001     137288
005     20240321220225.0
024 7 _ |a 10.1093/jmcb/mjt046
|2 doi
024 7 _ |a pmid:24326514
|2 pmid
024 7 _ |a 1673-520X
|2 ISSN
024 7 _ |a 1674-2788
|2 ISSN
024 7 _ |a 1759-4685
|2 ISSN
037 _ _ |a DZNE-2020-03610
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Wurst, Wolfgang
|0 P:(DE-2719)2000028
|b 0
|e First author
245 _ _ |a Wnt1-regulated genetic networks in midbrain dopaminergic neuron development.
260 _ _ |a Oxford
|c 2014
|b Oxford Univ. Press
264 _ 1 |3 online
|2 Crossref
|b Oxford University Press (OUP)
|c 2013-12-09
264 _ 1 |3 print
|2 Crossref
|b Oxford University Press (OUP)
|c 2014-02-01
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1591163871_16757
|2 PUB:(DE-HGF)
|x Review Article
336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Neurons synthesizing the neurotransmitter dopamine exert crucial functions in the mammalian brain. The biggest and most important population of dopamine-synthesizing neurons is located in the mammalian ventral midbrain (VM), and controls and modulates the execution of motor, cognitive, affective, motivational, and rewarding behaviours. Degeneration of these neurons leads to motor deficits that are characteristic of Parkinson's disease, while their dysfunction is involved in the pathogenesis of psychiatric disorders including schizophrenia and addiction. Because the aetiology and therapeutic prospects for these diseases include neurodevelopmental aspects, substantial scientific interest has been focused on deciphering the mechanistic pathways that control the generation and survival of these neurons during embryonic development. Researches during the last decade revealed the pivotal role of the secreted Wnt1 ligand and its signalling cascade in the generation of the dopamine-synthesizing neurons in the mammalian VM. Here, we summarize the initial and more recent findings that have unravelled several Wnt1-controlled genetic networks required for the proliferation and commitment of VM progenitors to the dopaminergic cell fate during midgestational embryonic stages, and for the correct differentiation of these progenitors into postmitotic dopamine-synthesizing neurons at late midgestational embryonic and foetal stages.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
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588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Wnt1 Protein
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Dopaminergic Neurons: cytology
|2 MeSH
650 _ 2 |a Dopaminergic Neurons: metabolism
|2 MeSH
650 _ 2 |a Dopaminergic Neurons: physiology
|2 MeSH
650 _ 2 |a Gene Regulatory Networks
|2 MeSH
650 _ 2 |a Mesencephalon: cytology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Models, Biological
|2 MeSH
650 _ 2 |a Wnt Signaling Pathway: physiology
|2 MeSH
650 _ 2 |a Wnt1 Protein: genetics
|2 MeSH
650 _ 2 |a Wnt1 Protein: metabolism
|2 MeSH
650 _ 2 |a Wnt1 Protein: physiology
|2 MeSH
700 1 _ |a Prakash, Nilima
|0 P:(DE-2719)9000256
|b 1
|e Last author
773 1 8 |a 10.1093/jmcb/mjt046
|b : Oxford University Press (OUP), 2013-12-09
|n 1
|p 34-41
|3 journal-article
|2 Crossref
|t Journal of Molecular Cell Biology
|v 6
|y 2013
|x 1674-2788
773 _ _ |a 10.1093/jmcb/mjt046
|g Vol. 6, no. 1, p. 34 - 41
|0 PERI:(DE-600)2500949-7
|n 1
|q 6:1<34 - 41
|p 34-41
|t Journal of molecular cell biology
|v 6
|y 2013
|x 1674-2788
909 C O |p VDB
|o oai:pub.dzne.de:137288
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 0
|6 P:(DE-2719)2000028
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 1
|6 P:(DE-2719)9000256
913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
|l Erkrankungen des Nervensystems
|1 G:(DE-HGF)POF3-340
|0 G:(DE-HGF)POF3-342
|2 G:(DE-HGF)POF3-300
|v Disease Mechanisms and Model Systems
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914 1 _ |y 2014
915 _ _ |a Nationallizenz
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21