about
Initial sequencing and comparative analysis of the mouse genomeHuman and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisBcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viabilityHEATR2 plays a conserved role in assembly of the ciliary motile apparatusA second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locusThe extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermisA reappraisal of non-consensus mRNA splice sitesThe European dimension for the mouse genome mutagenesis programDiphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentThe melanocyte lineage in development and diseaseAcute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypesNovel gene function revealed by mouse mutagenesis screens for models of age-related disease.Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical modelLoss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and miceAnalysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAsIdentification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebsA trans-acting protein effect causes severe eye malformation in the Mp mouseMelanocortin 1 receptor variants in an Irish populationMouse genomic variation and its effect on phenotypes and gene regulationGenetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep.A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.Differentiated melanocyte cell division occurs in vivo and is promoted by mutations in Mitf.Rac1 drives melanoblast organization during mouse development by orchestrating pseudopod- driven motility and cell-cycle progression.Genetic determinants of hair and eye colours in the Scottish and Danish populations.A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeletonInvolvement of the melanocortin-1 receptor in acute pain and pain of inflammatory but not neuropathic origin.The mahogany mouse mutation: further links between pigmentation, obesity and the immune system.Characterization of TRP-1 mRNA levels in dominant and recessive mutations at the mouse brown (b) locus.Molecular genetics of the brown (b)-locus region of mouse chromosome 4. I. Origin and molecular mapping of radiation- and chemical-induced lethal brown deletions.The structure and evolution of the melanocortin and MCH receptors in fish and mammals.Sequence characterization of teleost fish melanocortin receptors.Regulation of pigmentation in zebrafish melanophores.Functional variation of MC1R alleles from red-haired individuals.P-Rex1 is required for efficient melanoblast migration and melanoma metastasis.Ex vivo culture of mouse embryonic skin and live-imaging of melanoblast migrationHomologous pigmentation mutations in human, mouse and other model organisms.Genomic anatomy of the Tyrp1 (brown) deletion complex.Signatures of diversifying selection in European pig breeds.mc1r Pathway regulation of zebrafish melanosome dispersion.
P50
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P50
description
professor of genetics
@en
name
Ian Jackson
@ast
Ian Jackson
@en
Ian Jackson
@es
Ian Jackson
@nl
Ian Jackson
@sl
type
label
Ian Jackson
@ast
Ian Jackson
@en
Ian Jackson
@es
Ian Jackson
@nl
Ian Jackson
@sl
altLabel
Ian J. Jackson Ph.D. F.R.S.E.
@en
prefLabel
Ian Jackson
@ast
Ian Jackson
@en
Ian Jackson
@es
Ian Jackson
@nl
Ian Jackson
@sl
P106
P21
P31
P496
0000-0001-6526-0688