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Items: 30

1.

CRX Expression in Pluripotent Stem Cell-Derived Photoreceptors Marks a Transplantable Subpopulation of Early Cones.

Collin J, Zerti D, Queen R, Santos-Ferreira T, Bauer R, Coxhead J, Hussain R, Steel D, Mellough C, Ader M, Sernagor E, Armstrong L, Lako M.

Stem Cells. 2019 May;37(5):609-622. doi: 10.1002/stem.2974. Epub 2019 Jan 30.

2.

Deconstructing Retinal Organoids: Single Cell RNA-Seq Reveals the Cellular Components of Human Pluripotent Stem Cell-Derived Retina.

Collin J, Queen R, Zerti D, Dorgau B, Hussain R, Coxhead J, Cockell S, Lako M.

Stem Cells. 2019 May;37(5):593-598. doi: 10.1002/stem.2963. Epub 2019 Jan 12.

3.

High prevalence of focal and multi-focal somatic genetic variants in the human brain.

Keogh MJ, Wei W, Aryaman J, Walker L, van den Ameele J, Coxhead J, Wilson I, Bashton M, Beck J, West J, Chen R, Haudenschild C, Bartha G, Luo S, Morris CM, Jones NS, Attems J, Chinnery PF.

Nat Commun. 2018 Oct 15;9(1):4257. doi: 10.1038/s41467-018-06331-w.

4.

Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.

Floros VI, Pyle A, Dietmann S, Wei W, Tang WWC, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, Surani MA, Chinnery PF.

Nat Cell Biol. 2018 Aug;20(8):991. doi: 10.1038/s41556-018-0064-9.

PMID:
29674682
5.

Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.

Floros VI, Pyle A, Dietmann S, Wei W, Tang WCW, Irie N, Payne B, Capalbo A, Noli L, Coxhead J, Hudson G, Crosier M, Strahl H, Khalaf Y, Saitou M, Ilic D, Surani MA, Chinnery PF.

Nat Cell Biol. 2018 Feb;20(2):144-151. doi: 10.1038/s41556-017-0017-8. Epub 2018 Jan 15. Erratum in: Nat Cell Biol. 2018 Apr 19;:.

6.

Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20).

Duncan CJA, Dinnigan E, Theobald R, Grainger A, Skelton AJ, Hussain R, Willet JDP, Swan DJ, Coxhead J, Thomas MF, Thomas J, Zamvar V, Slatter MA, Cant AJ, Engelhardt KR, Hambleton S.

Ann Rheum Dis. 2018 May;77(5):783-786. doi: 10.1136/annrheumdis-2016-210944. Epub 2017 Jun 28. No abstract available.

7.

Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.

Wei W, Keogh MJ, Wilson I, Coxhead J, Ryan S, Rollinson S, Griffin H, Kurzawa-Akanbi M, Santibanez-Koref M, Talbot K, Turner MR, McKenzie CA, Troakes C, Attems J, Smith C, Al Sarraj S, Morris CM, Ansorge O, Pickering-Brown S, Ironside JW, Chinnery PF.

Acta Neuropathol Commun. 2017 Feb 22;5(1):17. doi: 10.1186/s40478-017-0419-7. No abstract available.

8.

Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.

Wei W, Keogh MJ, Wilson I, Coxhead J, Ryan S, Rollinson S, Griffin H, Kurzawa-Akanbi M, Santibanez-Koref M, Talbot K, Turner MR, McKenzie CA, Troakes C, Attems J, Smith C, Al Sarraj S, Morris CM, Ansorge O, Pickering-Brown S, Ironside JW, Chinnery PF.

Acta Neuropathol Commun. 2017 Feb 2;5(1):13. doi: 10.1186/s40478-016-0404-6. Erratum in: Acta Neuropathol Commun. 2017 Feb 22;5(1):17.

9.

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource.

Keogh MJ, Wei W, Wilson I, Coxhead J, Ryan S, Rollinson S, Griffin H, Kurzawa-Akanbi M, Santibanez-Koref M, Talbot K, Turner MR, McKenzie CA, Troakes C, Attems J, Smith C, Al Sarraj S, Morris CM, Ansorge O, Pickering-Brown S, Ironside JW, Chinnery PF.

Genome Res. 2017 Jan;27(1):165-173. doi: 10.1101/gr.210609.116. Epub 2016 Dec 21.

10.

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development.

Lindsay SJ, Xu Y, Lisgo SN, Harkin LF, Copp AJ, Gerrelli D, Clowry GJ, Talbot A, Keogh MJ, Coxhead J, Santibanez-Koref M, Chinnery PF.

Front Neuroanat. 2016 Oct 26;10:86. eCollection 2016. No abstract available.

11.

Somatic mtDNA variation is an important component of Parkinson's disease.

Coxhead J, Kurzawa-Akanbi M, Hussain R, Pyle A, Chinnery P, Hudson G.

Neurobiol Aging. 2016 Feb;38:217.e1-217.e6. doi: 10.1016/j.neurobiolaging.2015.10.036. Epub 2015 Nov 6.

12.

Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans.

Pyle A, Hudson G, Wilson IJ, Coxhead J, Smertenko T, Herbert M, Santibanez-Koref M, Chinnery PF.

PLoS Genet. 2015 May 14;11(5):e1005040. doi: 10.1371/journal.pgen.1005040. eCollection 2015 May.

13.

Deep resequencing of mitochondrial DNA.

Payne BA, Gardner K, Coxhead J, Chinnery PF.

Methods Mol Biol. 2015;1264:59-66. doi: 10.1007/978-1-4939-2257-4_6.

PMID:
25631003
14.

Molecular pathogenesis of polymerase γ-related neurodegeneration.

