D J Schroen - JoVE Visualize

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Journal of Cellular Physiology|November 1, 1996

Inhibition of rabbit collagenase (matrix metalloproteinase-1; MMP-1) transcription by retinoid receptors: evidence for binding of RARs/RXRs to the -77 AP-1 site through interactions with c-JunD J Schroen, C E Brinckerhoff

Cellular Immunology|January 10, 1996

Interaction of mouse thymocytes and a thymocyte-like cell line with the ECM glycoprotein entactinD J Schroen, H T Cheung

Gene Expression|January 1, 1996

Nuclear hormone receptors inhibit matrix metalloproteinase (MMP) gene expression through diverse mechanismsD J Schroen, C E Brinckerhoff

Journal of Immunological Methods|April 15, 1994

An adhesion assay using minimal shear force to remove nonadherent cellsJ J St John, D J Schroen, H T Cheung

Molecular Endocrinology (Baltimore, Md.)|February 12, 1998

Characterization of receptor interaction and transcriptional repression by the corepressor SMRTH Li, C Leo, D J Schroen, et al.

Biochemical and Biophysical Research Communications|August 8, 1997

The nuclear receptor corepressor SMRT inhibits interstitial collagenase (MMP-1) transcription through an HRE-independent mechanismD J Schroen, J D Chen, M P Vincenti, et al.

Molecular Carcinogenesis|April 16, 1998

v-src activation of the collagenase-1 (matrix metalloproteinase-1) promoter through PEA3 and STAT: requirement of extracellular signal-regulated kinases and inhibition by retinoic acid receptorsM P Vincenti, D J Schroen, C I Coon, et al.

Critical Reviews in Eukaryotic Gene Expression|January 1, 1996

Regulating expression of the gene for matrix metalloproteinase-1 (collagenase): mechanisms that control enzyme activity, transcription, and mRNA stabilityM P Vincenti, L A White, D J Schroen, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999

SMRTe, a silencing mediator for retinoid and thyroid hormone receptors-extended isoform that is more related to the nuclear receptor corepressorE J Park, D J Schroen, M Yang, et al.

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Showing results (1-10 of 9) with videos related to

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Pageof 1

Journal of Cellular Physiology|November 1, 1996

Inhibition of rabbit collagenase (matrix metalloproteinase-1; MMP-1) transcription by retinoid receptors: evidence for binding of RARs/RXRs to the -77 AP-1 site through interactions with c-JunD J Schroen, C E Brinckerhoff

Cellular Immunology|January 10, 1996

Interaction of mouse thymocytes and a thymocyte-like cell line with the ECM glycoprotein entactinD J Schroen, H T Cheung

Gene Expression|January 1, 1996

Nuclear hormone receptors inhibit matrix metalloproteinase (MMP) gene expression through diverse mechanismsD J Schroen, C E Brinckerhoff

Journal of Immunological Methods|April 15, 1994

An adhesion assay using minimal shear force to remove nonadherent cellsJ J St John, D J Schroen, H T Cheung

Molecular Endocrinology (Baltimore, Md.)|February 12, 1998

Characterization of receptor interaction and transcriptional repression by the corepressor SMRTH Li, C Leo, D J Schroen, et al.

Biochemical and Biophysical Research Communications|August 8, 1997

The nuclear receptor corepressor SMRT inhibits interstitial collagenase (MMP-1) transcription through an HRE-independent mechanismD J Schroen, J D Chen, M P Vincenti, et al.

Molecular Carcinogenesis|April 16, 1998

v-src activation of the collagenase-1 (matrix metalloproteinase-1) promoter through PEA3 and STAT: requirement of extracellular signal-regulated kinases and inhibition by retinoic acid receptorsM P Vincenti, D J Schroen, C I Coon, et al.

Critical Reviews in Eukaryotic Gene Expression|January 1, 1996

Regulating expression of the gene for matrix metalloproteinase-1 (collagenase): mechanisms that control enzyme activity, transcription, and mRNA stabilityM P Vincenti, L A White, D J Schroen, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999

SMRTe, a silencing mediator for retinoid and thyroid hormone receptors-extended isoform that is more related to the nuclear receptor corepressorE J Park, D J Schroen, M Yang, et al.

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