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1999 1
2000 4
2020 0
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Page 1
Potential mechanisms of mutations that affect neuronal migration in man and mouse.
Walsh CA, Goffinet AM. Walsh CA, et al. Curr Opin Genet Dev. 2000 Jun;10(3):270-4. doi: 10.1016/s0959-437x(00)00076-9. Curr Opin Genet Dev. 2000. PMID: 10826984 Review.
Genetic malformations of the human cerebral cortex.
Walsh CA. Walsh CA. Neuron. 1999 May;23(1):19-29. doi: 10.1016/s0896-6273(00)80749-7. Neuron. 1999. PMID: 10402190 Free article. Review. No abstract available.
Reelin binds alpha3beta1 integrin and inhibits neuronal migration.
Dulabon L, Olson EC, Taglienti MG, Eisenhuth S, McGrath B, Walsh CA, Kreidberg JA, Anton ES. Dulabon L, et al. Neuron. 2000 Jul;27(1):33-44. doi: 10.1016/s0896-6273(00)00007-6. Neuron. 2000. PMID: 10939329 Free article.
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA. Hong SE, et al. Nat Genet. 2000 Sep;26(1):93-6. doi: 10.1038/79246. Nat Genet. 2000. PMID: 10973257
DCAMKL1 encodes a protein kinase with homology to doublecortin that regulates microtubule polymerization.
Lin PT, Gleeson JG, Corbo JC, Flanagan L, Walsh CA. Lin PT, et al. J Neurosci. 2000 Dec 15;20(24):9152-61. doi: 10.1523/JNEUROSCI.20-24-09152.2000. J Neurosci. 2000. PMID: 11124993 Free PMC article.
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