I. Jackson

发表

The European dimension for the mouse genome mutagenesis program

Steve D. M. Brown, J. Thornton, A. Ballabio, 2004 .

Initial sequencing and comparative analysis of the mouse genome.

Colin N. Dewey, Simon C. Potter, James A. Cuff, 2002 .

Mouse genomic variation and its effect on phenotypes and gene regulation

Thomas M. Keane, R. Durbin, E. Birney, 2011, Nature.

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

E. Birney, E. Lander, C. Bult, 2002, Nature.

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

I. Jackson, R. Bryson-Richardson, D. Logan, 2004, Gene.

Melanocortin 1 receptor variation in the domestic dog

G. Barsh, I. Jackson, J. Newton, 2000, Mammalian Genome.

Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation

I. Jackson, M. Fukata, Y. Fukata, 2009, PLoS genetics.

Molecular and developmental genetics of mouse coat color.

I. Jackson, Ian J. Jackson, 1994, Annual review of genetics.

Functional Annotation of Mouse Genome Sequences

Hans Lehrach, William C. Skarnes, Wolfgang Wurst, 2001, Science.

Molecular characterization of a human tyrosinase-related-protein-2 cDNA

I. Jackson, 2004 .

Homologous pigmentation mutations in human, mouse and other model organisms.

I. Jackson, Ian J. Jackson, 1997, Human molecular genetics.

Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair

I. Jackson, E. Healy, J. Rees, 2000, The Lancet.

Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation.

I. Jackson, N. Flanagan, E. Healy, 2000, Human molecular genetics.

A cell/cilia cycle biosensor for single cell kinetics reveals persistence of cilia after the G1/ S transition is a general property in cells and mice

A. Miyawaki, Asako Sakaue-Sawano, I. Jackson, 2022 .

Explorer Spinster Homolog 2 ( Spns 2 ) Deficiency Causes Early Onset Progressive Hearing Loss

Jacqueline K. White, K. Steel, D. Jagger, 2017 .

Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss

Jacqueline K. White, K. Steel, D. Jagger, 2014, PLoS genetics.

Structure of the mouse tyrosinase-related protein-2/dopachrome tautomerase (Tyrp2/Dct) gene and sequence of two novel slaty alleles.

I. Jackson, P. Budd, Ian J. Jackson, 1995, Genomics.

Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse.

I. Jackson, B. Kwon, E. Rinchik, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Regulation of pigmentation in zebrafish melanophores.

I. Jackson, D. Logan, S. Burn, 2006, Pigment cell research.

mc1r Pathway regulation of zebrafish melanosome dispersion.

I. Jackson, D. Porteous, P. Lundegaard, 2008, Zebrafish.

Explorer A zebrafish model for nevus regeneration

C. Ceol, I. Jackson, E. Patton, 2017 .

A zebrafish model for nevus regeneration

C. Ceol, I. Jackson, E. Patton, 2011, Pigment cell & melanoma research.

A second tyrosinase‐related protein, TRP‐2, is a melanogenic enzyme termed DOPAchrome tautomerase.

I. Jackson, K. Urabe, V. Hearing, 1992, The EMBO journal.

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

I. Jackson, S. Shirran, C. Botting, 2014, Molecular biology of the cell.

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

S. Cross, S. Wells, I. Jackson, 2020, Scientific Reports.

PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins

Mark T. Handley, I. Jackson, R. Ribchester, 2017, American journal of human genetics.

The mouse Cer1 (Cerberus related or homologue) gene is not required for anterior pattern formation.

I. Jackson, Dabney K. Johnson, P. Hunsicker, 1999, Developmental biology.

Investigating the genetic architecture of eye colour in a Canadian cohort

Michael A. Kovacs, K. Brown, I. Jackson, 2021, bioRxiv.

