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1.

Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data.

Easteal, Simon; Arkell, Ruth M; Balboa, Renzo F; Bellingham, Shayne A; Brown, Alex D; Calma, Tom; Cook, Matthew C; Davis, Megan; Dawkins, Hugh J S; Dinger, Marcel E; Dobbie, Michael S; Farlow, Ashley; Gwynne, Kylie G; Hermes, Azure; Hoy, Wendy E; Jenkins, Misty R; Jiang, Simon H; Kaplan, Warren; Leslie, Stephen; Llamas, Bastien; Mann, Graham J; McMorran, Brendan J; McWhirter, Rebekah E; Meldrum, Cliff J; Nagaraj, Shivashankar H; Newman, Saul J; Nunn, Jack S; Ormond-Parker, Lyndon; Orr, Neil J; Paliwal, Devashi; Patel, Hardip R; Pearson, Glenn; Pratt, Greg R; Rambaldini, Boe; Russell, Lynette W; Savarirayan, Ravi; Silcocks, Matthew; Skinner, John C; Souilmi, Yassine; Vinuesa, Carola G; Baynam, Gareth.

Am J Hum Genet; 107(2): 175-182, 2020 08 06.

Artículo en Inglés | MEDLINE | ID: mdl-32763188

2.

WNT-responsive SUMOylation of ZIC5 promotes murine neural crest cell development, having multiple effects on transcription.

Ali, Radiya G; Bellchambers, Helen M; Warr, Nicholas; Ahmed, Jehangir N; Barratt, Kristen S; Neill, Kieran; Diamand, Koula E M; Arkell, Ruth M.

J Cell Sci; 134(9)2021 05 01.

Artículo en Inglés | MEDLINE | ID: mdl-33771929

3.

SUMOylation Potentiates ZIC Protein Activity to Influence Murine Neural Crest Cell Specification.

Bellchambers, Helen M; Barratt, Kristen S; Diamand, Koula E M; Arkell, Ruth M.

Int J Mol Sci; 22(19)2021 Sep 28.

Artículo en Inglés | MEDLINE | ID: mdl-34638777

4.

Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling.

Houtmeyers, Rob; Tchouate Gainkam, Olive; Glanville-Jones, Hannah A; Van den Bosch, Ben; Chappell, Anna; Barratt, Kristen S; Souopgui, Jacob; Tejpar, Sabine; Arkell, Ruth M.

Hum Mol Genet; 25(18): 3946-3959, 2016 09 15.

Artículo en Inglés | MEDLINE | ID: mdl-27466203

5.

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

Barratt, Kristen S; Diamand, Koula E M; Arkell, Ruth M.

Mamm Genome; 29(9-10): 656-662, 2018 10.

Artículo en Inglés | MEDLINE | ID: mdl-30094508

6.

ZIC2 in Holoprosencephaly.

Barratt, Kristen S; Arkell, Ruth M.

Adv Exp Med Biol; 1046: 269-299, 2018.

Artículo en Inglés | MEDLINE | ID: mdl-29442327

7.

Overview of Rodent Zic Genes.

Diamand, Koula E M; Barratt, Kristen S; Arkell, Ruth M.

Adv Exp Med Biol; 1046: 179-207, 2018.

Artículo en Inglés | MEDLINE | ID: mdl-29442323

8.

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

Watkins-Chow, Dawn E; Cooke, Joanna; Pidsley, Ruth; Edwards, Andrew; Slotkin, Rebecca; Leeds, Karen E; Mullen, Raymond; Baxter, Laura L; Campbell, Thomas G; Salzer, Marion C; Biondini, Laura; Gibney, Gretchen; Phan Dinh Tuy, Françoise; Chelly, Jamel; Morris, H Douglas; Riegler, Johannes; Lythgoe, Mark F; Arkell, Ruth M; Loreni, Fabrizio; Flint, Jonathan; Pavan, William J; Keays, David A.

PLoS Genet; 9(1): e1003094, 2013.

Artículo en Inglés | MEDLINE | ID: mdl-23382688

9.

Fibroblast-specific upregulation of Flightless I impairs wound healing.

Turner, Christopher T; Waters, James M; Jackson, Jessica E; Arkell, Ruth M; Cowin, Allison J.

Exp Dermatol; 24(9): 692-7, 2015 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-25959103

10.

