1. Kim MH, Cierpicki T, Derewenda U, Krowarsch D, Feng Y, Devedjiev Y, Dauter Z, Walsh CA, Otlewski J, Bushweller JH et al.. (2003) The DCX-domain tandems of doublecortin and doublecortin-like kinase.. Nat Struct Biol, 10 (5): (324-33). [PMID:12692530] |
2. des Portes, V V and 13 more authors.. (1998) A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.. Cell, (9): [PMID:9489699] |
3. Gleeson, J G JG and 10 more authors.. (1998) Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.. Cell, (9): [PMID:9489700] |
4. des Portes, V V and 15 more authors.. (1998) doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH).. Human molecular genetics, [PMID:9618162] |
5. Sossey-Alaoui, K K and 8 more authors.. (1998) Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.. Human molecular genetics, [PMID:9668176] |
6. Pilz, D T DT and 10 more authors.. (1998) LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.. Human molecular genetics, [PMID:9817918] |
7. Gleeson, J G JG and 24 more authors.. (1999) Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.. Annals of neurology, [PMID:9989615] |
8. Kato, M M and 7 more authors.. (1999) A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia.. Human genetics, [PMID:10369164] |
9. Pilz, D T DT and 7 more authors.. (1999) Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.. Human molecular genetics, [PMID:10441340] |
10. Sakamoto, M M, Ono, J J, Okada, S S, Nakamura, Y Y and Kurahashi, H H.. (2000) Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.. Journal of human genetics, [PMID:10807542] |
11. Matsumoto, N N and 11 more authors.. (2001) Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.. European journal of human genetics : EJHG, [PMID:11175293] |
12. Demelas, L L and 10 more authors.. (2001) Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.. Neurology, (24): [PMID:11468322] |
13. Kato, M M and 8 more authors.. (2001) Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.. Annals of neurology, [PMID:11601509] |
14. des Portes, V V and 8 more authors.. (2002) So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation.. Seizure, [PMID:12027577] |
15. D'Agostino, Maria Daniela MD and 31 more authors.. (2002) Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.. Brain : a journal of neurology, [PMID:12390976] |
16. Aigner, L L and 14 more authors.. (2003) Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders.. Neurology, (28): [PMID:12552055] |
17. Ross, Mark T MT and 281 more authors.. (2005) The DNA sequence of the human X chromosome.. Nature, (17): [PMID:15772651] |
18. Slepak, Tatiana I; Salay, Lindsey D; Lemmon, Vance P and Bixby, John L.. (2012) Dyrk kinases regulate phosphorylation of doublecortin, cytoskeletal organization, and neuronal morphology.. Cytoskeleton (Hoboken, N.J.), [PMID:22359282] |
19. Homan, Claire C CC and 10 more authors.. (2014) Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.. American journal of human genetics, (6): [PMID:24607389] |
20. Tsai, Meng-Han MH and 9 more authors.. (2016) A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, [PMID:27292316] |