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Main Author:	Mamoor, Shahan
Format:	Recurso digital
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Published:	Zenodo 2025
Online Access:	https://doi.org/10.5281/zenodo.14602347
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The range of Xist transcriptional targets in non-small cell lung cancer: BTBD7.
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Xist is activated during resistance in triple negative breast cancer in vitro.
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ATM defects result in Xist modulation.
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ABC transporter multi-drug resistance genes ("pumps") in humans with non-small cell lung cancer.
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Telomerase control of Xist through Trf2.
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The genes encoded at the Dxz locus, DANT2/3, are components of an Xist gene expression regulation apparatus that utilizes quantitative control of message quantity of specific genes to measure and maintain transcription, globally, within homeostatic range.
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Deletion of repeat B and C of Xist results in induction of SATB1.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: ENOPH1.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: MTFP1.
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BAALC: Therapeutic targeting in lung cancer for the treatment of lymph node metastasis.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: CDK7.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: WNK3.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: PANK1.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: FJX1.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: RPL19.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: PFKFB4.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: SHMT2.
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Therapeutic targeting in lung cancer for the treatment of lymph node metastasis: CAMTA1.
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Therapeutic targeting in lung cancer for the treatment of lymph node metastasis: GRIK3.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of lung metastasis: EREG.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of lung metastasis: CTNNBL1.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: PPP6R1.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of lung metastasis: GRIK4.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of lung metastasis: ATAD1.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of lung metastasis: GPR158.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: PPP1R9A.
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Therapeutic targeting in breast cancer for the treatment of lung metastasis: PPP1R9A.
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Phosphatase targeting in Luminal B breast cancer: PGP.
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Phosphatase targeting in Luminal B breast cancer: PNKP.
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Kinase targeting in Luminal B breast cancer: DTYMK.
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Genes that function in axon guidance are associated with disease progression in breast and lung cancer.
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The integral membrane protein SMIM38 is transcriptionally activated in circulating tumor cells in human breast cancer in conjunction with two SMIM38-interacting proteins of undefined function, ETDA and ETDB.
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Therapeutic targeting in colorectal cancer for the treatment of the primary tumor: TGFBI.
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Therapeutic targeting in breast cancer for the treatment of liver metastasis: AFM.
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Therapeutic targeting in colorectal cancer for the treatment of liver metastasis: MAF.
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Therapeutic targeting in breast cancer for the treatment of liver metastasis: HHEX.
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Therapeutic targeting in breast cancer for the treatment of liver metastasis: BAAT.
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Kinase targeting in Luminal B breast cancer: CDK5.
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The homeobox transcription factor TCF7 is activated in and likely required for metastasis to the lymph nodes in humans with breast cancer.
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The homeobox transcription factor MEOX1 is activated in and likely required for metastasis to the lymph nodes in humans with breast cancer.
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Published: (2025)