Tzoulis C, Tran GT, Coxhead J, Bertelsen B, Lilleng PK, Balafkan N, Payne B, Miletic H, Chinnery PF, Bindoff LA.

Ann Neurol. 2014 Jul;76(1):66-81. doi: 10.1002/ana.24185. Epub 2014 Jun 14.

15.

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.

Pfeffer G, Gorman GS, Griffin H, Kurzawa-Akanbi M, Blakely EL, Wilson I, Sitarz K, Moore D, Murphy JL, Alston CL, Pyle A, Coxhead J, Payne B, Gorrie GH, Longman C, Hadjivassiliou M, McConville J, Dick D, Imam I, Hilton D, Norwood F, Baker MR, Jaiser SR, Yu-Wai-Man P, Farrell M, McCarthy A, Lynch T, McFarland R, Schaefer AM, Turnbull DM, Horvath R, Taylor RW, Chinnery PF.

Brain. 2014 May;137(Pt 5):1323-36. doi: 10.1093/brain/awu060. Epub 2014 Apr 10.

16.

Identification of a neuronal transcription factor network involved in medulloblastoma development.

Lastowska M, Al-Afghani H, Al-Balool HH, Sheth H, Mercer E, Coxhead JM, Redfern CP, Peters H, Burt AD, Santibanez-Koref M, Bacon CM, Chesler L, Rust AG, Adams DJ, Williamson D, Clifford SC, Jackson MS.

Acta Neuropathol Commun. 2013 Jul 11;1:35. doi: 10.1186/2051-5960-1-35.

17.

Universal heteroplasmy of human mitochondrial DNA.

Payne BA, Wilson IJ, Yu-Wai-Man P, Coxhead J, Deehan D, Horvath R, Taylor RW, Samuels DC, Santibanez-Koref M, Chinnery PF.

Hum Mol Genet. 2013 Jan 15;22(2):384-90. doi: 10.1093/hmg/dds435. Epub 2012 Oct 16.

18.

Post-transcriptional exon shuffling events in humans can be evolutionarily conserved and abundant.

Al-Balool HH, Weber D, Liu Y, Wade M, Guleria K, Nam PL, Clayton J, Rowe W, Coxhead J, Irving J, Elliott DJ, Hall AG, Santibanez-Koref M, Jackson MS.

Genome Res. 2011 Nov;21(11):1788-99. doi: 10.1101/gr.116442.110. Epub 2011 Sep 23.

19.

Differential antineoplastic effects of butyrate in cells with and without a functioning DNA mismatch repair.

Dronamraju SS, Coxhead JM, Kelly SB, Mathers JC.

Nutr Cancer. 2010;62(1):105-15. doi: 10.1080/01635580903191486.

PMID:
20043265
20.

Life without a wall or division machine in Bacillus subtilis.

Leaver M, Domínguez-Cuevas P, Coxhead JM, Daniel RA, Errington J.

Nature. 2009 Feb 12;457(7231):849-53. doi: 10.1038/nature07742.

PMID:
19212404
21.

Cell kinetics and gene expression changes in colorectal cancer patients given resistant starch: a randomised controlled trial.

Dronamraju SS, Coxhead JM, Kelly SB, Burn J, Mathers JC.

Gut. 2009 Mar;58(3):413-20. doi: 10.1136/gut.2008.162933. Epub 2008 Oct 31.

PMID:
18978177
22.

Role of DNA-mismatch repair in anti-neoplastic effects of butyrate.

Dronamraju SS, Coxhead JM, Kelly SB, Mathers JC.

Proc Nutr Soc. 2008 May;67(OCE):E87. doi: 10.1017/S0029665108007192. Review. No abstract available.

PMID:
18768094
23.

Nutrition and DNA repair--potential molecular mechanisms of action.

Mathers JC, Coxhead JM, Tyson J.

Curr Cancer Drug Targets. 2007 Aug;7(5):425-31. Review.

PMID:
17691901
24.

DNA mismatch repair status may influence anti-neoplastic effects of butyrate.

Coxhead JM, Williams EA, Mathers JC.

Biochem Soc Trans. 2005 Aug;33(Pt 4):728-9. Review.

PMID:
16042586
25.

Anti-cancer effects of butyrate: use of micro-array technology to investigate mechanisms.

Williams EA, Coxhead JM, Mathers JC.

Proc Nutr Soc. 2003 Feb;62(1):107-15. Review.

PMID:
12740065
26.

Mutations in APC, Kirsten-ras, and p53--alternative genetic pathways to colorectal cancer.

Smith G, Carey FA, Beattie J, Wilkie MJ, Lightfoot TJ, Coxhead J, Garner RC, Steele RJ, Wolf CR.

Proc Natl Acad Sci U S A. 2002 Jul 9;99(14):9433-8. Epub 2002 Jul 1.

27.
28.

Comparative biotransformation studies of MeIQx and PhIP in animal models and humans.

Garner RC, Lightfoot TJ, Cupid BC, Russell D, Coxhead JM, Kutschera W, Priller A, Rom W, Steier P, Alexander DJ, Leveson SH, Dingley KH, Mauthe RJ, Turteltaub KW.

Cancer Lett. 1999 Sep 1;143(2):161-5.

PMID:
10503897
29.

Detectable levels of serum aflatoxin B1-albumin adducts in the United Kingdom population: implications for aflatoxin-B1 exposure in the United Kingdom.

Turner PC, Dingley KH, Coxhead J, Russell S, Garner CR.

Cancer Epidemiol Biomarkers Prev. 1998 May;7(5):441-7.

30.

Cervical cancer screening by women's health nurses.

Coxhead JI.

Aust J Public Health. 1993 Mar;17(1):79. No abstract available.

PMID:
8357903

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