Gametogenesis and the Early Embryo

ανά Jackson, Ian J
Έκδοση 1988

Ex vivo live imaging of melanoblast migration in embryonic mouse skin

ανά Mort, Richard L, Hay, Leonard, Jackson, Ian J
Έκδοση 2010

The melanocyte lineage in development and disease

ανά Mort, Richard L., Jackson, Ian J., Patton, E. Elizabeth
Τόπος έκδοσης Development (2015)

The melanocyte lineage in development and disease

ανά Mort, Richard L., Jackson, Ian J., Patton, E. Elizabeth
Τόπος έκδοσης Development (2015)

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

ανά Mort, Richard L., Keighren, Margaret, Hay, Leonard, Jackson, Ian J.
Έκδοση 2014

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

ανά Delaney, Ada, Keighren, Margaret, Fleetwood-Walker, Susan M., Jackson, Ian J.
Έκδοση 2010

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

ανά Smyth, Ian, Du, Xin, Taylor, Martin S., Justice, Monica J., Beutler, Bruce, Jackson, Ian J.
Έκδοση 2004

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

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

A zebrafish model for nevus regeneration

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

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

ανά Jackson, Ian J, Puttabytappa, Muraly, Anderson, Miranda, Muralidharan, Meha, Veiga-Lopez, Almudena, Gregg, Brigid, Limesand, Sean, Padmanabhan, Vasantha
Τόπος έκδοσης Mol Cell Endocrinol (2020)

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

ανά Manolakou, Katerina, Beaton, Jenny, McConnell, Irene, Farquar, Christine, Manson, Jean, Hastie, Nicholas D., Bruce, Moira, Jackson, Ian J.
Έκδοση 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

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

Maintenance of distinct melanocyte populations in the interfollicular epidermis

ανά Glover, James D., Knolle, Stefan, Wells, Kirsty L., Liu, Dianbo, Jackson, Ian J., Mort, Richard L., Headon, Denis J.
Τόπος έκδοσης Pigment Cell Melanoma Res (2015)

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

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

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

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

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

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

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

ανά Morgan, Michael D., Pairo-Castineira, Erola, Rawlik, Konrad, Canela-Xandri, Oriol, Rees, Jonathan, Sims, David, Tenesa, Albert, Jackson, Ian J.
Τόπος έκδοσης Nat Commun (2018)

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

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

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

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

Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation

ανά Handley, Mark T., Carpanini, Sarah M., Mali, Girish R., Sidjanin, Duska J., Aligianis, Irene A., Jackson, Ian J., FitzPatrick, David R.
Τόπος έκδοσης Open Biol (2015)