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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.15182129
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Gasdermin activation during lineage specification in the human embryo.
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Androgen signaling has functions in lineage commitment in the human embryo.
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The mIR-302 cluster is silenced upon differentiation to the mechanosensory lineage.
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Casz1 mobilization during TE lineage specification from the pluripotent state in embryonic stem cells.
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A retrotransposon-like gene, RTL5, is modulated during differentiation of embryonic stem cells to the trophectoderm lineage.
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Haglr, a HOXD antisense growth-associated long non-coding RNA with functions in lineage commitment in the human embryo.
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Control of TOX transcription factors by the Hippo signaling pathway.
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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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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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Kinase activation during small molecule inhibition of the receptors for the vascular endothelial growth factors VEGFR1 and VEGFR2.
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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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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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Therapeutic targeting in breast cancer for the treatment of metastasis to the skeletal system: SRC.
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Published: (2025)

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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Therapeutic targeting in breast cancer for the treatment of lymph node metastasis: MYO9B.
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Therapeutic targeting in breast cancer for the treatment of lymph node metastasis: NFATC1.
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Aire is a component gene of the Th17 gene signature.
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Therapeutic targeting in breast cancer for the treatment of lymph node metastasis: GDF5.
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Therapeutic targeting in breast cancer for the treatment of metastasis to the skeletal system: INPP5F.
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A comprehensive description of the circulating tumor cell: TM6SF1.
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FCGRT functions in senescence and transformation.
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Immunoglobulin-based therapeutic targeting in breast cancer for the treatment of liver metastasis: ACSM2B.
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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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Leukotriene activation in the blood of humans with high CRP.
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TSC22D4 gene activation in Crohn's Disease.
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