A late wave of melanoblast differentiation and rostrocaudal migration revealed in patch and rump-white embryos

I. Jackson, S. Jordan, 2000, Mechanisms of Development.

Getting under the skin

I. Jackson, 2007, Nature Medicine.

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

Thomas M. Keane, Wei-yuan, R. Durbin, 2017 .

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

S. Cross, I. Jackson, U. Schlötzer-Schrehardt, 2005, Human molecular genetics.

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

I. Jackson, U. Schlötzer-Schrehardt, J. Mullins, 2010, Human molecular genetics.

Edinburgh Research Explorer Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

S. Cross, S. Greenaway, A. Mallon, 2016 .

Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep

I. Jackson, P. Nolan, S. Peirson, 2015, Neurobiology of Aging.

The G-netics of dark skin

I. Jackson, 2004, Nature Genetics.

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

I. Jackson, P. Coffey, C. Thaung, 2002, Neuroscience Letters.

A Novel Mouse Model of Warburg Micro Syndrome Reveals Roles for RAB18 in Eye Development and Organisation of the Neuronal Cytoskeleton Running title: Pathology of WARBM in RAB18 mice

Mark T. Handley, I. Jackson, Harris Morrison, 2014 .

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

Mark T. Handley, I. Jackson, Harris Morrison, 2014, Disease Models & Mechanisms.

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

S. Wells, I. Jackson, P. Potter, 2013, Investigative ophthalmology & visual science.

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

I. Jackson, M. Perretti, D. Davidson, 2010 .

Human β-defensin 3 has immunosuppressive activity in vitro and in vivo

I. Jackson, M. Perretti, D. Davidson, 2010, European Journal of Immunology.

The cloning and sequencing of a cDNA coding for chick tyrosinase-related protein-1.

I. Jackson, S. Kidson, C. S. April, 1998, Biochimica et biophysica acta.

The mahogany mouse mutation: further links between pigmentation, obesity and the immune system.

I. Jackson, 1999, Trends in genetics : TIG.

Melanocortin receptors and antagonists regulate pigmentation and body weight.

I. Jackson, S. Jordan, 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.

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

Martin A. M. Reijns, P. Lockhart, I. Jackson, 2011, American journal of human genetics.

UvA-DARE ( Digital Academic Repository ) Loss of the BMP Antagonist , SMOC-1 , Causes Ophthalmo-Acromelic ( Waardenburg Anophthalmia ) Syndrome in Humans and Mice

Wieczorek, Dagmar, Rosanna, 2011 .

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse.

S. Cross, I. Jackson, L. Sánchez-Pulido, 2019, Investigative ophthalmology & visual science.

MGF (KIT ligand) is a chemokinetic factor for melanoblast migration into hair follicles.

I. Jackson, S. Jordan, Siobhán A. Jordan, 2000, Developmental biology.

Identification of the albino mutation of mouse tyrosinase by analysis of an in vitro revertant.

I. Jackson, D. Bennett, Dot C Bennett, 1990, Proceedings of the National Academy of Sciences of the United States of America.

The absence of introns within a human fibroblast interferon gene.

I. Jackson, A. Porter, S. Doel, 1981, Nucleic acids research.

Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse

I. Jackson, D. Adams, D. Fitzpatrick, 2022, bioRxiv.

TRP-2 | DT , a new early melanoblast marker , shows that steel survival factor 1111 growth factor ( c-kit ligand ) is a

D. Davidson, I. Jackson, Karen P. Steeli, 2010 .

Deficiency of Trp53 rescues the male fertility defects of Kit(W-v) mice but has no effect on the survival of melanocytes and mast cells.

