Walsh CA - Search Results

1

Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival.

Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Muna Al-Saffar, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, Zaki MS, Sultan T, Burglen L, Rajab A, Al-Gazali L, Mochida GH, Harris MP, Gleeson JG, Walsh CA. Coulter ME, et al. Among authors: walsh ca. Genet Med. 2020 Jun;22(6):1040-1050. doi: 10.1038/s41436-020-0758-9. Epub 2020 Feb 27. Genet Med. 2020. PMID: 32103185 Free PMC article.

2

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.

Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Cell. 1998 Jan 9;92(1):63-72. doi: 10.1016/s0092-8674(00)80899-5. Cell. 1998. PMID: 9489700 Free article.

3

PAK3 mutation in nonsyndromic X-linked mental retardation.

Allen KM, Gleeson JG, Bagrodia S, Partington MW, MacMillan JC, Cerione RA, Mulley JC, Walsh CA. Allen KM, et al. Among authors: walsh ca. Nat Genet. 1998 Sep;20(1):25-30. doi: 10.1038/1675. Nat Genet. 1998. PMID: 9731525

4

A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3.

Allen KM, Gleeson JG, Shoup SM, Walsh CA. Allen KM, et al. Among authors: walsh ca. Genomics. 1998 Sep 1;52(2):214-8. doi: 10.1006/geno.1998.5424. Genomics. 1998. PMID: 9782089

5

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME. Pilz DT, et al. Among authors: walsh ca. Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029. Hum Mol Genet. 1998. PMID: 9817918

6

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons.

Gleeson JG, Lin PT, Flanagan LA, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Neuron. 1999 Jun;23(2):257-71. doi: 10.1016/s0896-6273(00)80778-3. Neuron. 1999. PMID: 10399933 Free article.

7

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly.

Dobyns WB, Truwit CL, Ross ME, Matsumoto N, Pilz DT, Ledbetter DH, Gleeson JG, Walsh CA, Barkovich AJ. Dobyns WB, et al. Among authors: walsh ca. Neurology. 1999 Jul 22;53(2):270-7. doi: 10.1212/wnl.53.2.270. Neurology. 1999. PMID: 10430413

8

Genetic and neuroradiological heterogeneity of double cortex syndrome.

Gleeson JG, Luo RF, Grant PE, Guerrini R, Huttenlocher PR, Berg MJ, Ricci S, Cusmai R, Wheless JW, Berkovic S, Scheffer I, Dobyns WB, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Ann Neurol. 2000 Feb;47(2):265-9. Ann Neurol. 2000. PMID: 10665503

9

Neuronal migration disorders: from genetic diseases to developmental mechanisms.

Gleeson JG, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Trends Neurosci. 2000 Aug;23(8):352-9. doi: 10.1016/s0166-2236(00)01607-6. Trends Neurosci. 2000. PMID: 10906798 Review.

10

Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes.

Gleeson JG, Minnerath S, Kuzniecky RI, Dobyns WB, Young ID, Ross ME, Walsh CA. Gleeson JG, et al. Among authors: walsh ca. Am J Hum Genet. 2000 Sep;67(3):574-81. doi: 10.1086/303043. Epub 2000 Jul 27. Am J Hum Genet. 2000. PMID: 10915612 Free PMC article.

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