Allen KM - Search Results

1

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motté J, Mira AP, Scheffer I, Berkovic S, Scaravilli F, King RA, Ledbetter DH, Schlessinger D, Dobyns WB, Walsh CA. Ross ME, et al. Among authors: allen km. Hum Mol Genet. 1997 Apr;6(4):555-62. doi: 10.1093/hmg/6.4.555. Hum Mol Genet. 1997. PMID: 9097958

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: allen km. Cell. 1998 Jan 9;92(1):63-72. doi: 10.1016/s0092-8674(00)80899-5. Cell. 1998. PMID: 9489700 Free article.

3

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: allen km. Hum Mol Genet. 1998 Dec;7(13):2029-37. doi: 10.1093/hmg/7.13.2029. Hum Mol Genet. 1998. PMID: 9817918

4

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.

Gleeson JG, Minnerath SR, Fox JW, Allen KM, Luo RF, Hong SE, Berg MJ, Kuzniecky R, Reitnauer PJ, Borgatti R, Mira AP, Guerrini R, Holmes GL, Rooney CM, Berkovic S, Scheffer I, Cooper EC, Ricci S, Cusmai R, Crawford TO, Leroy R, Andermann E, Wheless JW, Dobyns WB, Walsh CA, et al. Gleeson JG, et al. Among authors: allen km. Ann Neurol. 1999 Feb;45(2):146-53. doi: 10.1002/1531-8249(199902)45:2<146::aid-ana3>3.0.co;2-n. Ann Neurol. 1999. PMID: 9989615

5

Genes that regulate neuronal migration in the cerebral cortex.

Allen KM, Walsh CA. Allen KM, et al. Epilepsy Res. 1999 Sep;36(2-3):143-54. doi: 10.1016/s0920-1211(99)00048-0. Epilepsy Res. 1999. PMID: 10515162 Review.

6

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. Genomics. 1998 Sep 1;52(2):214-8. doi: 10.1006/geno.1998.5424. Genomics. 1998. PMID: 9782089

7

Studies of the candidate genes in X-linked congenital cerebellar hypoplasia.

Illarioshkin SN, Allen KM, Gleeson JG, Tsuji S, Ikeuchi T, Markova ED, Walsh CA, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. Among authors: allen km. J Neurol. 1999 Dec;246(12):1177-80. doi: 10.1007/s004150050539. J Neurol. 1999. PMID: 10653312

8

Shaking down new epilepsy genes.

Allen KM, Walsh C. Allen KM, et al. Nat Med. 1996 May;2(5):516-8. doi: 10.1038/nm0596-516. Nat Med. 1996. PMID: 8616704 Review. No abstract available.

9

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. Nat Genet. 1998 Sep;20(1):25-30. doi: 10.1038/1675. Nat Genet. 1998. PMID: 9731525

10

Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

Bienvenu T, des Portes V, McDonell N, Carrié A, Zemni R, Couvert P, Ropers HH, Moraine C, van Bokhoven H, Fryns JP, Allen K, Walsh CA, Boué J, Kahn A, Chelly J, Beldjord C. Bienvenu T, et al. Am J Med Genet. 2000 Aug 14;93(4):294-8. doi: 10.1002/1096-8628(20000814)93:4<294::aid-ajmg8>3.0.co;2-f. Am J Med Genet. 2000. PMID: 10946356

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