I. Jackson, R. Speed, S. Jordan, 1999, Developmental biology.

Deficiency of Trp 53 Rescues the Male Fertility Defects of KitW-v Mice but Has No Effect on he Survival of Melanocytes and Mast Cells

I. Jackson, R. Speed, S. Jordan, 1999 .

β-Defensin Repertoire Expands

I. Jackson, J. Dorin, 2007, Science.

White-based brown (Tyrp1B-w) is a dominant mutation causing reduced hair pigmentation owing to a chromosomal inversion

I. Jackson, S. Javerzat, 1998, Mammalian Genome.

Maintenance of distinct melanocyte populations in the interfollicular epidermis

I. Jackson, D. Headon, R. Mort, 2015, Pigment cell & melanoma research.

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

S. Cross, I. Jackson, J. Morgan, 2004, Human molecular genetics.

Explorer A novel mouse model of Warburg Micro Syndrome reveals roles for RAB 18 in eye development and organisation of the neuronal cytoskeleton

Mark T. Handley, I. Jackson, Harris Morrison, 2016 .

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

I. Jackson, M. Fisher, D. Fitzpatrick, 2013, PLoS genetics.

Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

I. Jackson, R. Hennekam, H. Brunner, 2011, PLoS genetics.

Genetics and molecular biology of mouse pigmentation.

K. Steel, I. Jackson, P. Budd, 1994, Pigment cell research.

Haploinsufficiency for Phox 2 b in mice causes dilated pupils and atrophy of the ciliary ganglion : mechanistic insights into human congenital central hypoventilation syndrome

S. Cross, I. Jackson, J. Morgan, 2004 .

Assignment of the TIMP gene to the murine X-chromosome using an inter-species cross.

I. Jackson, A. Docherty, T. LeCras, 1987, Nucleic acids research.

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

Martin S. Taylor, I. Jackson, I. Smyth, 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

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.

I. Jackson, I. Jackson, J. Friedman, 1994, Genetics.

Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.

Jacqueline K. White, S. Cross, I. Jackson, 2015, Investigative ophthalmology & visual science.

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4.

I. Jackson, S. Povey, C. Abbott, 1991, Genomics.

Gametogenesis and the Early Embryo

I. Jackson, 1988 .

Skin type, melanoma, and melanocortin 1 receptor variants.

I. Jackson, E. Healy, J. Rees, 1999, The Journal of investigative dermatology.

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

S. Nishikawa, I. Jackson, Y. Barrandon, 2002, Nature.

Explorer Acute Versus Chronic Loss of Mammalian Azi 1 / Cep 131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2017 .

Acute Versus Chronic Loss of Mammalian Azi1/Cep131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2013, PLoS genetics.

Explorer The melanocyte lineage in development and disease

I. Jackson, E. Patton, R. Mort, 2017 .

The melanocyte lineage in development and disease

Richard L. Mort, I. Jackson, E. Patton, 2015, Development.

A mouse model of brittle cornea syndrome caused by mutation in Zfp469

I. Jackson, V. Vitart, Chloe M. Stanton, 2021, bioRxiv.

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

Steve D. M. Brown, S. Cross, I. Jackson, 2002, Human molecular genetics.

Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

S. Ring, I. Jackson, R. Hennekam, 2012, The Journal of investigative dermatology.

Functional properties of cloned melanogenic proteins.

I. Jackson, K. Urabe, V. Hearing, 1992, Pigment cell research.

A cDNA encoding tyrosinase-related protein maps to the brown locus in mouse.

I. Jackson, Ian J. Jackson, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Molecular characterization of a human tyrosinase-related-protein-2 cDNA. Patterns of expression in melanocytic cells.

I. Jackson, L. Dubertret, V. del Marmol, 1994, European journal of biochemistry.

Peroxidase activity in the ink gland of Sepia officinalis and partial nucleotide sequence of a candidate cDNA encoding the enzyme.

I. Jackson, A. Palumbo, 1995 .

TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor.

K. Steel, D. Davidson, I. Jackson, 1992, Development.

Dopachrome tautomerase variants in patients with oculocutaneous albinism

I. Jackson, P. Pennamen, D. Lacombe, 2020, Genetics in Medicine.

Variants of the melanocyte–stimulating hormone receptor gene are associated with red hair and fair skin in humans

Ian Jackson, I. Jackson, E. Healy, 1995, Nature Genetics.

