A third transactivation function (AF3) of human progesterone receptors located in the unique N-terminal segment of the B-isoform.
about
CUE domain containing 2 regulates degradation of progesterone receptor by ubiquitin-proteasomeA functional polymorphism in the promoter of the progesterone receptor gene associated with endometrial cancer risk.Jun dimerization protein 2 functions as a progesterone receptor N-terminal domain coactivator.GCUNC-45 is a novel regulator for the progesterone receptor/hsp90 chaperoning pathway.The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor bindingCyclin dependent kinase 2 and the regulation of human progesterone receptor activityThe progesterone receptor Val660-->Leu polymorphism and breast cancer risk.Expression and transcriptional activity of progesterone receptor A and progesterone receptor B in mammalian cellsThe progestational and androgenic properties of medroxyprogesterone acetate: gene regulatory overlap with dihydrotestosterone in breast cancer cells.Post-translational modifications of the progesterone receptorsDetection of progesterone receptor forms A and B by immunohistochemical analysisSteroid receptor coactivator-1 from brain physically interacts differentially with steroid receptor subtypesSteroid receptor coactivator-2 expression in brain and physical associations with steroid receptorsAffinity of estrogens for human progesterone receptor A and B monomers and risk of breast cancer: a comparative molecular modeling studyThe human progesterone receptor shows evidence of adaptive evolution associated with its ability to act as a transcription factorTwo domains of the progesterone receptor interact with the estrogen receptor and are required for progesterone activation of the c-Src/Erk pathway in mammalian cellsMolecular Signaling of Progesterone, Growth Hormone, Wnt, and HER in Mammary Glands of Dogs, Rodents, and Humans: New Treatment Target Identification.Progesterone action in human tissues: regulation by progesterone receptor (PR) isoform expression, nuclear positioning and coregulator expression.Na(+) and K(+) allosterically regulate cooperative DNA binding by the human progesterone receptorMinireview: Progesterone Regulation of Proliferation in the Normal Human Breast and in Breast Cancer: A Tale of Two Scenarios?Selective interactions of Kruppel-like factor 9/basic transcription element-binding protein with progesterone receptor isoforms A and B determine transcriptional activity of progesterone-responsive genes in endometrial epithelial cells.Progesterone receptors, their isoforms and progesterone regulated transcriptionProgestogens used in postmenopausal hormone therapy: differences in their pharmacological properties, intracellular actions, and clinical effectsCytokine and progesterone receptor interplay in the regulation of MUC1 gene expression.Role of nuclear progesterone receptor isoforms in uterine pathophysiology.Heregulin induces transcriptional activation of the progesterone receptor by a mechanism that requires functional ErbB-2 and mitogen-activated protein kinase activation in breast cancer cells.Genomics of preterm birth.PIAS3 induction of PRB sumoylation represses PRB transactivation by destabilizing its retention in the nucleusProgesterone receptor signaling in the initiation of pregnancy and preservation of a healthy uterus.Ulipristal Acetate Inhibits Progesterone Receptor Isoform A-Mediated Human Breast Cancer Proliferation and BCl2-L1 Expression.Thermodynamic analysis of progesterone receptor-promoter interactions reveals a molecular model for isoform-specific function.Conserved steroid hormone homology converges on nuclear factor κB to modulate inflammation in asthma.Estradiol Preferentially Induces Progestin Receptor-A (PR-A) Over PR-B in Cells Expressing Nuclear Receptor Coactivators in the Female Mouse Hypothalamus(1,2,3).The progesterone receptor regulates implantation, decidualization, and glandular development via a complex paracrine signaling network.Thermodynamic dissection of estrogen receptor-promoter interactions reveals that steroid receptors differentially partition their self-association and promoter binding energetics.Inhibitory cross-talk between steroid hormone receptors: differential targeting of estrogen receptor in the repression of its transcriptional activity by agonist- and antagonist-occupied progestin receptors.p38 and p42/44 MAPKs differentially regulate progesterone receptor A and B isoform stabilization.Progestin receptor subtypes in the brain: the known and the unknownMolecular evidence of functional progesterone withdrawal in human myometrium.Differential and interactive effects of ligand-bound progesterone receptor A and B isoforms on tyrosine hydroxylase promoter activity.
P2860
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P2860
A third transactivation function (AF3) of human progesterone receptors located in the unique N-terminal segment of the B-isoform.
description
1994 nî lūn-bûn
@nan
1994 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
A third transactivation functi ...... inal segment of the B-isoform.
@ast
A third transactivation functi ...... inal segment of the B-isoform.
@en
type
label
A third transactivation functi ...... inal segment of the B-isoform.
@ast
A third transactivation functi ...... inal segment of the B-isoform.
@en
prefLabel
A third transactivation functi ...... inal segment of the B-isoform.
@ast
A third transactivation functi ...... inal segment of the B-isoform.
@en
P2093
P356
P1476
A third transactivation functi ...... inal segment of the B-isoform.
@en
P2093
Horwitz KB
Hovland AR
Melville MY
Sartorius CA
Takimoto GS
P304
P356
10.1210/ME.8.10.1347
P577
1994-10-01T00:00:00Z