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Over-expression of insulin-like growth factor binding protein-related protein-1(IGFBP-rP1/mac25) in the M12 prostate cancer cell line alters tumor growth by a delay in G1 and cyclin A associated apoptosis

Publication ,  Journal Article
Sprenger, CC; Vail, ME; Evans, K; Simurdak, J; Plymate, SR
Published in: Oncogene
January 3, 2002

Duke Scholars

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Published In

Oncogene

DOI

EISSN

1476-5594

ISSN

0950-9232

Publication Date

January 3, 2002

Volume

21

Issue

1

Start / End Page

140 / 147

Publisher

Springer Science and Business Media LLC

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences
 

Citation

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Sprenger, C. C., Vail, M. E., Evans, K., Simurdak, J., & Plymate, S. R. (2002). Over-expression of insulin-like growth factor binding protein-related protein-1(IGFBP-rP1/mac25) in the M12 prostate cancer cell line alters tumor growth by a delay in G1 and cyclin A associated apoptosis. Oncogene, 21(1), 140–147. https://doi.org/10.1038/sj.onc.1205021
Sprenger, Cynthia C., Mary E. Vail, Karen Evans, Jerry Simurdak, and Stephen R. Plymate. “Over-expression of insulin-like growth factor binding protein-related protein-1(IGFBP-rP1/mac25) in the M12 prostate cancer cell line alters tumor growth by a delay in G1 and cyclin A associated apoptosis.” Oncogene 21, no. 1 (January 3, 2002): 140–47. https://doi.org/10.1038/sj.onc.1205021.
Sprenger, Cynthia C., et al. “Over-expression of insulin-like growth factor binding protein-related protein-1(IGFBP-rP1/mac25) in the M12 prostate cancer cell line alters tumor growth by a delay in G1 and cyclin A associated apoptosis.” Oncogene, vol. 21, no. 1, Springer Science and Business Media LLC, Jan. 2002, pp. 140–47. Crossref, doi:10.1038/sj.onc.1205021.

Published In

Oncogene

DOI

EISSN

1476-5594

ISSN

0950-9232

Publication Date

January 3, 2002

Volume

21

Issue

1

Start / End Page

140 / 147

Publisher

Springer Science and Business Media LLC

Related Subject Headings

  • Oncology & Carcinogenesis
  • 1112 Oncology and Carcinogenesis
  • 1103 Clinical Sciences