Erratum to: A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1475-2867

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Erratum to: A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy ; volume:10 ; number:1 ; day:28 ; month:10 ; year:2010 ; pages:1 ; date:12.2010
Cancer cell international ; 10, Heft 1 (28.10.2010), 1, 12.2010

Creator: Cheung, Chun Hei Antonio

Contributor: Sun, Xueying
Kanwar, Jagat R.
Bai, Ji-Zhong
Cheng, LiTing
Krissansen, Geoffrey W.
SpringerLink (Online service)

DOI: 10.1186/1475-2867-10-43

URN: urn:nbn:de:1111-2016073016094

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

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Cheung, Chun Hei Antonio
Sun, Xueying
Kanwar, Jagat R.
Bai, Ji-Zhong
Cheng, LiTing
Krissansen, Geoffrey W.
SpringerLink (Online service)

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A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

Survivin gene silencing sensitizes prostate cancer cells to selenium growth inhibition

miR-494 Sensitizes Gastric Cancer Cells to TRAIL Treatment Through Downregulation of Survivin

Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin

Albendazole sensitizes cancer cells to ionizing radiation

Hsp90 inhibition sensitizes DLBCL cells to cisplatin

Localization matters: nuclear-trapped Survivin sensitizes glioblastoma cells to temozolomide by elevating cellular senescence and impairing homologous recombination

FK228 sensitizes radioresistant small cell lung cancer cells to radiation

Letrozole sensitizes breast cancer cells to ionizing radiation

HMGN1 loss sensitizes lung cancer cells to chemotherapy

ALDH1-mediated autophagy sensitizes glioblastoma cells to ferroptosis

ALDH1A inhibition sensitizes colon cancer cells to chemotherapy

A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

Survivin gene silencing sensitizes prostate cancer cells to selenium growth inhibition

miR-494 Sensitizes Gastric Cancer Cells to TRAIL Treatment Through Downregulation of Survivin

Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin

Albendazole sensitizes cancer cells to ionizing radiation

Hsp90 inhibition sensitizes DLBCL cells to cisplatin

Localization matters: nuclear-trapped Survivin sensitizes glioblastoma cells to temozolomide by elevating cellular senescence and impairing homologous recombination

FK228 sensitizes radioresistant small cell lung cancer cells to radiation

Letrozole sensitizes breast cancer cells to ionizing radiation

HMGN1 loss sensitizes lung cancer cells to chemotherapy

ALDH1-mediated autophagy sensitizes glioblastoma cells to ferroptosis

ALDH1A inhibition sensitizes colon cancer cells to chemotherapy

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Erratum to: A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

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Other Objects (12)

A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

Survivin gene silencing sensitizes prostate cancer cells to selenium growth inhibition

miR-494 Sensitizes Gastric Cancer Cells to TRAIL Treatment Through Downregulation of Survivin

Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin

Albendazole sensitizes cancer cells to ionizing radiation

Hsp90 inhibition sensitizes DLBCL cells to cisplatin

Localization matters: nuclear-trapped Survivin sensitizes glioblastoma cells to temozolomide by elevating cellular senescence and impairing homologous recombination

FK228 sensitizes radioresistant small cell lung cancer cells to radiation

Letrozole sensitizes breast cancer cells to ionizing radiation

HMGN1 loss sensitizes lung cancer cells to chemotherapy

ALDH1-mediated autophagy sensitizes glioblastoma cells to ferroptosis

ALDH1A inhibition sensitizes colon cancer cells to chemotherapy

A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

Survivin gene silencing sensitizes prostate cancer cells to selenium growth inhibition

miR-494 Sensitizes Gastric Cancer Cells to TRAIL Treatment Through Downregulation of Survivin

Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin

Albendazole sensitizes cancer cells to ionizing radiation

Hsp90 inhibition sensitizes DLBCL cells to cisplatin

Localization matters: nuclear-trapped Survivin sensitizes glioblastoma cells to temozolomide by elevating cellular senescence and impairing homologous recombination

FK228 sensitizes radioresistant small cell lung cancer cells to radiation

Letrozole sensitizes breast cancer cells to ionizing radiation

HMGN1 loss sensitizes lung cancer cells to chemotherapy

ALDH1-mediated autophagy sensitizes glioblastoma cells to ferroptosis

ALDH1A inhibition sensitizes colon cancer cells to chemotherapy

A cell-permeable dominant-negative survivin protein induces apoptosis and sensitizes prostate cancer cells to TNF-α therapy

Survivin gene silencing sensitizes prostate cancer cells to selenium growth inhibition

miR-494 Sensitizes Gastric Cancer Cells to TRAIL Treatment Through Downregulation of Survivin

Methylsulfonylmethane sensitizes endometrial cancer cells to doxorubicin

Albendazole sensitizes cancer cells to ionizing radiation

Hsp90 inhibition sensitizes DLBCL cells to cisplatin

Localization matters: nuclear-trapped Survivin sensitizes glioblastoma cells to temozolomide by elevating cellular senescence and impairing homologous recombination

FK228 sensitizes radioresistant small cell lung cancer cells to radiation

Letrozole sensitizes breast cancer cells to ionizing radiation

HMGN1 loss sensitizes lung cancer cells to chemotherapy

ALDH1-mediated autophagy sensitizes glioblastoma cells to ferroptosis

ALDH1A inhibition sensitizes colon cancer cells to chemotherapy

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