts

Rapamycin inhibits cdk4 activation, p 21(WAF1/CIP1) expression and G1-phase progression in transformed mouse fibroblasts

Rapamycin inhibits cdk4 activation, p 21 WAF1/CIP1 expression and G1‐phase progression in transformed mouse fibroblasts

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