Melanocortin 1 receptor variants in an Irish population.

I. Jackson, N. Flanagan, E. Healy, 1998, The Journal of investigative dermatology.

Mouse coat colour mutations: A molecular genetic resource which spans the centuries

I. Jackson, 1991, BioEssays : news and reviews in molecular, cellular and developmental biology.

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

Zhiqiang Zeng, R. Kelsh, J. Lister, 2011, Development.

Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability

K. Rawlik, I. Jackson, A. Tenesa, 2018, Nature Communications.

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

Niels Morling, I. Jackson, N. Morling, 2009, BMC Genetics.

Bcl2 Regulation by the Melanocyte Master Regulator Mitf Modulates Lineage Survival and Melanoma Cell Viability

Sridhar Ramaswamy, Todd R. Golub, David E. Fisher, 2002, Cell.

Characterization of TRP-1 mRNA levels in dominant and recessive mutations at the mouse brown (b) locus.

I. Jackson, D. Bennett, E. Rinchik, 1990, Genetics.

Investigating the genetic architecture of eye colour in a Canadian cohort

Michael A. Kovacs, K. Brown, I. Jackson, 2021, bioRxiv.

The retinal pigmented epithelium is required for development and maintenance of the mouse neural retina

I. Jackson, S. Raymond, 1995, Current Biology.

DEVELOPMENTAL GENETICS OF MOUSE COAT COLOR

I. Jackson, 1994 .

Light is a dominant mouse mutation resulting in premature cell death

I. Jackson, R. Johnson, Jackson Ij, 1992, Nature Genetics.

HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus

D. Bonthron, I. Jackson, A. von Kriegsheim, 2014, PLoS genetics.

The melanocyte lineage in development and disease

Richard L. Mort, I. Jackson, E. Patton, 2015, Development.

Evolution and expression of tyrosinase-related proteins.

I. Jackson, 1994, Pigment cell research.

The Dct−/− Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism

E. Gontier, I. Jackson, S. Javerzat, 2022, bioRxiv.

The molecular basis of brown, an old mouse mutation, and of an induced revertant to wild type.

I. Jackson, J. Favor, E. Žďárský, 1990, Genetics.

Mutations at the W locus affect survival of neural crest-derived melanocytes in the mouse

K. Steel, I. Jackson, J. Cable, 1995, Mechanisms of Development.

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma.

I. Jackson, A. Carothers, E. Healy, 1996, Human molecular genetics.

Cell signalling: Red alert about lipid's role in skin cancer

I. Jackson, E. Patton, 2017, Nature.

Functional variation of MC1R alleles from red-haired individuals.

I. Jackson, E. Healy, J. Rees, 2001, Human molecular genetics.

Humanized MC1R transgenic mice reveal human specific receptor function.

I. Jackson, M. Keighren, P. Budd, 2007, Human molecular genetics.

Activation of the receptor tyrosine kinase Kit is required for the proliferation of melanoblasts in the mouse embryo.

I. Jackson, S. Jordan, P. Budd, 1997, Developmental biology.

More to colour than meets the eye

I. Jackson, 1993, Current Biology.

The genetic architecture of hair colour in the UK population

K. Rawlik, I. Jackson, A. Tenesa, 2018, bioRxiv.

Genetics and biology of mouse melanocytes: Mutation, migration and interaction

I. Jackson, 1985 .

Light (Blt), a mutation that causes melanocyte death, affects stria vascularis function in the mouse inner ear.

K. Steel, I. Jackson, J. Cable, 1993, Pigment cell research.

Ex vivo live imaging of melanoblast migration in embryonic mouse skin

I. Jackson, R. Mort, Leonard Hay, 2010, Pigment cell & melanoma research.

A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus

D. Watkins-Chow, W. Pavan, I. Jackson, 2021, Human mutation.

The tyrosinase-related protein-1 gene has a structure and promoter sequence very different from tyrosinase.

