Trophic effect in MCF-7 cells of ERα17p, a peptide corresponding to a platform regulatory motif of the estrogen receptor α—Underlying mechanisms-Reference-Cited by-同舟云学术

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Trophic effect in MCF-7 cells of ERα17p, a peptide corresponding to a platform regulatory motif of the estrogen receptor α—Underlying mechanisms

Published:2008-03 Issue:1-2 Volume:109 Page:138-149
ISSN:0960-0760
Container-title:The Journal of Steroid Biochemistry and Molecular Biology
language:en
Short-container-title:The Journal of Steroid Biochemistry and Molecular Biology

Author:

Gallo Dominique,Haddad Iman,Duvillier Hugues,Jacquemotte Françoise,Laïos Ioanna,Laurent Guy,Jacquot Yves,Vinh Joëlle,Leclercq Guy

Publisher

Elsevier BV

Subject

Cell Biology,Clinical Biochemistry,Endocrinology,Molecular Biology,Molecular Medicine,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference70 articles.

1. Functional domains of the human estrogen receptor;Kumar;Cell,1987

2. The hormone-binding domains of the estrogen and glucocorticoid receptors contain an inducible transcription activation function;Webster;Cell,1988

3. The human estrogen receptor has two independent nonacidic transcriptional activation functions;Tora;Cell,1989

4. Identification of a third autonomous activation domain within the human estrogen receptor;Norris;Mol. Endocrinol.,1997

5. Differential ligand activation of estrogen receptors ERalpha and ERbeta at AP1 sites;Paech;Science,1997

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1. Antagonism of Estrogen Receptor α-Driven Transcription Mediated by AP-1 in Breast Cancer Therapy;Endocrines;2024-03-06

2. Promising Perspectives of the Antiproliferative GPER Inverse Agonist ERα17p in Breast Cancer;Cells;2023-02-18

3. Identification of a human estrogen receptor α tetrapeptidic fragment with dual antiproliferative and anti-nociceptive action;Scientific Reports;2023-01-24

4. Importins involved in the nuclear transportation of steroid hormone receptors: In silico and in vitro data;Frontiers in Endocrinology;2022-09-06

5. Deciphering of a Putative GPER Recognition Domain in ERα and ERα36;Frontiers in Endocrinology;2022-06-30

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