Buckler A - Search Results

1

Frequency of homozygous deletion at p16/CDKN2 in primary human tumours.

Cairns P, Polascik TJ, Eby Y, Tokino K, Califano J, Merlo A, Mao L, Herath J, Jenkins R, Westra W, Rutter JL, Buckler A, Gabrielson E, Tockman M, Cho KR, Hedrick L, Bova GS, Isaacs W, Koch W, Schwab D, Sidransky D, et al. Cairns P, et al. Among authors: buckler a. Nat Genet. 1995 Oct;11(2):210-2. doi: 10.1038/ng1095-210. Nat Genet. 1995. PMID: 7550353

2

MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p.

Ueki K, Rubio MP, Ramesh V, Correa KM, Rutter JL, von Deimling A, Buckler AJ, Gusella JF, Louis DN. Ueki K, et al. Among authors: buckler aj. Hum Mol Genet. 1994 Oct;3(10):1841-5. doi: 10.1093/hmg/3.10.1841. Hum Mol Genet. 1994. PMID: 7849711

3

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.

Church DM, Stotler CJ, Rutter JL, Murrell JR, Trofatter JA, Buckler AJ. Church DM, et al. Among authors: buckler aj. Nat Genet. 1994 Jan;6(1):98-105. doi: 10.1038/ng0194-98. Nat Genet. 1994. PMID: 8136842

4

Mutational analysis of CDKN2 (MTS1/p16ink4) in human breast carcinomas.

Xu L, Sgroi D, Sterner CJ, Beauchamp RL, Pinney DM, Keel S, Ueki K, Rutter JL, Buckler AJ, Louis DN, et al. Xu L, et al. Among authors: buckler aj. Cancer Res. 1994 Oct 15;54(20):5262-4. Cancer Res. 1994. PMID: 7923151

5

A 500-kilobase region containing the tuberous sclerosis locus (TSC1) in a 1.7-megabase YAC and cosmid contig.

Murrell J, Trofatter J, Rutter M, Cutone S, Stotler C, Rutter J, Long K, Turner A, Deaven L, Buckler A, et al. Murrell J, et al. Among authors: buckler a. Genomics. 1995 Jan 1;25(1):59-65. doi: 10.1016/0888-7543(95)80109-y. Genomics. 1995. PMID: 7774956

6

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.

Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO. Ozelius LJ, et al. Among authors: buckler aj. Nat Genet. 1997 Sep;17(1):40-8. doi: 10.1038/ng0997-40. Nat Genet. 1997. PMID: 9288096

7

Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma.

Ingraham SE, Lynch RA, Surti U, Rutter JL, Buckler AJ, Khan SA, Menon AG, Lepont P. Ingraham SE, et al. Among authors: buckler aj. Mutat Res. 2006 Dec 1;602(1-2):43-53. doi: 10.1016/j.mrfmmm.2006.07.007. Epub 2006 Oct 12. Mutat Res. 2006. PMID: 17045619

8

p16 alterations and deletion mapping of 9p21-p22 in malignant mesothelioma.

Cheng JQ, Jhanwar SC, Klein WM, Bell DW, Lee WC, Altomare DA, Nobori T, Olopade OI, Buckler AJ, Testa JR. Cheng JQ, et al. Among authors: buckler aj. Cancer Res. 1994 Nov 1;54(21):5547-51. Cancer Res. 1994. PMID: 7923195

9

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.

Harley HG, Brook JD, Rundle SA, Crow S, Reardon W, Buckler AJ, Harper PS, Housman DE, Shaw DJ. Harley HG, et al. Among authors: buckler aj. Nature. 1992 Feb 6;355(6360):545-6. doi: 10.1038/355545a0. Nature. 1992. PMID: 1346923

10

Cloning of the alpha-adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification.

Taylor SA, Snell RG, Buckler A, Ambrose C, Duyao M, Church D, Lin CS, Altherr M, Bates GP, Groot N, et al. Taylor SA, et al. Among authors: buckler a. Nat Genet. 1992 Nov;2(3):223-7. doi: 10.1038/ng1192-223. Nat Genet. 1992. PMID: 1345173

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