Search results for "cell fate"

showing 5 items of 75 documents

Cell lineage and cell fate specification in the embryonic CNS of Drosophila.

1997

The Drosophila CNS derives from a population of neural stem cells, called neuroblasts (NBs), which delaminate individually from the neurogenic region of the ectoderm. In the embryonic ventral nerve cord each NB can be uniquely identified and gives rise to a specific lineage consisting of neurons and/or glial cells. This 'NB identity' is dependent on the position of the progenitor cells in the neuroectoderm before delamination. The positional information is provided by the products of segment polarity and dorsoventral (D/V) patterning genes. Subsequently, 'cell fate genes' like huckebein (hkb) and eagle (eg) contribute to the generation of specific NB lineages. These genes act downstream of …

education.field_of_studyNeuroectodermPopulationEctodermCell BiologyAnatomyBiologyCell fate determinationEmbryonic stem cellNeural stem cellCell biologymedicine.anatomical_structureNeuroblastmedicineProgenitor celleducationDevelopmental BiologySeminars in celldevelopmental biology
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Molecular Basis for the Regulation of Cell Fate by the Lethal (2) Giant Larvae Tumour Suppressor Gene of Drosophila Melanogaster

2007

Tumour suppressor genes act as recessive determinants of cancer. Their function is required for normal cell growth and differentiation during development. When both alleles of these developmental genes are inactivated, cell growth becomes unrestricted. In Drosophila, a series of genes have been identified which when mutated produce tissue-specific tumours. Of these the lethal(2)giant larvae (l(2)gl) gene is the best studied. Homozygous l(2)gl mutations cause the development of malignant tumours in the brain and the imaginal discs. Genomic DNA from the l(2)gl locus has been cloned, introduced back into l(2)gl mutant animals by P-element-mediated transformation and shown to restore normal dev…

genomic DNAbiologyMutantmedicineEmbryoLocus (genetics)Drosophila melanogasterCell fate determinationCarcinogenesismedicine.disease_causebiology.organism_classificationMolecular biologyGene
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Author response: Notch and TLR signaling coordinate monocyte cell fate and inflammation

2020

medicine.anatomical_structureMonocytemedicineInflammationmedicine.symptomBiologyCell fate determinationCell biology
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Intravenous SPION-labeled adipocyte-derived stem cells targeted to the brain by magnetic attraction in a rat stroke model: An ultrastructural insight…

2021

Abstract Mesenchymal stem cell therapy after stroke is a promising option investigated in animal models and clinical trials. The intravenous route is commonly used in clinical settings guaranteeing an adequate safety profile although low yields of engraftment. In this report, rats subjected to ischemic stroke were injected with adipose-derived stem cells (ADSCs) labeled with superparamagnetic iron oxide nanoparticles (SPIONs) applying an external magnetic field in the skull to retain the cells. Although most published studies demonstrate viability of ADSCs, only a few have used ultrastructural techniques. In our study, the application of a local magnetic force resulted in a tendency for hig…

medicine.medical_treatmentBiomedical EngineeringPharmaceutical ScienceMedicine (miscellaneous)BioengineeringCell fate determinationCorrelative microscopy Electron microscopy Magnetic fields SPION Stem cell therapy Strokechemistry.chemical_compoundAdipocyteAdipocytesmedicineAnimalsGeneral Materials ScienceMagnetite NanoparticlesStrokeMicrogliaStem CellsMesenchymal stem cellBrainStem-cell therapymedicine.diseaseMagnetic Resonance ImagingRatsCell biologyStrokeMagnetic Fieldsmedicine.anatomical_structurechemistryUltrastructureMolecular MedicineStem cellNanomedicine: Nanotechnology, Biology and Medicine
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Digital control circuitry for the p53 dynamics in cancer cell and apoptosis

2010

Abstract Experimental work and theoretical models deduce a “digital” response of the p53 transcription factor when genomic integrity is damaged. The mutual influence of p53 and its antagonist, the Mdm2 oncogene, is closed in a feedback. This paper proposes an aerospace-based architecture for translating the p53/Mdm2/DNA damage network into a digital circuitry in which the optimal control theory is applied for obtaining the requested dynamic evolutions of some considered cell species for repairing a DNA damage. The purpose of this paper is to demonstrate the usefulness of such digital circuitry design to detect and predict the cell species dynamics for shedding light on their inner and mutua…

p53General Immunology and MicrobiologyMechanism (biology)DNA damageQH301-705.5General NeuroscienceapoptosisWiring diagramCell fate determinationBiologycellular circuitryBioinformaticsOptimal controlGeneral Biochemistry Genetics and Molecular Biologyprotein networks signallingfeedback controlCancer cellDigital controlBiology (General)General Agricultural and Biological SciencesBiological systemTranscription factorOpen Life Sciences
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