The evolving doublecortin (DCX) superfamily-Reference-Cited by-同舟云学术

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The evolving doublecortin (DCX) superfamily

Published:2006-07-26 Issue:1 Volume:7 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

Reiner Orly,Coquelle Frédéric M,Peter Bastian,Levy Talia,Kaplan Anna,Sapir Tamar,Orr Irit,Barkai Naama,Eichele Gregor,Bergmann Sven

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

http://link.springer.com/content/pdf/10.1186/1471-2164-7-188.pdf

Reference51 articles.

1. des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrie A, Gelot A, Dupuis E, Motte J, Berwald-Netter Y, Catala M, Kahn A, Beldjord C, Chelly J: A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar hetrotropia and lissencephaly syndrome. Cell. 1998, 92: 51-61. 10.1016/S0092-8674(00)80898-3.

2. Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA: doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell. 1998, 92: 63-72. 10.1016/S0092-8674(00)80899-5.

3. Reiner O, Coquelle FM: Missense mutations resulting in type 1 lissencephaly. Cell Mol Life Sci. 2005, 62 (4): 425-434. 10.1007/s00018-004-4344-0.

4. Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH: Lissencephaly: a human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. J Am med Ass. 1993, 270: 2838-2842. 10.1001/jama.270.23.2838.

5. Barkovich AJ, Guerrini R, Battaglia G, Kalifa G, N'Guyen T, Parmeggiani A, Santucci M, Giovanardi-Rossi P, Granata T, D'Incerti L: Band heterotopia: correlation of outcome with magnetic resonance imaging parameters. Ann Neurol. 1994, 36 (4): 609-617. 10.1002/ana.410360409.

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