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[HTML][HTML] Small molecule NSC1892 targets the CUL4A/4B-DDB1 interactions and causes impairment of CRL4DCAF4 E3 ligases to inhibit colorectal cancer cell growth

C Yang, J Wu, H He, H Liu - International Journal of Biological …, 2020 - ncbi.nlm.nih.gov
Abstract Cullin 4A and 4B (CUL4A and 4B) function as oncogenes in colorectal cancer
(CRC) cells. Both of them conservatively associate with DNA damage-binding protein 1 …
被引用次数：8 相关文章
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[HTML][HTML] Small molecule NSC1892 targets the CUL4A/4B-DDB1 interactions and causes impairment of CRL4DCAF4 E3 ligases to inhibit colorectal cancer cell growth

C Yang, J Wu, H He, H Liu - International Journal of Biological Sciences, 2020 - ijbs.com
Abstract Cullin 4A and 4B (CUL4A and 4B) function as oncogenes in colorectal cancer
(CRC) cells. Both of them conservatively associate with DNA damage–binding protein 1 …

Small molecule NSC1892 targets the CUL4A/4B-DDB1 interactions and causes impairment of CRL4DCAF4 E3 ligases to inhibit colorectal cancer cell growth

C Yang, J Wu, H He, H Liu - International journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
Cullin 4A and 4B (CUL4A and 4B) function as oncogenes in colorectal cancer (CRC) cells.
Both of them conservatively associate with DNA damage-binding protein 1 (DDB1) and …

Small molecule NSC1892 targets the CUL4A/4B-DDB1 interactions and causes impairment of CRL4DCAF4 E3 ligases to inhibit colorectal cancer cell growth.

C Yang, J Wu, H He, H Liu - International Journal of Biological …, 2020 - europepmc.org
Abstract Cullin 4A and 4B (CUL4A and 4B) function as oncogenes in colorectal cancer
(CRC) cells. Both of them conservatively associate with DNA damage-binding protein 1 …
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[PDF][PDF] Small molecule NSC1892 targets the CUL4A/4B-DDB1 interactions and causes impairment of CRL4DCAF4 E3 ligases to inhibit colorectal cancer cell growth

C Yang, J Wu, H He, H Liu - International Journal of …, 2020 - pdfs.semanticscholar.org
Abstract Cullin 4A and 4B (CUL4A and 4B) function as oncogenes in colorectal cancer
(CRC) cells. Both of them conservatively associate with DNA damage–binding protein 1 …