Works by Jackson, Ian J.
Results: 60
Expression of the fras1/frem gene family during zebrafish development and fin morphogenesis.
- Published in:
- Developmental Dynamics, 2008, v. 237, n. 11, p. 3295, doi. 10.1002/dvdy.21729
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- Article
A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus.
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- Human Mutation, 2021, v. 42, n. 10, p. 1239, doi. 10.1002/humu.24257
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- Article
Do mammals need P elements?
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- Nature, 1986, v. 321, n. 6071, p. 656, doi. 10.1038/321656a0
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- Article
A mouse homoeo box gene is expressed during embryogenesis and in adult kidney.
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- Nature, 1985, v. 317, n. 6039, p. 745, doi. 10.1038/317745a0
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- Article
Molecular biology: Transposable elements and suppressor genes.
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- Nature, 1984, v. 309, n. 5971, p. 751, doi. 10.1038/309751b0
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- Article
The physiological and phenotypic determinants of human tanning measured as change in skin colour following a single dose of ultraviolet B radiation.
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- Experimental Dermatology, 2010, v. 19, n. 7, p. 667, doi. 10.1111/j.1600-0625.2010.01078.x
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- Article
Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2‐mediated recombination in the melanocyte lineage.
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- Pigment Cell & Melanoma Research, 2023, v. 36, n. 1, p. 71, doi. 10.1111/pcmr.13076
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- Article
Maintenance of distinct melanocyte populations in the interfollicular epidermis.
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- Pigment Cell & Melanoma Research, 2015, v. 28, n. 4, p. 476, doi. 10.1111/pcmr.12375
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- Article
How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns.
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- Pigment Cell & Melanoma Research, 2013, v. 26, n. 4, p. 438, doi. 10.1111/pcmr.12101
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- Article
A zebrafish model for nevus regeneration.
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- Pigment Cell & Melanoma Research, 2011, v. 24, n. 2, p. 378, doi. 10.1111/j.1755-148X.2011.00839.x
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- Article
In praise of books.
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- 2011
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- Book Review
Ex vivo live imaging of melanoblast migration in embryonic mouse skin.
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- 2010
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- Publication type:
- Letter
KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability.
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- Journal of Cell Biology, 2017, v. 216, n. 4, p. 999, doi. 10.1083/jcb.201607032
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- Article
The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype.
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- Human Molecular Genetics, 2011, v. 20, n. 2, p. 223, doi. 10.1093/hmg/ddq457
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- Publication type:
- Article
Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume.
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- Human Molecular Genetics, 2010, v. 19, n. 6, p. 1119, doi. 10.1093/hmg/ddp584
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- Article
Humanized MC1R transgenic mice reveal human specific receptor function.
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- Human Molecular Genetics, 2007, v. 16, n. 19, p. 2341, doi. 10.1093/hmg/ddm191
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- Article
Cardiac malformations and midline skeletal defects in mice lacking filamin A.
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- Human Molecular Genetics, 2006, v. 15, n. 16, p. 2457, doi. 10.1093/hmg/ddl168
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- Publication type:
- Article
Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy.
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- Human Molecular Genetics, 2005, v. 14, n. 21, p. 3161, doi. 10.1093/hmg/ddi348
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- Article
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.
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- Human Molecular Genetics, 2004, v. 13, n. 14, p. 1433, doi. 10.1093/hmg/ddh156
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- Article
Novel ENU-induced eye mutations in the mouse: models for human eye disease.
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- Human Molecular Genetics, 2002, v. 11, n. 7, p. 755, doi. 10.1093/hmg/11.7.755
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- Article
Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse.
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- Genes, 2022, v. 13, n. 10, p. N.PAG, doi. 10.3390/genes13101797
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- Article
The Dct −/− Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism.
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- Genes, 2022, v. 13, n. 7, p. 1164, doi. 10.3390/genes13071164
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- Article
Colour-coded switches.
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- Nature, 1993, v. 362, n. 6421, p. 587, doi. 10.1038/362587a0
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- Article
Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model.
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- Nature Communications, 2016, v. 7, n. 1, p. 10288, doi. 10.1038/ncomms10288
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- Publication type:
- Article
A Conditional Zebrafish MITF Mutation Reveals MITF Levels Are Critical for Melanoma Promotion vs. Regression In Vivo.
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- Journal of Investigative Dermatology, 2014, v. 134, n. 1, p. 133, doi. 10.1038/jid.2013.293
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- Publication type:
- Article
Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development.
