Ian J. Jackson

MRC Human Genetics Unit, University of Edinburgh

Research Area

Biography

Ian J. Jackson has not added Biography.
If you are Ian J. Jackson and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 11	2014

Other Publications

Article	Year
Novel ENU-induced eye mutations in the mouse: models for human eye disease. Human molecular genetics\| PubMed ID: 11929848	2002
Dominant role of the niche in melanocyte stem-cell fate determination. Nature\| PubMed ID: 11976685	2002
Presence of visual head tracking differentiates normal sighted from retinal degenerate mice. Neuroscience letters\| PubMed ID: 12023058	2002
Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability. Cell\| PubMed ID: 12086670	2002
Neural crest progenitors of the melanocyte lineage: coat colour patterns revisited. Development (Cambridge, England)\| PubMed ID: 12091305	2002
The promises and problems of linkage analysis by using the current canine genome map. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 12461654	2002
The structure and evolution of the melanocortin and MCH receptors in fish and mammals. Genomics\| PubMed ID: 12620396	2003
Sequence characterization of teleost fish melanocortin receptors. Annals of the New York Academy of Sciences\| PubMed ID: 12851332	2003
Widespread tangential dispersion and extensive cell death during early neurogenesis in the mouse neocortex. Developmental biology\| PubMed ID: 14975720	2004
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome. Human molecular genetics\| PubMed ID: 15150159	2004
Large-scale analysis of gene structure in rhodopsin-like GPCRs: evidence for widespread loss of an ancient intron. Gene\| PubMed ID: 15302402	2004
The G-netics of dark skin. Nature genetics\| PubMed ID: 15340429	2004
The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 15345741	2004
17th International Mouse Genome Conference. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 15366370	2004
Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 15366372	2004
Genotype-phenotype correlation of mouse pde6b mutations. Investigative ophthalmology & visual science\| PubMed ID: 16123450	2005
Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy. Human molecular genetics\| PubMed ID: 16159887	2005
Genomic anatomy of the Tyrp1 (brown) deletion complex. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 16505357	2006
Regulation of pigmentation in zebrafish melanophores. Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society\| PubMed ID: 16704454	2006
Identifying the genes causing human diversity. European journal of human genetics : EJHG\| PubMed ID: 16723996	2006
Cardiac malformations and midline skeletal defects in mice lacking filamin A. Human molecular genetics\| PubMed ID: 16825286	2006
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\| PubMed ID: 17083491	2006
Humanized MC1R transgenic mice reveal human specific receptor function. Human molecular genetics\| PubMed ID: 17652101	2007
Genetics. Beta-defensin repertoire expands. Science (New York, N.Y.)\| PubMed ID: 18048676	2007
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development. Journal of cell science\| PubMed ID: 18765564	2008
Expression of the fras1/frem gene family during zebrafish development and fin morphogenesis. Developmental dynamics : an official publication of the American Association of Anatomists\| PubMed ID: 18816440	2008
mc1r Pathway regulation of zebrafish melanosome dispersion. Zebrafish\| PubMed ID: 19133827	2008
GABAergic amacrine cells and visual function are reduced in PAC1 transgenic mice. Neuropharmacology\| PubMed ID: 19596361	2010
Palmitoylation regulates epidermal homeostasis and hair follicle differentiation. PLoS genetics\| PubMed ID: 19956733	2009
Genetic determinants of hair and eye colours in the Scottish and Danish populations. BMC genetics\| PubMed ID: 20042077	2009
Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume. Human molecular genetics\| PubMed ID: 20056676	2010
Ex vivo live imaging of melanoblast migration in embryonic mouse skin. Pigment cell & melanoma research\| PubMed ID: 20067551	2010
Human beta-defensin 3 has immunosuppressive activity in vitro and in vivo. European journal of immunology\| PubMed ID: 20104491	2010
The physiological and phenotypic determinants of human tanning measured as change in skin colour following a single dose of ultraviolet B radiation. Experimental dermatology\| PubMed ID: 20648713	2010
Involvement of the melanocortin-1 receptor in acute pain and pain of inflammatory but not neuropathic origin. PloS one\| PubMed ID: 20856883	2010
The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype. Human molecular genetics\| PubMed ID: 20943750	2011
In praise of books. Pigment cell & melanoma research\| PubMed ID: 21129162	2010
A zebrafish model for nevus regeneration. Pigment cell & melanoma research\| PubMed ID: 21324102	2011
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis. American journal of human genetics\| PubMed ID: 21473986	2011
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice. PLoS genetics\| PubMed ID: 21750680	2011
Differentiated melanocyte cell division occurs in vivo and is promoted by mutations in Mitf. Development (Cambridge, England)\| PubMed ID: 21771814	2011
Mouse genomic variation and its effect on phenotypes and gene regulation. Nature\| PubMed ID: 21921910	2011
Rac1 drives melanoblast organization during mouse development by orchestrating pseudopod- driven motility and cell-cycle progression. Developmental cell\| PubMed ID: 21924960	2011
P-Rex1 is required for efficient melanoblast migration and melanoma metastasis. Nature communications\| PubMed ID: 22109529	2011
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development. The Journal of investigative dermatology\| PubMed ID: 22572819	2012
Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome. Human mutation\| PubMed ID: 23420520	2013
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy. Investigative ophthalmology & visual science\| PubMed ID: 23633653	2013
Signatures of diversifying selection in European pig breeds. PLoS genetics\| PubMed ID: 23637623	2013
A conditional zebrafish MITF mutation reveals MITF levels are critical for melanoma promotion vs. regression in vivo. The Journal of investigative dermatology\| PubMed ID: 23831555	2014
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. Genome biology\| PubMed ID: 23902802	2013
How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns. Pigment cell & melanoma research\| PubMed ID: 23923821	2013
A trans-acting protein effect causes severe eye malformation in the Mp mouse. PLoS genetics\| PubMed ID: 24348270	2013
Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes. PLoS genetics\| PubMed ID: 24415959	2013
Kdm3a lysine demethylase is an Hsp90 client required for cytoskeletal rearrangements during spermatogenesis. Molecular biology of the cell\| PubMed ID: 24554764	2014
A novel mouse model of Warburg Micro Syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton. Disease models & mechanisms\| PubMed ID: 24764192	2014
A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation. PLoS genetics\| PubMed ID: 24809698	2014