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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.17599852
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An epigenetic module common to the T lymphocyte.
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Pulmonary dendritic cells (CD11b(hi) CD14(hi) DC) are enriched for nestin.
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Rip kinase expression during early development in humans.
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NLR family genes influence homeobox transcription factor expression.
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Glucocorticoid resistance features changes in general transcription factor (GTF) expression.
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An expression screen to identify genes important for trastuzumab resistance: Ccl19.
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An expression screen to identify genes important for trastuzumab resistance: Meox2.
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An expression screen to identify genes important for trastuzumab resistance: Pax8-as1.
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Genes that function in axon guidance are associated with disease progression in breast and lung cancer.
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Therapeutic targeting in breast cancer for the treatment of lymph node metastasis: PIK3CD.
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Therapeutic targeting in HER2+ breast cancer to prevent and treat CNS disease: CD80.
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Clec2b and Clec11a, co-receptors for KIR2DL3 natural killer cell self discrimination complexes, are altered in expression in the cells of patients with IBD.
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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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Therapeutic targeting in breast cancer for the treatment of liver metastasis: TM4SF4.
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NLRC4 regulates a unique immunologic program.
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TSC22D4 gene activation in Crohn's Disease.
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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 lymph node metastasis: LILRA4.
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A comprehensive description of the circulating tumor cell: Fzd4/Fzd3.
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Therapeutic targeting in breast cancer for the treatment of lymph node metastasis: PTPN4.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of lung metastasis: GRIK4.
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Therapeutic targeting in HER2+ breast cancer to prevent and treat CNS disease: CDK4.
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Therapeutic targeting in HER2+ breast cancer to prevent and treat CNS disease: EFNA4.
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Therapeutic targeting in HER2+ breast cancer to prevent and treat CNS disease: EIF4G1.
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NLRP7 engagement in transformation and etiology of chronic disease.
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The range of Xist transcriptional targets in non-small cell lung cancer: BTBD7.
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Therapeutic targeting in HER2+ breast cancer to prevent and treat CNS disease: AIM1.
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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 breast cancer for the treatment of lymph node metastasis: MTF1.
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Xist is activated during resistance in triple negative breast cancer in vitro.
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Importin 8 is activated in childhood brain cancer.
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Therapeutic targeting in colorectal cancer for the treatment of the primary tumor: MAT1A.
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Telomerase control of Xist through Trf2.
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Phosphatase targeting in Luminal B breast cancer: PGP.
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Matrix metalloproteinases MMP1/MMP9 function in melanoma resistance.
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Phosphatase targeting in Luminal B breast cancer: PNKP.
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Therapeutic targeting in breast cancer for the treatment of metastasis to the skeletal system: SRC.
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ABC transporter multi-drug resistance genes ("pumps") in humans with non-small cell lung cancer.
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HSC, CMP and CLP in mice.
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