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- Journal of Investigative Dermatology, 2012, v. 132, n. 8, p. 2026, doi. 10.1038/jid.2012.95
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- Article
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.
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- Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 4, p. 319, doi. 10.1002/mgg3.70
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- Article
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07691-z
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- Article
Pigmentary Diversity: Identifying the genes causing human diversity.
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- European Journal of Human Genetics, 2006, v. 14, n. 9, p. 978, doi. 10.1038/sj.ejhg.5201659
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- Article
Skin Type, Melanoma, and Melanocortin 1 Receptor Variants.
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- Journal of Investigative Dermatology, 1999, v. 112, n. 4, p. 512, doi. 10.1046/j.1523-1747.1999.00554.x
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- Article
Melanocortin 1 Receptor Variants in an Irish Population.
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- Journal of Investigative Dermatology, 1998, v. 111, n. 1, p. 119, doi. 10.1046/j.1523-1747.1998.00252.x
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- Article
Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss.
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- PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004688
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- Article
HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus.
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- PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004577
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- Article
A Dominant-Negative Mutation of Mouse <i>Lmx1b</i> Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation.
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- PLoS Genetics, 2014, v. 10, n. 5, p. 1, doi. 10.1371/journal.pgen.1004359
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- Article
A <i>Trans</i>-Acting Protein Effect Causes Severe Eye Malformation in the <i>Mp</i> Mouse.
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- PLoS Genetics, 2013, v. 9, n. 12, p. 1, doi. 10.1371/journal.pgen.1003998
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- Article
Acute Versus Chronic Loss of Mammalian <i>Azi1/Cep131</i> Results in Distinct Ciliary Phenotypes.
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- PLoS Genetics, 2013, v. 9, n. 12, p. 1, doi. 10.1371/journal.pgen.1003928
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- Article
Signatures of Diversifying Selection in European Pig Breeds.
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- PLoS Genetics, 2013, v. 9, n. 4, p. 1, doi. 10.1371/journal.pgen.1003453
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- Article
Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation.
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- PLoS Genetics, 2009, v. 5, n. 11, p. 1, doi. 10.1371/journal.pgen.1000748
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- Article
Characterization of TRP-1 mRNA Levels in Dominant and Recessive Mutations at the Mouse brown (b) Locus.
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- Genetics, 1990, v. 126, n. 2, p. 451
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- Article
The Molecular Basis of brown, an Old Mouse Mutation, and of an Induced Revertant to Wild Type.
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- Genetics, 1990, v. 126, n. 2, p. 443
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- Article
Functional variation of MC1Ralleles from red-haired individuals.
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- Human Molecular Genetics, 2001, v. 10, n. 21, p. 2397, doi. 10.1093/hmg/10.21.2397
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- Article
Homologous Pigmentation Mutations in Human, Mouse and Other Model Organisms.
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- Human Molecular Genetics, 1997, v. 6, n. 10, p. 1613, doi. 10.1093/hmg/6.10.1613
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- Article
The Asp84Glu Variant of the Melanocortin 1 Receptor (MC1R) is Associated with Melanoma.
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- Human Molecular Genetics, 1996, v. 5, n. 10, p. 1663, doi. 10.1093/hmg/5.10.1663
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- Publication type:
- Article
Sequence Characterization of Teleost Fish Melanocortin Receptors.
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- Annals of the New York Academy of Sciences, 2003, v. 994, n. 1, p. 319, doi. 10.1111/j.1749-6632.2003.tb03196.x
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- Publication type:
- Article
Getting under the skin.
- Published in:
- 2007
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- Publication type:
- Book Review
The G-netics of dark skin.
- Published in:
- Nature Genetics, 2004, v. 36, n. 9, p. 935, doi. 10.1038/ng0904-935
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- Article
Mouse mutagenesis on target.
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- Nature Genetics, 2001, v. 28, n. 3, p. 198, doi. 10.1038/90017
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- Publication type:
- Article
The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification.
- Published in:
- PLoS Genetics, 2020, v. 16, n. 4, p. 1, doi. 10.1371/journal.pgen.1008583
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- Publication type:
- Article
Melanocortin receptors and antagonists regulate pigmentation and body weight.
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- BioEssays, 1998, v. 20, n. 8, p. 603, doi. 10.1002/(SICI)1521-1878(199808)20:8<603::AID-BIES1>3.0.CO;2-J
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- Publication type:
- Article
Mouse coat colour mutations: A molecular genetic resource which spans the centuries.
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- BioEssays, 1991, v. 13, n. 9, p. 439, doi. 10.1002/bies.950130903
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- Publication type:
- Article