Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 32

1.

Identification of reference genes suitable for RT-qPCR studies of murine gastrulation and patterning.

Barratt KS, Diamand KEM, Arkell RM.

Mamm Genome. 2018 Oct;29(9-10):656-662. doi: 10.1007/s00335-018-9769-0. Epub 2018 Aug 9.

PMID:
30094508
2.

ZIC2 in Holoprosencephaly.

Barratt KS, Arkell RM.

Adv Exp Med Biol. 2018;1046:269-299. doi: 10.1007/978-981-10-7311-3_14. Review.

PMID:
29442327
3.

Overview of Rodent Zic Genes.

Diamand KEM, Barratt KS, Arkell RM.

Adv Exp Med Biol. 2018;1046:179-207. doi: 10.1007/978-981-10-7311-3_10. Review.

PMID:
29442323
4.

Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling.

Houtmeyers R, Tchouate Gainkam O, Glanville-Jones HA, Van den Bosch B, Chappell A, Barratt KS, Souopgui J, Tejpar S, Arkell RM.

Hum Mol Genet. 2016 Sep 15;25(18):3946-3959. doi: 10.1093/hmg/ddw235. Epub 2016 Jul 27.

PMID:
27466203
5.

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes.

Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Tuy FP, Chelly J, Morris HD, Riegler J, Lythgoe MF, Arkell RM, Loreni F, Flint J, Pavan WJ, Keays DA.

PLoS Genet. 2015 Nov 19;11(11):e1005682. doi: 10.1371/journal.pgen.1005682. eCollection 2015 Nov. No abstract available.

6.

Flightless I is a key regulator of the fibroproliferative process in hypertrophic scarring and a target for a novel antiscarring therapy.

Cameron AM, Turner CT, Adams DH, Jackson JE, Melville E, Arkell RM, Anderson PJ, Cowin AJ.

Br J Dermatol. 2016 Apr;174(4):786-94. doi: 10.1111/bjd.14263. Epub 2016 Jan 9.

PMID:
26521845
7.

Fibroblast-specific upregulation of Flightless I impairs wound healing.

Turner CT, Waters JM, Jackson JE, Arkell RM, Cowin AJ.

Exp Dermatol. 2015 Sep;24(9):692-7. doi: 10.1111/exd.12751. Epub 2015 Jul 14.

PMID:
25959103
8.

The role of Zic genes in inner ear development in the mouse: Exploring mutant mouse phenotypes.

Chervenak AP, Bank LM, Thomsen N, Glanville-Jones HC, Jonathan S, Millen KJ, Arkell RM, Barald KF.

Dev Dyn. 2014 Nov;243(11):1487-98. doi: 10.1002/dvdy.24186. Epub 2014 Sep 16.

9.

The Zic2 gene directs the formation and function of node cilia to control cardiac situs.

Barratt KS, Glanville-Jones HC, Arkell RM.

Genesis. 2014 Jun;52(6):626-35. doi: 10.1002/dvg.22767. Epub 2014 Mar 17.

PMID:
24585447
10.

Flightless I over-expression impairs skin barrier development, function and recovery following skin blistering.

Kopecki Z, Yang GN, Arkell RM, Jackson JE, Melville E, Iwata H, Ludwig RJ, Zillikens D, Murrell DF, Cowin AJ.

J Pathol. 2014 Apr;232(5):541-52. doi: 10.1002/path.4323. Epub 2014 Feb 5.

PMID:
24375017
11.

Attenuation of flightless I improves wound healing and enhances angiogenesis in a murine model of type 1 diabetes.

Ruzehaji N, Kopecki Z, Melville E, Appleby SL, Bonder CS, Arkell RM, Fitridge R, Cowin AJ.

Diabetologia. 2014 Feb;57(2):402-12. doi: 10.1007/s00125-013-3107-6. Epub 2013 Nov 29.

PMID:
24292564
12.

Wnt signalling in mouse gastrulation and anterior development: new players in the pathway and signal output.

Arkell RM, Fossat N, Tam PP.

Curr Opin Genet Dev. 2013 Aug;23(4):454-60. doi: 10.1016/j.gde.2013.03.001. Epub 2013 Apr 19. Review.

PMID:
23608663
13.

Successful whole embryo culture with commercially available reagents.

Glanville-Jones HC, Woo N, Arkell RM.

Int J Dev Biol. 2013;57(1):61-7. doi: 10.1387/ijdb.120098ra.

14.

A murine Zic3 transcript with a premature termination codon evades nonsense-mediated decay during axis formation.

Ahmed JN, Ali RG, Warr N, Wilson HM, Bellchambers HM, Barratt KS, Thompson AJ, Arkell RM.

Dis Model Mech. 2013 May;6(3):755-67. doi: 10.1242/dmm.011668. Epub 2013 Feb 21.

15.

Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.

Caruana G, Farlie PG, Hart AH, Bagheri-Fam S, Wallace MJ, Dobbie MS, Gordon CT, Miller KA, Whittle B, Abud HE, Arkell RM, Cole TJ, Harley VR, Smyth IM, Bertram JF.

PLoS One. 2013;8(3):e55429. doi: 10.1371/journal.pone.0055429. Epub 2013 Mar 1.

16.

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes.

Watkins-Chow DE, Cooke J, Pidsley R, Edwards A, Slotkin R, Leeds KE, Mullen R, Baxter LL, Campbell TG, Salzer MC, Biondini L, Gibney G, Phan Dinh Tuy F, Chelly J, Morris HD, Riegler J, Lythgoe MF, Arkell RM, Loreni F, Flint J, Pavan WJ, Keays DA.

