Maher ER - Search Results

1

Epigenetic analysis of childhood acute lymphoblastic leukemia.

Dunwell TL, Hesson LB, Pavlova T, Zabarovska V, Kashuba V, Catchpoole D, Chiaramonte R, Brini AT, Griffiths M, Maher ER, Zabarovsky E, Latif F. Dunwell TL, et al. Among authors: maher er. Epigenetics. 2009 Apr 1;4(3):185-93. doi: 10.4161/epi.4.3.8752. Epub 2009 Apr 12. Epigenetics. 2009. PMID: 19430199

2

TaqI and PstI RFLPs in the von Hippel-Lindau disease gene (VHL).

Richards FM, Latif F, Lerman MI, Zbar B, Maher ER. Richards FM, et al. Among authors: maher er. Hum Mol Genet. 1993 Oct;2(10):1750. doi: 10.1093/hmg/2.10.1750. Hum Mol Genet. 1993. PMID: 7903582 No abstract available.

3

Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus.

Crossey PA, Maher ER, Jones MH, Richards FM, Latif F, Phipps ME, Lush M, Foster K, Tory K, Green JS, et al. Crossey PA, et al. Among authors: maher er. Hum Mol Genet. 1993 Mar;2(3):279-82. doi: 10.1093/hmg/2.3.279. Hum Mol Genet. 1993. PMID: 8499917

4

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.

Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W. Brown KW, et al. Among authors: maher er. Hum Mol Genet. 1996 Dec;5(12):2027-32. doi: 10.1093/hmg/5.12.2027. Hum Mol Genet. 1996. PMID: 8968759

5

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: maher er. J Med Genet. 1997 May;34(5):353-9. doi: 10.1136/jmg.34.5.353. J Med Genet. 1997. PMID: 9152830 Free PMC article.

6

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

Joyce JA, Lam WK, Catchpoole DJ, Jenks P, Reik W, Maher ER, Schofield PN. Joyce JA, et al. Among authors: maher er. Hum Mol Genet. 1997 Sep;6(9):1543-8. doi: 10.1093/hmg/6.9.1543. Hum Mol Genet. 1997. PMID: 9285792

7

Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer.

Fullwood P, Marchini S, Rader JS, Martinez A, Macartney D, Broggini M, Morelli C, Barbanti-Brodano G, Maher ER, Latif F. Fullwood P, et al. Among authors: maher er. Cancer Res. 1999 Sep 15;59(18):4662-7. Cancer Res. 1999. PMID: 10493522

8

Role of chromosome 3p12-p21 tumour suppressor genes in clear cell renal cell carcinoma: analysis of VHL dependent and VHL independent pathways of tumorigenesis.

Martinez A, Fullwood P, Kondo K, Kishida T, Yao M, Maher ER, Latif F. Martinez A, et al. Among authors: maher er. Mol Pathol. 2000 Jun;53(3):137-44. doi: 10.1136/mp.53.3.137. Mol Pathol. 2000. PMID: 10897333 Free PMC article.

9

Detailed mapping of a congenital heart disease gene in chromosome 3p25.

Green EK, Priestley MD, Waters J, Maliszewska C, Latif F, Maher ER. Green EK, et al. Among authors: maher er. J Med Genet. 2000 Aug;37(8):581-7. doi: 10.1136/jmg.37.8.581. J Med Genet. 2000. PMID: 10922384 Free PMC article.

10

Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.

Agathanggelou A, Honorio S, Macartney DP, Martinez A, Dallol A, Rader J, Fullwood P, Chauhan A, Walker R, Shaw JA, Hosoe S, Lerman MI, Minna JD, Maher ER, Latif F. Agathanggelou A, et al. Among authors: maher er. Oncogene. 2001 Mar 22;20(12):1509-18. doi: 10.1038/sj.onc.1204175. Oncogene. 2001. PMID: 11313894

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