Ex vivo live imaging of melanoblast migration in embryonic mouse skin

por Mort, Richard L, Hay, Leonard, Jackson, Ian J
Publicado 2010

The melanocyte lineage in development and disease

por Mort, Richard L., Jackson, Ian J., Patton, E. Elizabeth
Publicado 2015

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

por Delaney, Ada, Keighren, Margaret, Fleetwood-Walker, Susan M., Jackson, Ian J.
Publicado 2010

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

por Mengel-From, Jonas, Wong, Terence H, Morling, Niels, Rees, Jonathan L, Jackson, Ian J
Publicado 2009

A zebrafish model for nevus regeneration

por Richardson, Jennifer, Zeng, Zhiqiang, Ceol, Craig, Mione, Marina, Jackson, Ian J, Patton, E Elizabeth
Publicado 2011

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

por Handley, Mark T, Mégarbané, André, Meynert, Alison M, Brown, Stephen, Freyer, Elisabeth, Taylor, Martin S, Jackson, Ian J, Aligianis, Irene A
Publicado 2014

Maintenance of distinct melanocyte populations in the interfollicular epidermis

por Glover, James D., Knolle, Stefan, Wells, Kirsty L., Liu, Dianbo, Jackson, Ian J., Mort, Richard L., Headon, Denis J.
Publicado 2015

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

por Lister, James A, Capper, Amy, Zeng, Zhiqiang, Mathers, Marie E, Richardson, Jennifer, Paranthaman, Karthika, Jackson, Ian J, Patton, E Elizabeth
Publicado 2014

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

por Morgan, Michael D., Pairo-Castineira, Erola, Rawlik, Konrad, Canela-Xandri, Oriol, Rees, Jonathan, Sims, David, Tenesa, Albert, Jackson, Ian J.
Publicado 2018

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

por Stanton, Chloe M., Findlay, Amy S., Drake, Camilla, Mustafa, Mohammad Z., Gautier, Philippe, McKie, Lisa, Jackson, Ian J., Vitart, Veronique
Publicado 2021

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

por Hall, Emma A., Keighren, Margaret, Ford, Matthew J., Davey, Tracey, Jarman, Andrew P., Smith, Lee B., Jackson, Ian J., Mill, Pleasantine
Publicado 2013

Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation

por Handley, Mark T., Carpanini, Sarah M., Mali, Girish R., Sidjanin, Duska J., Aligianis, Irene A., Jackson, Ian J., FitzPatrick, David R.
Publicado 2015

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

por Findlay, Amy S., McKie, Lisa, Keighren, Margaret, Clementson-Mobbs, Sharon, Sanchez-Pulido, Luis, Wells, Sara, Cross, Sally H., Jackson, Ian J.
Publicado 2020

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

por Cross, Sally H., McKie, Lisa, West, Katrine, Coghill, Emma L., Favor, Jack, Bhattacharya, Shoumo, Brown, Steve D.M., Jackson, Ian J.
Publicado 2011

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

por Semple, Fiona, Webb, Sheila, Li, Hsin-Ni, Patel, Hetal B, Perretti, Mauro, Jackson, Ian J, Gray, Mohini, Davidson, Donald J, Dorin, Julia R
Publicado 2010

Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation

por Mill, Pleasantine, Lee, Angela W. S., Fukata, Yuko, Tsutsumi, Ryouhei, Fukata, Masaki, Keighren, Margaret, Porter, Rebecca M., McKie, Lisa, Smyth, Ian, Jackson, Ian J.
Publicado 2009

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

por Banks, Gareth, Heise, Ines, Starbuck, Becky, Osborne, Tamzin, Wisby, Laura, Potter, Paul, Jackson, Ian J., Foster, Russell G., Peirson, Stuart N., Nolan, Patrick M.
Publicado 2015

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

por Parker, Andrew, Cross, Sally H., Jackson, Ian J., Hardisty-Hughes, Rachel, Morse, Susan, Nicholson, George, Coghill, Emma, Bowl, Michael R., Brown, Steve D. M.
Publicado 2015

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

por Cross, Sally H., Mckie, Lisa, Hurd, Toby W., Riley, Sam, Wills, Jimi, Barnard, Alun R., Young, Fiona, MacLaren, Robert E., Jackson, Ian J.
Publicado 2020

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

por Tingaud-Sequeira, Angèle, Mercier, Elina, Michaud, Vincent, Pinson, Benoît, Gazova, Ivet, Gontier, Etienne, Decoeur, Fanny, McKie, Lisa, Jackson, Ian J., Arveiler, Benoît, Javerzat, Sophie
Publicado 2022