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

Kopecki, Zlatko; Yang, Gink N; Arkell, Ruth M; Jackson, Jessica E; Melville, Elizabeth; Iwata, Hiroaki; Ludwig, Ralf J; Zillikens, Detlef; Murrell, Dedee F; Cowin, Allison J.

J Pathol; 232(5): 541-52, 2014 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-24375017

11.

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

Chervenak, Andrew P; Bank, Lisa M; Thomsen, Nicole; Glanville-Jones, Hannah C; Jonathan, Skibo; Millen, Kathleen J; Arkell, Ruth M; Barald, Kate F.

Dev Dyn; 243(11): 1487-98, 2014 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-25178196

12.

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

Barratt, Kristen S; Glanville-Jones, Hannah C; Arkell, Ruth M.

Genesis; 52(6): 626-35, 2014 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-24585447

13.

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

Ruzehaji, Nadira; Kopecki, Zlatko; Melville, Elizabeth; Appleby, Sarah L; Bonder, Claudine S; Arkell, Ruth M; Fitridge, Robert; Cowin, Allison J.

Diabetologia; 57(2): 402-12, 2014 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-24292564

14.

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

Watkins-Chow, Dawn E; Cooke, Joanna; Pidsley, Ruth; Edwards, Andrew; Slotkin, Rebecca; Leeds, Karen E; Mullen, Raymond; Baxter, Laura L; Campbell, Thomas G; Salzer, Marion C; Biondini, Laura; Gibney, Gretchen; Tuy, Françoise Phan Dinh; Chelly, Jamel; Morris, H Douglas; Riegler, Johannes; Lythgoe, Mark F; Arkell, Ruth M; Loreni, Fabrizio; Flint, Jonathan; Pavan, William J; Keays, David A.

PLoS Genet; 11(11): e1005682, 2015 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-26584186

15.

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

Kopecki, Zlatko; Arkell, Ruth M; Strudwick, Xanthe L; Hirose, Misa; Ludwig, Ralf J; Kern, Johannes S; Bruckner-Tuderman, Leena; Zillikens, Detlef; Murrell, Dedee F; Cowin, Allison J.

J Pathol; 225(3): 401-13, 2011 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-21984127

16.

Patterning of the antero-ventral mammalian brain: Lessons from holoprosencephaly comparative biology in man and mouse.

Barratt, Kristen S; Drover, Kyle A; Thomas, Zoe M; Arkell, Ruth M.

WIREs Mech Dis; 14(4): e1552, 2022 07.

Artículo en Inglés | MEDLINE | ID: mdl-35137563

17.

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

Thomsen, Nicole; Chappell, Anna; Ali, Radiya G; Jones, Tamsin; Adams, Damian H; Matthaei, Klaus I; Campbell, Hugh D; Cowin, Allison J; Arkell, Ruth M.

Genesis; 49(8): 681-8, 2011 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-21786402

18.

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

Lin, Cheng-Hung; Waters, James M; Powell, Barry C; Arkell, Ruth M; Cowin, Allison J.

Mamm Genome; 22(5-6): 341-52, 2011 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-21400204

19.

Disruption of entire Cables2 locus leads to embryonic lethality by diminished Rps21 gene expression and enhanced p53 pathway.

Dinh, Tra Thi Huong; Iseki, Hiroyoshi; Mizuno, Seiya; Iijima-Mizuno, Saori; Tanimoto, Yoko; Daitoku, Yoko; Kato, Kanako; Hamada, Yuko; Hasan, Ammar Shaker Hamed; Suzuki, Hayate; Murata, Kazuya; Muratani, Masafumi; Ema, Masatsugu; Kim, Jun-Dal; Ishida, Junji; Fukamizu, Akiyoshi; Kato, Mitsuyasu; Takahashi, Satoru; Yagami, Ken-Ichi; Wilson, Valerie; Arkell, Ruth M; Sugiyama, Fumihiro.

Elife; 102021 05 05.

Artículo en Inglés | MEDLINE | ID: mdl-33949947

20.

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

Warr, Nicholas; Powles-Glover, Nicola; Chappell, Anna; Robson, Joan; Norris, Dominic; Arkell, Ruth M.

Hum Mol Genet; 17(19): 2986-96, 2008 Oct 01.

Artículo en Inglés | MEDLINE | ID: mdl-18617531

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