I. Jackson, P. Budd, R. Johnson, 1991, Nucleic acids research.

Genetic and environmental factors modify bovine spongiform encephalopathy incubation period in mice

I. Jackson, I. Mcconnell, J. Manson, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Evidence for variable selective pressures at MC1R.

I. Jackson, A. Sajantila, R. Harding, 2000, American journal of human genetics.

Towards high resolution maps of the mouse and human genomes--a facility for ordering markers to 0.1 cM resolution. European Backcross Collaborative Group.

D. Simon, A. Ashworth, S. Rastan, 1994, Human molecular genetics.

Developmental programming: Prenatal testosterone excess disrupts pancreatic islet developmental trajectory in female sheep

I. Jackson, V. Padmanabhan, A. Veiga-Lopez, 2020, Molecular and Cellular Endocrinology.

Signatures of Diversifying Selection in European Pig Breeds

I. Jackson, M. Groenen, R. Crooijmans, 2013, PLoS genetics.

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

Jennifer P Morton, Paul Timpson, Richard L Mort, 2011, Nature communications.

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

I. Jackson, J. Dukes-McEwan, 2002, Mammalian Genome.

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification

S. Cross, I. Jackson, T. Hurd, 2019, bioRxiv.

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

I. Jackson, S. Snapper, O. Sansom, 2011, Developmental cell.

DEV123729 1387..1387

I. Jackson, E. Patton, R. Mort, 2015 .

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

Steve D. M. Brown, S. Cross, S. Greenaway, 2016, Nature Communications.

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

I. Jackson, A. L. Wilkie, S. Jordan, 2002, Development.

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

S. Cross, I. Jackson, T. Webb, 2008, Journal of Cell Science.

A Conditional Zebrafish MITF Mutation Reveals MITF Levels Are Critical for Melanoma Promotion vs. Regression In Vivo

J. Lister, I. Jackson, E. Patton, 2013, The Journal of investigative dermatology.

A reappraisal of non-consensus mRNA splice sites.

I. Jackson, I J Jackson, 1991, Nucleic acids research.

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

Henrik Westerberg, John M. Hancock, Steve D. M. Brown, 2013, Genome Biology.

Expanded Analysis of Pigmentation Genetics in UK Biobank

K. Rawlik, K. Brown, W. Pavan, 2022, bioRxiv.

Phenotypic rescue of mutant brown melanocytes by a retrovirus carrying a wild-type tyrosinase-related protein gene.

R. Jaenisch, I. Jackson, P. Laipis, 1990, Development.

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

Steve D. M. Brown, S. Cross, I. Jackson, 2010, Human molecular genetics.

Domains of the positive transcription factor specific for the Xenopus 5S RNA gene

I. Jackson, Douglas R. Smith, Donald D. Brown, 1984, Cell.

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

I. Jackson, M. Keighren, Hiroaki Yamamoto, 2006, Pigment cell research.

Genomic anatomy of the Tyrp1 (brown) deletion complex.

Jane Loveland, Jonathan M. Mudge, Jennifer Harrow, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Characterisation of two identical independent non-homologous integration sites in mouse embryonic stem cells.

R. Lovell-Badge, I. Jackson, H. Sutherland, 1993, Gene.

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

S. Cross, I. Jackson, D. Threadgill, 2004, Mammalian Genome.

Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs

Martin S. Taylor, P. Scambler, I. Jackson, 2005, Nature Genetics.

Mutation Spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and Genotype–Phenotype Correlations in Warburg Micro Syndrome and Martsolf Syndrome

Mark T. Handley, I. Jackson, I. Glass, 2013, Human mutation.

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

Henrik Westerberg, John M. Hancock, Steve D. M. Brown, 2013, Genome Biology.

Explorer HEATR 2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus

Amaya Garcia Munoz, D. Bonthron, I. Jackson, 2017 .

