Regulation of vertebrate neural cell fate by transcription factors
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Using mouse genetics to study the developing spinal locomotor circuit
2020, The Neural Control of Movement: Model Systems and Tools to Study Locomotor FunctionFunctional determination of the differentiation potential of ventral mesencephalic neural precursor cells during dopaminergic neurogenesis
2017, Developmental BiologyCitation Excerpt :On the other hand, determination defines the stage at which cells differentiate according with their natural fate without the influence of the surrounding environment. Although NPC specification and commitment can be estimated by a code of gene expression (Bang and Goulding, 1996), a definitive evaluation can come only from a functional assay. Theoretically, a specified cell would continue its differentiation in the absence of external factors however, experimentally, this evaluation is limited by the survival of tissues or cells in the absence of growth factors.
Islet-1 is required for ventral neuron survival in Xenopus
2009, Biochemical and Biophysical Research CommunicationsThe amphibian second heart field: Xenopus islet-1 is required for cardiovascular development
2007, Developmental BiologyHaploinsufficiency of Runx1 results in the acceleration of mesodermal development and hemangioblast specification upon in vitro differentiation of ES cells
2004, BloodCitation Excerpt :The expression of Rex1, a zinc finger transcription factor found in ES cells but not in their differentiated progeny,11 was rapidly shut down upon differentiation of the 3 ES cell lines, consistent with the rapid loss of potential to generate secondary EBs (Figure 1E). NeuroD,12 a gene expressed in ES cells but down-regulated upon differentiation in conditions that do not support neuronal development, was also rapidly down-regulated in the EBs generated from the 3 different ES cell lines. Fgf5, a gene expressed in the epiblast of the early embryo,13 displayed a similar pattern in EBs from all 3 cell lines.