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Items: 31

1.

Macrophage-Derived IL1β and TNFα Regulate Arginine Metabolism in Neuroblastoma.

Fultang L, Gamble LD, Gneo L, Berry AM, Egan SA, De Bie F, Yogev O, Eden GL, Booth S, Brownhill S, Vardon A, McConville CM, Cheng PN, Norris MD, Etchevers HC, Murray J, Ziegler DS, Chesler L, Schmidt R, Burchill SA, Haber M, De Santo C, Mussai F.

Cancer Res. 2019 Feb 1;79(3):611-624. doi: 10.1158/0008-5472.CAN-18-2139. Epub 2018 Dec 13.

PMID:
30545920
2.

Metabolite profiling in retinoblastoma identifies novel clinicopathological subgroups.

Kohe S, Brundler MA, Jenkinson H, Parulekar M, Wilson M, Peet AC, McConville CM; Children’s Cancer and Leukaemia Group.

Br J Cancer. 2015 Oct 20;113(8):1216-24. doi: 10.1038/bjc.2015.318. Epub 2015 Sep 8.

3.

Gene expression profiling identifies different sub-types of retinoblastoma.

Kapatai G, Brundler MA, Jenkinson H, Kearns P, Parulekar M, Peet AC, McConville CM.

Br J Cancer. 2013 Jul 23;109(2):512-25. doi: 10.1038/bjc.2013.283. Epub 2013 Jun 11.

4.

Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma.

Chughtai SA, Genus T, Ramani P, Dyer S, Powell JE, McMullan D, Davison V, McConville CM; UK Children's Cancer Study Group.

Eur J Cancer. 2006 Aug;42(12):1826-34. Epub 2006 Jul 26.

PMID:
16872824
5.

Neuroblastoma - a developmental perspective.

McConville CM, Forsyth J.

Cancer Lett. 2003 Jul 18;197(1-2):3-9. Review.

PMID:
12880953
6.

Weak linkage at 4p16 to predisposition for human neuroblastoma.

Perri P, Longo L, Cusano R, McConville CM, Rees SA, Devoto M, Conte M, Ferrara GB, Seri M, Romeo G, Tonini GP.

Oncogene. 2002 Nov 28;21(54):8356-60.

7.

Molecular analysis of single colonies reveals a diverse origin of initial clonal proliferation in B-precursor acute lymphoblastic leukemia that can precede the t(12;21) translocation.

Weston VJ, McConville CM, Mann JR, Darbyshire PJ, Lawson S, Gordon J, Moss PA, Taylor AM, Stankovic T.

Cancer Res. 2001 Dec 1;61(23):8547-53.

8.

Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17).

McConville CM, Dyer S, Rees SA, Luttikhuis ME, McMullan DJ, Vickers SJ, Ramani P, Redfern D, Morland BJ.

Cancer Genet Cytogenet. 2001 Oct 15;130(2):133-40.

PMID:
11675134
9.

Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis.

Luttikhuis ME, Powell JE, Rees SA, Genus T, Chughtai S, Ramani P, Mann JR, McConville CM.

Br J Cancer. 2001 Aug 17;85(4):531-7.

10.

Detection of MYCN amplification in neuroblastoma using competitive PCR quantitation.

Oude Luttikhuis ME, Iyer VK, Dyer S, Ramani P, McConville CM.

Lab Invest. 2000 Feb;80(2):271-3. No abstract available.

PMID:
10701696
11.

Clonal diversity of Ig and T-cell receptor gene rearrangements in childhood B-precursor acute lymphoblastic leukaemia.

Stankovic T, Weston V, McConville CM, Green E, Powell JE, Mann JR, Darbyshire PJ, Taylor AM.

Leuk Lymphoma. 2000 Jan;36(3-4):213-24. Review.

PMID:
10674894
12.
13.

Construction of a transcription map around the gene for ataxia telangiectasia: identification of at least four novel genes.

Stankovic T, Byrd PJ, Cooper PR, McConville CM, Munroe DJ, Riley JH, Watts GD, Ambrose H, McGuire G, Smith AD, Sutcliffe A, Mills T, Taylor AM.

Genomics. 1997 Mar 1;40(2):267-76.

PMID:
9119394
14.