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

Martin S. Taylor, Monica J Justice, Ian Smyth, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Divergent selection experiments: a powerful tool for unravelling the genetic regulation of complex traits.

K. Rawlik, I. Jackson, J. Prendergast, 2018 .

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

S. Cross, I. Jackson, Richard S. Smith, 2014, PLoS Genetics.

Molecular cloning and sequence analysis of a chicken cDNA encoding tyrosinase-related protein-2/DOPAchrome tautomerase.

I. Jackson, S. Kidson, C. S. April, 1998, Gene.

A mouse homoeo box gene is expressed during embryogenesis and in adult kidney

I. Jackson, P. Schofield, B. Hogan, 1985, Nature.

Explorer Pleiotropic effects of the melanocortin 1 receptor ( MC 1 R ) gene on human pigmentation

I. Jackson, N. Flanagan, E. Healy, 2018 .

Explorer The Asp 84 Glu variant of the melanocortin 1 receptor ( MC 1 R ) is associated with melanoma

I. Jackson, A. Carothers, J. Rees, 2015 .

Evolution in action: highlighting a role for the Agouti gene in development?

I. Jackson, 2011 .

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

I. Jackson, 2013, Pigment cell & melanoma research.

Sequence Characterization of Teleost Fish Melanocortin Receptors

Martin S. Taylor, I. Jackson, R. Bryson-Richardson, 2003, Annals of the New York Academy of Sciences.

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

Martin S. Taylor, I. Jackson, R. Bryson-Richardson, 2003, Genomics.

The developmental expression of the gene for TFIIIA in Xenopus laevis.

I. Jackson, A. Kumar, D. D. Brown, 1986, Nucleic Acids Research.

KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability

I. Jackson, A. von Kriegsheim, N. Gilbert, 2017, The Journal of cell biology.

Mouse genomics: Making sense of the sequence

I. Jackson, 2001, Current Biology.

Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome

Martin S. Taylor, Mark T. Handley, I. Jackson, 2014, Molecular genetics & genomic medicine.

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

I. Jackson, J. Rees, T. H. Wong, 2010, Experimental dermatology.

Rac 1 drives melanoblast organization during mouse development by orchestrating pseudopod-driven motility and cell-cycle progression

I. Jackson, S. Snapper, O. Sansom, 2012 .

No Mickey Mouse genetics.

I. Jackson, 1988, Trends in genetics : TIG.

The murine Hox-2 cluster of homeo box containing genes maps distal on chromosome 11 near the tail-short (Ts) locus.

D. Cox, I. Jackson, B. Hogan, 1986, Cytogenetics and cell genetics.

Edinburgh Research Explorer A zebrafish model for nevus regeneration

C. Ceol, I. Jackson, E. Patton, 2011 .

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

S. Cross, I. Jackson, L. Sánchez-Pulido, 2019, bioRxiv.

Identification, sequence, and mapping of the mouse multiple PDZ domain protein gene, Mpdz.

I. Jackson, E. H. Simpson, R. Suffolk, 1999, Genomics.

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

S. Cross, I. Jackson, S. Bhattacharya, 2006, Human molecular genetics.

A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23

M. Justice, I. Jackson, Dabney K. Johnson, 2000, Mammalian Genome.

Genetic background modifies vulnerability to glaucoma-related phenotypes in Lmx1b mutant mice

S. Cross, I. Jackson, S. John, 2020, Disease Models & Mechanisms.

Explorer Loss of ALDH 18 A 1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3 A and Warburg Micro syndrome

Martin S. Taylor, Mark T. Handley, I. Jackson, 2017 .

Involvement of the Melanocortin-1 Receptor in Acute Pain and Pain of Inflammatory but Not Neuropathic Origin

I. Jackson, S. Fleetwood-Walker, A. Delaney, 2010, PloS one.

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

S. Cross, I. Jackson, Richard S. Smith, 2014, PLoS genetics.

Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model

Ruth E. Baker, Christian A. Yates, Gabriel Landini, 2016, Nature Communications.

Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation

Mark T. Handley, I. Jackson, D. Fitzpatrick, 2015, Open Biology.

Ex vivo culture of mouse embryonic skin and live-imaging of melanoblast migration.

I. Jackson, R. Mort, M. Keighren, 2014, Journal of visualized experiments : JoVE.

Fucci2a: A bicistronic cell cycle reporter that allows Cre mediated tissue specific expression in mice

Atsushi Miyawaki, Asako Sakaue-Sawano, Peter Hohenstein, 2014, Cell cycle.

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

J. Forrester, I. Jackson, C. McCaig, 2010, Neuropharmacology.

Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical 1 model 2 3

Robert J. H. Ross, I. Jackson, K. Painter, 2016 .

12th International Mouse Genome Conference.

S. Cross, I. Jackson, K. Manolakou, 1999, Genomics.

Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2‐mediated recombination in the melanocyte lineage

Emma L. Wilkinson, I. Jackson, S. Allinson, 2022, Pigment cell & melanoma research.

Fucci 2 a : A bicistronic cell cycle reporter that allows Cre mediated tissue speci fi c expression in mice

A. Miyawaki, Asako Sakaue-Sawano, I. Jackson, 2014 .

Genotype – Phenotype Correlation of Mouse Pde 6 b Mutations

S. Cross, I. Jackson, J. Morgan, 2005 .

Production of mouse Hox-2.1 protein in Escherichia coli: characterisation of in vitro binding to DNA.

I. Jackson, P. Budd, 1991, Gene.

A high-resolution map of the brown (b, Tyrp1) deletion complex of mouse Chromosome 4

I. Jackson, E. Rinchik, R. Suffolk, 1995, Mammalian Genome.

Genotype-phenotype correlation of mouse pde6b mutations.

S. Cross, I. Jackson, J. Morgan, 2005, Investigative ophthalmology & visual science.

Mapping in the region of Danforth's short tail and the localization of tail length modifiers.

I. Jackson, B. Taylor, C. Abbott, 1997, Genome research.

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

I. Jackson, J. Sharpe, D. Price, 2004, Developmental biology.

Evidence for variable selective pressures at MC1R.

I. Jackson, R. Harding, N. Flanagan, 2000, American journal of human genetics.

A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice

Asako Sakaue-Sawano, I. Jackson, R. Meehan, 2018, Developmental cell.

Pigmentary Diversity: Identifying the genes causing human diversity

I. Jackson, 2006, European Journal of Human Genetics.

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function

S. Cross, I. Jackson, J. Marsh, 2018, Disease Models & Mechanisms.

Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

I. Jackson, R. Hennekam, H. Brunner, 2018, PLoS Genetics.

Human β‐defensin 3 has immunosuppressive activity in vitro and in vivo

I. Jackson, M. Perretti, D. Davidson, 2010 .

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

I. Jackson, J. Norman, C. Der, 2011, Nature communications.

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

I. Jackson, M. Fisher, D. Keene, 2013, PLoS genetics.

Mouse genetics and transgenics : a practical approach

I. Jackson, C. Abbott, 2000 .

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

I. Jackson, S. Snapper, O. Sansom, 2011, Developmental cell.

Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation

I. Jackson, M. Fukata, Y. Fukata, 2009, PLoS genetics.

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

Martin A. M. Reijns, P. Lockhart, I. Jackson, 2011, American journal of human genetics.

The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells

S. Cross, I. Jackson, G. Nicholson, 2015, Disease Models & Mechanisms.

The molecular basis of brown, an old mouse mutation, and of an induced revertant to wild type.

I. Jackson, J. Favor, E. Z̆dárský, 1990, Genetics.

Newcastle University Eprints Date Deposited: 3 This Work Is Licensed under a Creative Commons Attribution 4.0 International License Acute versus Chronic Loss of Mammalian Azi1/cep131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2022 .