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MRC Human Genetics Unit,
MRC IGMM,
Western General Hospital,
MRC Human Genetics Unit, MRC IGMM, Western General Hospital
Margaret Keighren has not added Biography.
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Clonal analysis of patterns of growth, stem cell activity, and cell movement during the development and maintenance of the murine corneal epithelium.
Developmental dynamics : an official publication of the American Association of Anatomists Aug, 2002 | Pubmed ID: 12203735
Polyploid cells in the mouse ovary.
Journal of anatomy Jun, 2003 | Pubmed ID: 12846477
Evaluation of the mouse TgTP6.3 tauGFP transgene as a lineage marker in chimeras.
Journal of anatomy Jan, 2005 | Pubmed ID: 15679873
Genomic localization of a Dct-LacZ transgene locus: a simple assay for transgene status.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society Dec, 2006 | Pubmed ID: 17083491
Humanized MC1R transgenic mice reveal human specific receptor function.
Human molecular genetics Oct, 2007 | Pubmed ID: 17652101
Evaluation of triploid<-->diploid and trisomy-3<-->diploid mouse chimeras as models for investigating how lineage restriction occurs in confined placental mosaicism.
Reproduction (Cambridge, England) Dec, 2007 | Pubmed ID: 18042637
Palmitoylation regulates epidermal homeostasis and hair follicle differentiation.
PLoS genetics Nov, 2009 | Pubmed ID: 19956733
Involvement of the melanocortin-1 receptor in acute pain and pain of inflammatory but not neuropathic origin.
PloS one , 2010 | Pubmed ID: 20856883
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.
American journal of human genetics Apr, 2011 | Pubmed ID: 21473986
Evaluation of methods for one-dimensional spatial analysis of two-dimensional patterns in mouse chimaeras.
Journal of anatomy Sep, 2011 | Pubmed ID: 21615733
Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development.
Cell May, 2012 | Pubmed ID: 22579044
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
Investigative ophthalmology & visual science May, 2013 | Pubmed ID: 23633653
A trans-acting protein effect causes severe eye malformation in the Mp mouse.
PLoS genetics Dec, 2013 | Pubmed ID: 24348270
Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes.
PLoS genetics Dec, 2013 | Pubmed ID: 24415959
A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation.
PLoS genetics May, 2014 | Pubmed ID: 24809698
University of Edinburgh
Richard L. Mort1,
Margaret Keighren1,
Leonard Hay1,
Ian J. Jackson1
1MRC Human Genetics Unit, MRC IGMM, Western General Hospital, University of Edinburgh
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