Nuclear translocation of the 1,25D3-MARRS (membrane associated rapid response to steroids) receptor protein and NFkappaB in differentiating NB4 leukemia cells. (Q43197595)

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scientific article published on 11 January 2010

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English	Nuclear translocation of the 1,25D3-MARRS (membrane associated rapid response to steroids) receptor protein and NFkappaB in differentiating NB4 leukemia cells.	scientific article published on 11 January 2010

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16 January 2020

Nuclear translocation of the 1,25D3-MARRS (membrane associated rapid response to steroids) receptor protein and NFkappaB in differentiating NB4 leukemia cells (English)

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16 January 2020

Mary C Farach-Carson

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16 January 2020

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Wenqing Wu

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16 January 2020

Greg Beilhartz

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16 January 2020

Yvette Roy

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16 January 2020

Cynthia L Richard

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16 January 2020

Maureen Curtin

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16 January 2020

Lauren Brown

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16 January 2020

Danielle Cadieux

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16 January 2020

Marc Coppolino

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16 January 2020

Ilka Nemere

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16 January 2020

Kelly A Meckling

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16 January 2020

Experimental Cell Research

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16 January 2020

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16 January 2020

1101-1108

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16 January 2020

Signaling pathways in the differentiation therapy for acute promyelocytic leukemia

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7 January 2021

1alpha,25-dihydroxyvitamin D3 and bryostatin-1 synergize to induce monocytic differentiation of NB4 acute promyelocytic leukemia cells by modulating cell cycle progression

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Membrane receptors for vitamin D steroid hormones: potential new drug targets.

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Immunochemical studies on the putative plasmalemmal receptor for 1, 25-dihydroxyvitamin D(3). III. Vitamin D status

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Nonnuclear effects of the steroid hormone 1 alpha,25(OH)2-vitamin D3: analogs are able to functionally differentiate between nuclear and membrane receptors

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1,25-(OH)2D3 modulates growth plate chondrocytes via membrane receptor-mediated protein kinase C by a mechanism that involves changes in phospholipid metabolism and the action of arachidonic acid and PGE2.

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7 January 2021

Vitamin D3 metabolites regulate LTBP1 and latent TGF-beta1 expression and latent TGF-beta1 incorporation in the extracellular matrix of chondrocytes

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7 January 2021

Identification and characterization of 1,25D3-membrane-associated rapid response, steroid (1,25D3-MARRS) binding protein

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The 1,25D3-MARRS protein: contribution to steroid stimulated calcium uptake in chicks and rats

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Regulation of expression of 1,25D3-MARRS/ERp57/PDIA3 in rat IEC-6 cells by TGF beta and 1,25(OH)2D3.

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Ribozyme knockdown functionally links a 1,25(OH)2D3 membrane binding protein (1,25D3-MARRS) and phosphate uptake in intestinal cells.

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7 January 2021

Regulation of growth plate chondrocytes by 1,25-dihydroxyvitamin D3 requires caveolae and caveolin-1.

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Nuclear localization and DNA interaction of protein disulfide isomerase ERp57 in mammalian cells.

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DNA-binding activity of the ERp57 C-terminal domain is related to a redox-dependent conformational change

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The DNA-binding activity of protein disulfide isomerase ERp57 is associated with the a(') domain.

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1,25-Dihydroxyvitamin D3 stimulates expression and translocation of protein kinase Calpha and Cdelta via a nongenomic mechanism and rapidly induces phosphorylation of a 33-kDa protein in acute promyelocytic NB4 cells

1 reference

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1alpha,25-dihydroxyvitamin D3 stimulates phosphorylation of IkappaBalpha and synergizes with TPA to induce nuclear translocation of NFkappaB during monocytic differentiation of NB4 leukemia cells

1 reference

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1,25-dihydroxyvitamin D3 primes acute promyelocytic cells for TPA-induced monocytic differentiation through both PKC and tyrosine phosphorylation cascades.

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Identification and characterization of 1,25D3-membrane-associated rapid response, steroid (1,25D3-MARRS)-binding protein in rat IEC-6 cells

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The ERp57/GRp58/1,25D3-MARRS receptor: multiple functional roles in diverse cell systems

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1 beta, 25 (OH)2-vitamin D3 is an antagonist of 1 alpha,25 (OH)2-vitamin D3 stimulated transcaltachia (the rapid hormonal stimulation of intestinal calcium transport)

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Protein disulfide isomerase serves as a molecular chaperone to maintain estrogen receptor alpha structure and function.

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