Christopher A. Walsh, MD, PhD(26)

Journal of Biological Chemistry. 2000 275: 34442-34450.

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Autosomal recessive lissencephaly with cerebellar hypoplasia (LCH) is associated with human reelin gene mutations

Hong SE, Huang DT, Shugart YY, Al Shahwan S, Grant PE, Hourihane JOB, Martin NDT, Walsh CA.
Nature Genetics. 2000 26: 93-96.
Article

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Reelin binds a3&Mac254;1 integrin and inhibits neuronal migration

Dulabon L, Olson EC, Gordy M, Eisenhuth S, McGrath B, Walsh CA, Kreidberg JA, Anton ES.
Neuron. 2000 27: 33-44
Article

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DCAMKL1 encodes a protein kinase with homology to Doublecortin that regulates microtubule polymerization in a kinase-independent fashion

Lin PT, Glesson JG, Corbo JC, Flanagan L, Walsh CA
J. Neurosci. 2000 20: 9152-9161
Article

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Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation (责任编辑：泉水)

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Christopher A. Walsh, MD, PhD(26)