McWilliam P - Search Results

1

Gene expression differences between the microsatellite instability (MIN) and chromosomal instability (CIN) phenotypes in colorectal cancer revealed by high-density cDNA array hybridization.

Dunican DS, McWilliam P, Tighe O, Parle-McDermott A, Croke DT. Dunican DS, et al. Among authors: mcwilliam p. Oncogene. 2002 May 9;21(20):3253-7. doi: 10.1038/sj.onc.1205431. Oncogene. 2002. PMID: 12082642

2

The leukocyte protein L-plastin induces proliferation, invasion and loss of E-cadherin expression in colon cancer cells.

Foran E, McWilliam P, Kelleher D, Croke DT, Long A. Foran E, et al. Among authors: mcwilliam p. Int J Cancer. 2006 Apr 15;118(8):2098-104. doi: 10.1002/ijc.21593. Int J Cancer. 2006. PMID: 16287074 Free article.

3

Serial analysis of gene expression identifies putative metastasis-associated transcripts in colon tumour cell lines.

Parle-McDermott A, McWilliam P, Tighe O, Dunican D, Croke DT. Parle-McDermott A, et al. Among authors: mcwilliam p. Br J Cancer. 2000 Sep;83(6):725-8. doi: 10.1054/bjoc.2000.1330. Br J Cancer. 2000. PMID: 10952775 Free PMC article.

4

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity.

Farrar GJ, McWilliam P, Bradley DG, Kenna P, Lawler M, Sharp EM, Humphries MM, Eiberg H, Conneally PM, Trofatter JA, et al. Farrar GJ, et al. Among authors: mcwilliam p. Genomics. 1990 Sep;8(1):35-40. doi: 10.1016/0888-7543(90)90223-h. Genomics. 1990. PMID: 2081598

5

Frequency of deletion 508 among Irish cystic fibrosis patients.

De Arce MA, Mulherin D, McWilliam P, Lawler M, FitzGerald MX, Humphries P. De Arce MA, et al. Among authors: mcwilliam p. Hum Genet. 1990 Sep;85(4):403-4. doi: 10.1007/BF02428278. Hum Genet. 1990. PMID: 2210748

6

Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups.

Daiger SP, Humphries MM, Giesenschlag N, Sharp E, McWilliam P, Farrer J, Bradley D, Kenna P, McConnell DJ, Sparkes RS, et al. Daiger SP, et al. Among authors: mcwilliam p. Cytogenet Cell Genet. 1989;50(4):181-7. doi: 10.1159/000132758. Cytogenet Cell Genet. 1989. PMID: 2572401

7

Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21.

Farrar GJ, McWilliam P, Sharp EM, Kenna P, Bradley DG, Humphries MM, McConnell DJ, Humphries P. Farrar GJ, et al. Among authors: mcwilliam p. Genomics. 1989 Oct;5(3):612-8. doi: 10.1016/0888-7543(89)90030-x. Genomics. 1989. PMID: 2613243

8

Observations on the structure of two human 7SK pseudogenes and on homologous transcripts in vertebrate species.

Humphries P, Russell SE, McWilliam P, McQuaid S, Pearson C, Humphries MM. Humphries P, et al. Among authors: mcwilliam p. Biochem J. 1987 Jul 1;245(1):281-4. doi: 10.1042/bj2450281. Biochem J. 1987. PMID: 3663152 Free PMC article.

9

Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus.

Bradley DG, Farrar GJ, Sharp EM, Kenna P, Humphries MM, McConnell DJ, Daiger SP, McWilliam P, Humphries P. Bradley DG, et al. Among authors: mcwilliam p. Am J Hum Genet. 1989 Apr;44(4):570-6. Am J Hum Genet. 1989. PMID: 2564733 Free PMC article.

10

Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.

Humphries P, Farrar GJ, Kenna P, McWilliam P. Humphries P, et al. Among authors: mcwilliam p. Clin Genet. 1990 Jul;38(1):1-13. doi: 10.1111/j.1399-0004.1990.tb03541.x. Clin Genet. 1990. PMID: 2201466 Review.

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