Ian J. Jackson

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Dominant role of the niche in melanocyte stem-cell fate determination.

Presence of visual head tracking differentiates normal sighted from retinal degenerate mice.

Bcl2 regulation by the melanocyte master regulator Mitf modulates lineage survival and melanoma cell viability.

Neural crest progenitors of the melanocyte lineage: coat colour patterns revisited.

The promises and problems of linkage analysis by using the current canine genome map.

The structure and evolution of the melanocortin and MCH receptors in fish and mammals.

Sequence characterization of teleost fish melanocortin receptors.

Widespread tangential dispersion and extensive cell death during early neurogenesis in the mouse neocortex.

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.

Large-scale analysis of gene structure in rhodopsin-like GPCRs: evidence for widespread loss of an ancient intron.

The G-netics of dark skin.

The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis.

17th International Mouse Genome Conference.

Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor.

Genotype-phenotype correlation of mouse pde6b mutations.

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy.

Genomic anatomy of the Tyrp1 (brown) deletion complex.

Regulation of pigmentation in zebrafish melanophores.

Identifying the genes causing human diversity.

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Genomic localization of a Dct-LacZ transgene locus: a simple assay for transgene status.

Humanized MC1R transgenic mice reveal human specific receptor function.

Genetics. Beta-defensin repertoire expands.

Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development.

Expression of the fras1/frem gene family during zebrafish development and fin morphogenesis.

mc1r Pathway regulation of zebrafish melanosome dispersion.

GABAergic amacrine cells and visual function are reduced in PAC1 transgenic mice.

Palmitoylation regulates epidermal homeostasis and hair follicle differentiation.

Genetic determinants of hair and eye colours in the Scottish and Danish populations.

Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume.

Ex vivo live imaging of melanoblast migration in embryonic mouse skin.

Human beta-defensin 3 has immunosuppressive activity in vitro and in vivo.

The physiological and phenotypic determinants of human tanning measured as change in skin colour following a single dose of ultraviolet B radiation.

Involvement of the melanocortin-1 receptor in acute pain and pain of inflammatory but not neuropathic origin.

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype.

In praise of books.

A zebrafish model for nevus regeneration.

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.

Differentiated melanocyte cell division occurs in vivo and is promoted by mutations in Mitf.

Mouse genomic variation and its effect on phenotypes and gene regulation.

Rac1 drives melanoblast organization during mouse development by orchestrating pseudopod- driven motility and cell-cycle progression.

P-Rex1 is required for efficient melanoblast migration and melanoma metastasis.

Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.

Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome.

A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.

Signatures of diversifying selection in European pig breeds.

A conditional zebrafish MITF mutation reveals MITF levels are critical for melanoma promotion vs. regression in vivo.

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.

How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns.

A trans-acting protein effect causes severe eye malformation in the Mp mouse.

Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes.

Kdm3a lysine demethylase is an Hsp90 client required for cytoskeletal rearrangements during spermatogenesis.

A novel mouse model of Warburg Micro Syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton.

A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation.