Local therapeutic platform prevents postsurgical GBM recurrence by diminishing GICs and reshaping immunosuppressive microenvironment. [PDF]
Zhu M +10 more
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Roxadustat: A catalyst for diabetic wound healing through re-epithelialization and angiogenesis. [PDF]
Tang D, Lin Q, Xu K, Lu QP.
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Reply to: "<i>NOTCH1</i>: A Potential New Biomarker in the Era of Immunotherapy?" and "Caution in Interpreting <i>NOTCH1</i> Mutation as a Predictive Biomarker of Tislelizumab Response in Esophageal Squamous Cell Carcinoma". [PDF]
Lu Z +5 more
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Hif-1 responsive IFFLs to explain specific transcriptional responses to cycling hypoxia in cancers. [PDF]
Qiu X +5 more
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Caution in Interpreting <i>NOTCH1</i> Mutation as a Predictive Biomarker of Tislelizumab Response in Esophageal Squamous Cell Carcinoma. [PDF]
Lu Z +6 more
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<i>NOTCH1</i>: A Potential New Biomarker in the Era of Immunotherapy? [PDF]
Aydemir E, Öksüz NE, Bir Yücel K.
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Targeting the Notch signaling pathway: molecular mechanisms and therapeutic strategies for cardiac repair after myocardial infarction. [PDF]
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Related searches:
Targeting NOTCH1 in Hematopoietic Malignancy
Critical Reviews™ in Oncogenesis, 2011NOTCH1 is a well-validated target in hematopoietic malignancy, with NOTCH1 activating mutations identified in more than 50% of T-cell acute lymphoblastic leukemias. Moreover, a recent report has identified NOTCH1 activating mutations in 12% of chronic lymphocytic leukemias.
ROTI, GIOVANNI, Stegmaier K.
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Cancer Mutations that activate Notch have been identified in several cancers. Weiland et al. find that Notch1 signaling within endothelial cells (ECs) promotes the invasion of distant organs by tumors. Abnormally high levels of active Notch1 are found in blood vessels associated with advanced human cancers.
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p53 regulates thymic Notch1 activation
European Journal of Immunology, 2004AbstractNotch is crucial for multiple stages of T cell development, including the CD4+CD8+ double positive (DP)/CD8+ single positive (SP) transition, but regulation of Notchactivation is not well understood. p53 regulates Presenilin1 (PS1) expression, and PS1 cleaves Notch, releasing its intracellular domain (NIC), leading to the expression of ...
Amy M, Laws, Barbara A, Osborne
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