pubmed-article:21569278 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C0025462 | lld:lifeskim |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C0521390 | lld:lifeskim |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C0037083 | lld:lifeskim |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C0282151 | lld:lifeskim |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C1414395 | lld:lifeskim |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
pubmed-article:21569278 | lifeskim:mentions | umls-concept:C1527148 | lld:lifeskim |
pubmed-article:21569278 | pubmed:dateCreated | 2011-6-1 | lld:pubmed |
pubmed-article:21569278 | pubmed:abstractText | Dopaminergic neurons of the ventral mesodiencephalon are affected in significant health disorders such as Parkinson's disease, schizophrenia, and addiction. The ultimate goal of current research endeavors is to improve the clinical treatment of such disorders, such as providing a protocol for cell replacement therapy in Parkinson's disease that will successfully promote the specific differentiation of a stem cell into a dopaminergic neuronal phenotype. Decades of research on the developmental mechanisms of the mesodiencephalic dopaminergic (mdDA) system have led to the identification of many signaling pathways and transcription factors critical in its development. The unraveling of these pathways will help fill in the pieces of the puzzle that today dominates neurodevelopment research: how to make and maintain a mdDA neuron. In the present review, we provide an overview of the mdDA system, the processes and signaling molecules involved in its genesis, with a focus on the transcription factor En1 and the canonical Wnt pathway, highlighting recent findings on their relevance--and interplay--in the development and maintenance of the mdDA system. | lld:pubmed |
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