Gap-junctional communication in normal and neoplastic prostate epithelial cells and its regulation by cAMP. (Q34371624)

1 August 2017

title

Gap-junctional communication in normal and neoplastic prostate epithelial cells and its regulation by cAMP. (English)

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1 August 2017

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Mehta PP

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1 August 2017

Lokeshwar BL

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1 August 2017

Schiller PC

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1 August 2017

Bendix MV

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1 August 2017

Ostenson RC

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1 August 2017

Howard GA

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1 August 2017

Roos BA

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1 August 2017

publication date

1 January 1996

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1 August 2017

published in

Molecular Carcinogenesis

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1 August 2017

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1 August 2017

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1 August 2017

page(s)

18-32

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describes a project that uses

1 August 2017

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Metabolic Coupling, Ionic Coupling and Cell Contacts

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Gap junctions: new tools, new answers, new questions

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Gap junctional intercellular communication and carcinogenesis

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Transcription of the gene for the gap junctional protein connexin43 and expression of functional cell-to-cell channels are regulated by cAMP.

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The hormone-induced regulation of contact-dependent cell-cell communication by phosphorylation

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Human primary prostate tumor cell line, ALVA‐31: A new model for studying the hormonal regulation of prostate tumor cell growth

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IGF-binding proteins in human prostate tumor cells: expression and regulation by 1,25-dihydroxyvitamin D3.

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Effects of sex hormone binding globulin (SHBG) on human prostatic carcinoma

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Connexin43: a protein from rat heart homologous to a gap junction protein from liver

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Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA

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Turnover and phosphorylation dynamics of connexin43 gap junction protein in cultured cardiac myocytes.

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Phorbol ester induces phosphorylation and down-regulation of connexin 43 in WB cells

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Modulation of gap junction transcript and protein expression during pregnancy in the rat

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Growth factors modulate junctional cell-to-cell communication

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Altered regulation of intercellular communication by epidermal growth factor, transforming growth factor-beta and peptide hormones in normal human keratinocytes

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Inhibition of Glycosylation Induces Formation of Open Connexin-43 Cell-to-Cell Channels and Phosphorylation and Triton X-100 Insolubility of Connexin-43

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10.1002/(SICI)1098-2744(199601)15:1<18::AID-MC4>3.0.CO;2-O

21 January 2018

Identifiers

DOI

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1 August 2017

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