The melanocyte lineage in development and disease
Mort, Richard L, Jackson, Ian J, Patton, E Elizabeth
Published in Development (Cambridge) (15.02.2015)
Published in Development (Cambridge) (15.02.2015)
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Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability
Morgan, Michael D., Pairo-Castineira, Erola, Rawlik, Konrad, Canela-Xandri, Oriol, Rees, Jonathan, Sims, David, Tenesa, Albert, Jackson, Ian J.
Published in Nature communications (10.12.2018)
Published in Nature communications (10.12.2018)
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Mouse genomic variation and its effect on phenotypes and gene regulation
Keane, Thomas M., Goodstadt, Leo, Danecek, Petr, White, Michael A., Wong, Kim, Yalcin, Binnaz, Heger, Andreas, Agam, Avigail, Slater, Guy, Goodson, Martin, Furlotte, Nicholas A., Eskin, Eleazar, Nellåker, Christoffer, Whitley, Helen, Cleak, James, Janowitz, Deborah, Hernandez-Pliego, Polinka, Edwards, Andrew, Belgard, T. Grant, Oliver, Peter L., McIntyre, Rebecca E., Bhomra, Amarjit, Nicod, Jérôme, Gan, Xiangchao, Yuan, Wei, van der Weyden, Louise, Steward, Charles A., Bala, Sendu, Stalker, Jim, Mott, Richard, Durbin, Richard, Jackson, Ian J., Czechanski, Anne, Guerra-Assunção, José Afonso, Donahue, Leah Rae, Reinholdt, Laura G., Payseur, Bret A., Ponting, Chris P., Birney, Ewan, Flint, Jonathan, Adams, David J.
Published in Nature (London) (15.09.2011)
Published in Nature (London) (15.09.2011)
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Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes
Hall, Emma A, Keighren, Margaret, Ford, Matthew J, Davey, Tracey, Jarman, Andrew P, Smith, Lee B, Jackson, Ian J, Mill, Pleasantine
Published in PLoS genetics (01.12.2013)
Published in PLoS genetics (01.12.2013)
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Signatures of diversifying selection in European pig breeds
Wilkinson, Samantha, Lu, Zen H, Megens, Hendrik-Jan, Archibald, Alan L, Haley, Chris, Jackson, Ian J, Groenen, Martien A M, Crooijmans, Richard P M A, Ogden, Rob, Wiener, Pamela
Published in PLoS genetics (01.04.2013)
Published in PLoS genetics (01.04.2013)
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A Conditional Zebrafish MITF Mutation Reveals MITF Levels Are Critical for Melanoma Promotion vs. Regression In Vivo
Lister, James A., Capper, Amy, Zeng, Zhiqiang, Mathers, Marie E., Richardson, Jennifer, Paranthaman, Karthika, Jackson, Ian J., Elizabeth Patton, E.
Published in Journal of investigative dermatology (01.01.2014)
Published in Journal of investigative dermatology (01.01.2014)
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Genetic background influences age-related decline in visual and nonvisual retinal responses, circadian rhythms, and sleep
Banks, Gareth, Heise, Ines, Starbuck, Becky, Osborne, Tamzin, Wisby, Laura, Potter, Paul, Jackson, Ian J, Foster, Russell G, Peirson, Stuart N, Nolan, Patrick M
Published in Neurobiology of aging (01.01.2015)
Published in Neurobiology of aging (01.01.2015)
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The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification
Cross, Sally H, Mckie, Lisa, Hurd, Toby W, Riley, Sam, Wills, Jimi, Barnard, Alun R, Young, Fiona, MacLaren, Robert E, Jackson, Ian J
Published in PLoS genetics (01.04.2020)
Published in PLoS genetics (01.04.2020)
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Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model
Mort, Richard L., Ross, Robert J. H., Hainey, Kirsten J., Harrison, Olivia J., Keighren, Margaret A., Landini, Gabriel, Baker, Ruth E., Painter, Kevin J., Jackson, Ian J., Yates, Christian A.
Published in Nature communications (06.01.2016)
Published in Nature communications (06.01.2016)
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Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis
Mill, Pleasantine, Lockhart, Paul J., Fitzpatrick, Elizabeth, Mountford, Hayley S., Hall, Emma A., Reijns, Martin A.M., Keighren, Margaret, Bahlo, Melanie, Bromhead, Catherine J., Budd, Peter, Aftimos, Salim, Delatycki, Martin B., Savarirayan, Ravi, Jackson, Ian J., Amor, David J.