Identification and analysis of expression of human VACM-1, a cullin gene family member located on chromosome 11q22-23.

Byrd PJ, Stankovic T, McConville CM, Smith AD, Cooper PR, Taylor AM.

Genome Res. 1997 Jan;7(1):71-5.

15.

Mutations associated with variant phenotypes in ataxia-telangiectasia.

McConville CM, Stankovic T, Byrd PJ, McGuire GM, Yao QY, Lennox GG, Taylor MR.

Am J Hum Genet. 1996 Aug;59(2):320-30.

16.

Mutations revealed by sequencing the 5' half of the gene for ataxia telangiectasia.

Byrd PJ, McConville CM, Cooper P, Parkhill J, Stankovic T, McGuire GM, Thick JA, Taylor AM.

Hum Mol Genet. 1996 Jan;5(1):145-9.

PMID:
8789452
17.

Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome.

Green AJ, Yates JR, Taylor AM, Biggs P, McGuire GM, McConville CM, Billing CJ, Barnes ND.

Arch Dis Child. 1995 Nov;73(5):431-4.

18.

Genetic and physical mapping of the ataxia-telangiectasia locus on chromosome 11q22-q23.

McConville CM, Byrd PJ, Ambrose HJ, Taylor AM.

Int J Radiat Biol. 1994 Dec;66(6 Suppl):S45-56. Review.

PMID:
7836852
19.

A haplotype common to intermediate radiosensitivity variants of ataxia-telangiectasia in the UK.

Taylor AM, McConville CM, Rotman G, Shiloh Y, Byrd PJ.

Int J Radiat Biol. 1994 Dec;66(6 Suppl):S35-41.

PMID:
7836851
20.

Sixth international workshop on ataxia-telangiectasia.

Gatti RA, McConville CM, Taylor AM.

Cancer Res. 1994 Nov 15;54(22):6007-10. No abstract available.

21.

Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3.

Farndon PA, Morris DJ, Hardy C, McConville CM, Weissenbach J, Kilpatrick MW, Reis A.

Genomics. 1994 Sep 15;23(2):486-9.

PMID:
7835901
22.

Cancer and DNA processing disorders.

Taylor AM, McConville CM, Byrd PJ.

Br Med Bull. 1994 Jul;50(3):708-17. Review.

PMID:
7987650
23.

A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasia.

Ambrose HJ, Byrd PJ, McConville CM, Cooper PR, Stankovic T, Riley JH, Shiloh Y, McNamara JO, Fukao T, Taylor AM.

Genomics. 1994 Jun;21(3):612-9.

PMID:
7959739
24.

Genetic and cellular features of ataxia telangiectasia.

Taylor AM, Byrd PJ, McConville CM, Thacker S.

Int J Radiat Biol. 1994 Jan;65(1):65-70. Review.

PMID:
7905911
25.

Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23.

McConville CM, Byrd PJ, Ambrose HJ, Stankovic T, Ziv Y, Bar-Shira A, Vanagaite L, Rotman G, Shiloh Y, Gillett GT, et al.

Hum Mol Genet. 1993 Jul;2(7):969-74.

PMID:
8364579
26.

The order and orientation of a cluster of metalloproteinase genes, stromelysin 2, collagenase, and stromelysin, together with D11S385, on chromosome 11q22-q23.

Formstone CJ, Byrd PJ, Ambrose HJ, Riley JH, Hernandez D, McConville CM, Taylor AM.

Genomics. 1993 Apr;16(1):289-91.

PMID:
8486377
27.

Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23.

Gillett GT, McConville CM, Byrd PJ, Stankovic T, Taylor AM, Hunt DM, West LF, Fox MF, Povey S, Benham FJ.

Genomics. 1993 Feb;15(2):332-41.

PMID:
8449499
28.

A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23.

Hernandez D, McConville CM, Stacey M, Woods CG, Brown MM, Shutt P, Rysiecki G, Taylor AM.

J Med Genet. 1993 Feb;30(2):135-40.

29.
31.

Analysis of 7 polymorphic markers at chromosome 11q22-23 in 35 ataxia telangiectasia families; further evidence of linkage.

McConville CM, Woods CG, Farrall M, Metcalfe JA, Taylor AM.

Hum Genet. 1990 Jul;85(2):215-20.

PMID:
2370052

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