DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson’s disease-Reference-Cited by-同舟云学术

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DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson’s disease

Published:2014-06 Issue:6 Volume:5 Page:e1289-e1289
ISSN:2041-4889
Container-title:Cell Death & Disease
language:en
Short-container-title:Cell Death Dis

Author:

Barallobre M J,Perier C,Bové J,Laguna A,Delabar J M,Vila M,Arbonés M L

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology,Cellular and Molecular Neuroscience,Immunology

Link

http://www.nature.com/articles/cddis2014253.pdf

Reference49 articles.

1. Guedj F, Pereira PL, Najas S, Barallobre MJ, Chabert C, Souchet B et al. DYRK1A: a master regulatory protein controlling brain growth. Neurobiol Dis 2012; 46: 190–203.

2. Moller RS, Kubart S, Hoeltzenbein M, Heye B, Vogel I, Hansen CP et al. Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly. Am J Hum Genet 2008; 82: 1165–1170.

3. van Bon BW, Hoischen A, Hehir-Kwa J, de Brouwer AP, Ruivenkamp C, Gijsbers AC et al. Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly. Clin Genet 2011; 79: 296–299.

4. Yamamoto T, Shimojima K, Nishizawa T, Matsuo M, Ito M, Imai K . Clinical manifestations of the deletion of Down syndrome critical region including DYRK1A and KCNJ6. Am J Med Genet A 2011; 155A: 113–119.

5. Courcet JB, Faivre L, Malzac P, Masurel-Paulet A, Lopez E, Callier P et al. The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy. J Med Genet 2012; 49: 731–736.

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