Published in American journal of human genetics (08.04.2011)
Published in American journal of human genetics (08.04.2011)
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A mouse model of brittle cornea syndrome caused by mutation in Zfp469
Stanton, Chloe M, Findlay, Amy S, Drake, Camilla, Mustafa, Mohammad Z, Gautier, Philippe, McKie, Lisa, Jackson, Ian J, Vitart, Veronique
Published in Disease models & mechanisms (01.09.2021)
Published in Disease models & mechanisms (01.09.2021)
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Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss
Chen, Jing, Ingham, Neil, Kelly, John, Jadeja, Shalini, Goulding, David, Pass, Johanna, Mahajan, Vinit B, Tsang, Stephen H, Nijnik, Anastasia, Jackson, Ian J, White, Jacqueline K, Forge, Andrew, Jagger, Daniel, Steel, Karen P
Published in PLoS genetics (01.10.2014)
Published in PLoS genetics (01.10.2014)
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P-Rex1 is required for efficient melanoblast migration and melanoma metastasis
Lindsay, Colin R., Lawn, Samuel, Campbell, Andrew D., Faller, William J., Rambow, Florian, Mort, Richard L., Timpson, Paul, Li, Ang, Cammareri, Patrizia, Ridgway, Rachel A., Morton, Jennifer P., Doyle, Brendan, Hegarty, Shauna, Rafferty, Mairin, Murphy, Ian G., McDermott, Enda W., Sheahan, Kieran, Pedone, Katherine, Finn, Alexander J., Groben, Pamela A., Thomas, Nancy E., Hao, Honglin, Carson, Craig, Norman, Jim C., Machesky, Laura M., Gallagher, William M., Jackson, Ian J., Van Kempen, Leon, Beermann, Friedrich, Der, Channing, Larue, Lionel, Welch, Heidi C., Ozanne, Brad W., Sansom, Owen J.
Published in Nature communications (22.11.2011)
Published in Nature communications (22.11.2011)
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Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice
Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, Fitzpatrick, David R
Published in PLoS genetics (01.07.2011)
Published in PLoS genetics (01.07.2011)
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Journal Article
Rac1 Drives Melanoblast Organization during Mouse Development by Orchestrating Pseudopod- Driven Motility and Cell-Cycle Progression
Li, Ang, Ma, Yafeng, Yu, Xinzi, Mort, Richard L., Lindsay, Colin R., Stevenson, David, Strathdee, Douglas, Insall, Robert H., Chernoff, Jonathan, Snapper, Scott B., Jackson, Ian J., Larue, Lionel, Sansom, Owen J., Machesky, Laura M.
Published in Developmental cell (18.10.2011)
Published in Developmental cell (18.10.2011)
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Journal Article
HEATR2 plays a conserved role in assembly of the ciliary motile apparatus
Diggle, Christine P, Moore, Daniel J, Mali, Girish, zur Lage, Petra, Ait-Lounis, Aouatef, Schmidts, Miriam, Shoemark, Amelia, Garcia Munoz, Amaya, Halachev, Mihail R, Gautier, Philippe, Yeyati, Patricia L, Bonthron, David T, Carr, Ian M, Hayward, Bruce, Markham, Alexander F, Hope, Jilly E, von Kriegsheim, Alex, Mitchison, Hannah M, Jackson, Ian J, Durand, Bénédicte, Reith, Walter, Sheridan, Eamonn, Jarman, Andrew P, Mill, Pleasantine
Published in PLoS genetics (01.09.2014)
Published in PLoS genetics (01.09.2014)
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Genetic background modifies vulnerability to glaucoma-related phenotypes in Lmx1b mutant mice
Tolman, Nicholas G, Balasubramanian, Revathi, Macalinao, Danilo G, Kearney, Alison L, MacNicoll, Katharine H, Montgomery, Christa L, de Vries, Wilhelmine N, Jackson, Ian J, Cross, Sally H, Kizhatil, Krishnakumar, Nair, K Saidas, John, Simon W M
Published in Disease models & mechanisms (19.02.2021)
Published in Disease models & mechanisms (19.02.2021)
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Dominant role of the niche in melanocyte stem-cell fate determination
Nishikawa, Shin-Ichi, Nishimura, Emi K, Jordan, Siobhán A, Oshima, Hideo, Yoshida, Hisahiro, Osawa, Masatake, Moriyama, Mariko, Jackson, Ian J, Barrandon, Yann, Miyachi, Yoshiki
Published in Nature (London) (25.04.2002)
Published in Nature (London) (25.04.2002)
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Journal Article
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulation
Handley, Mark T., Carpanini, Sarah M., Mali, Girish R., Sidjanin, Duska J., Aligianis, Irene A., Jackson, Ian J., FitzPatrick, David R.
Published in Open biology (01.06.2015)
Published in Open biology (01.06.2015)
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