PLoS Genet. 2013;9(1):e1003094. doi: 10.1371/journal.pgen.1003094. Epub 2013 Jan 31. Erratum in: PLoS Genet. 2015 Nov;11(11):e1005682.

17.

High resolution melt analysis (HRMA); a viable alternative to agarose gel electrophoresis for mouse genotyping.

Thomsen N, Ali RG, Ahmed JN, Arkell RM.

PLoS One. 2012;7(9):e45252. doi: 10.1371/journal.pone.0045252. Epub 2012 Sep 19.

18.

Zinc fingers of the cerebellum (Zic): transcription factors and co-factors.

Ali RG, Bellchambers HM, Arkell RM.

Int J Biochem Cell Biol. 2012 Nov;44(11):2065-8. doi: 10.1016/j.biocel.2012.08.012. Epub 2012 Aug 14. Review.

PMID:
22964024
19.

Initiating head development in mouse embryos: integrating signalling and transcriptional activity.

Arkell RM, Tam PP.

Open Biol. 2012 Mar;2(3):120030. doi: 10.1098/rsob.120030.

20.

Overexpression of the Flii gene increases dermal-epidermal blistering in an autoimmune ColVII mouse model of epidermolysis bullosa acquisita.

Kopecki Z, Arkell RM, Strudwick XL, Hirose M, Ludwig RJ, Kern JS, Bruckner-Tuderman L, Zillikens D, Murrell DF, Cowin AJ.

J Pathol. 2011 Nov;225(3):401-13. doi: 10.1002/path.2973. Epub 2011 Sep 26.

PMID:
21984127
21.

Mouse strains for the ubiquitous or conditional overexpression of the Flii gene.

Thomsen N, Chappell A, Ali RG, Jones T, Adams DH, Matthaei KI, Campbell HD, Cowin AJ, Arkell RM.

Genesis. 2011 Aug;49(8):681-8. doi: 10.1002/dvg.20735. Epub 2011 Jul 22.

PMID:
21786402
22.

Regulation of focal adhesions by flightless i involves inhibition of paxillin phosphorylation via a Rac1-dependent pathway.

Kopecki Z, O'Neill GM, Arkell RM, Cowin AJ.

J Invest Dermatol. 2011 Jul;131(7):1450-9. doi: 10.1038/jid.2011.69. Epub 2011 Mar 24.

23.

Decreased expression of Flightless I, a gelsolin family member and developmental regulator, in early-gestation fetal wounds improves healing.

Lin CH, Waters JM, Powell BC, Arkell RM, Cowin AJ.

Mamm Genome. 2011 Jun;22(5-6):341-52. doi: 10.1007/s00335-011-9320-z. Epub 2011 Mar 13.

PMID:
21400204
24.

Regeneration of hair follicles is modulated by flightless I (Flii) in a rodent vibrissa model.

Waters JM, Lindo JE, Arkell RM, Cowin AJ.

J Invest Dermatol. 2011 Apr;131(4):838-47. doi: 10.1038/jid.2010.393. Epub 2010 Dec 30.

25.

Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.

Warr N, Powles-Glover N, Chappell A, Robson J, Norris D, Arkell RM.

Hum Mol Genet. 2008 Oct 1;17(19):2986-96. doi: 10.1093/hmg/ddn197. Epub 2008 Jul 9.

PMID:
18617531
26.

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.

Bogani D, Willoughby C, Davies J, Kaur K, Mirza G, Paudyal A, Haines H, McKeone R, Cadman M, Pieles G, Schneider JE, Bhattacharya S, Hardy A, Nolan PM, Tripodis N, Depew MJ, Chandrasekara R, Duncan G, Sharpe PT, Greenfield A, Denny P, Brown SD, Ragoussis J, Arkell RM.

Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12477-82. Epub 2005 Aug 18.

27.

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.

Curtin JA, Quint E, Tsipouri V, Arkell RM, Cattanach B, Copp AJ, Henderson DJ, Spurr N, Stanier P, Fisher EM, Nolan PM, Steel KP, Brown SD, Gray IC, Murdoch JN.

Curr Biol. 2003 Jul 1;13(13):1129-33.

28.

Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.

Arkell RM, Cadman M, Marsland T, Southwell A, Thaung C, Davies JR, Clay T, Beechey CV, Evans EP, Strivens MA, Brown SD, Denny P.

Mamm Genome. 2001 Sep;12(9):687-94.

PMID:
11641716
29.

Reappearance of the minor alpha-sarcomeric actins in postnatal muscle.

Collins T, Joya JE, Arkell RM, Ferguson V, Hardeman EC.

Am J Physiol. 1997 Dec;273(6):C1801-10. doi: 10.1152/ajpcell.1997.273.6.C1801.

PMID:
9435483
30.

Stabilization of Xist RNA mediates initiation of X chromosome inactivation.

Sheardown SA, Duthie SM, Johnston CM, Newall AE, Formstone EJ, Arkell RM, Nesterova TB, Alghisi GC, Rastan S, Brockdorff N.

Cell. 1997 Oct 3;91(1):99-107.

31.

Isolation of novel tissue-specific genes from cDNA libraries representing the individual tissue constituents of the gastrulating mouse embryo.

Harrison SM, Dunwoodie SL, Arkell RM, Lehrach H, Beddington RS.

Development. 1995 Aug;121(8):2479-89.

32.

Multiple regions of the human cardiac actin gene are necessary for maturation-based expression in striated muscle.

Dunwoodie SL, Joya JE, Arkell RM, Hardeman EC.

J Biol Chem. 1994 Apr 22;269(16):12212-9.

Supplemental Content

Loading ...
Support Center