Gametogenesis and the Early Embryo

Por Jackson, Ian J
Publicado em 1988

Ex vivo live imaging of melanoblast migration in embryonic mouse skin

Por Mort, Richard L, Hay, Leonard, Jackson, Ian J
Publicado em 2010

The melanocyte lineage in development and disease

Por Mort, Richard L., Jackson, Ian J., Patton, E. Elizabeth
Publicado no Development (2015)

The melanocyte lineage in development and disease

Por Mort, Richard L., Jackson, Ian J., Patton, E. Elizabeth
Publicado no Development (2015)

Ex vivo Culture of Mouse Embryonic Skin and Live-imaging of Melanoblast Migration

Por Mort, Richard L., Keighren, Margaret, Hay, Leonard, Jackson, Ian J.
Publicado em 2014

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 em 2010

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

Por Smyth, Ian, Du, Xin, Taylor, Martin S., Justice, Monica J., Beutler, Bruce, Jackson, Ian J.
Publicado em 2004

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 em 2009

A zebrafish model for nevus regeneration

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

Developmental programming: Prenatal Testosterone Excess Disrupts Pancreatic Islet Developmental Trajectory in Female Sheep

Por Jackson, Ian J, Puttabytappa, Muraly, Anderson, Miranda, Muralidharan, Meha, Veiga-Lopez, Almudena, Gregg, Brigid, Limesand, Sean, Padmanabhan, Vasantha
Publicado no Mol Cell Endocrinol (2020)

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

Por Manolakou, Katerina, Beaton, Jenny, McConnell, Irene, Farquar, Christine, Manson, Jean, Hastie, Nicholas D., Bruce, Moira, Jackson, Ian J.
Publicado em 2001

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 em 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 no Pigment Cell Melanoma Res (2015)

Diphthamide Modification of EEF2 Requires a J-domain Protein and is Essential for Normal Development

Por Webb, Tom R, Cross, Sally H., McKie, Lisa, Edgar, Ruth, Vizor, Lucie, Harrison, Jackie, Peters, Jo, Jackson, Ian J.
Publicado em 2008

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 em 2014

A CNS-Specific Hypomorphic Pdgfr-Beta Mutant Model of Diabetic Retinopathy

Por Jadeja, Shalini, Mort, Richard L., Keighren, Margaret, Hart, Alan W., Joynson, Russell, Wells, Sara, Potter, Paul K., Jackson, Ian J.
Publicado em 2013

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 no Nat Commun (2018)

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

Por Taylor, Kerrie L., Lister, James A., Zeng, Zhiqiang, Ishizaki, Hironori, Anderson, Caroline, Kelsh, Robert N., Jackson, Ian J., Patton, E. Elizabeth
Publicado em 2011

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 em 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 no Open Biol (2015)