未登录 Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineage 基因工程的Pmel多顺反子等位基因在黑素细胞谱系中产生高度特异性的CreERT2-mediated重组 Wilkinson, Emma L.; Brennan, Louise C.; Harrison, Olivia J.; Crane-Smith, Zoe; Gautier, Philippe; Keighren, Margaret A.; Budd, Peter; Swaminathan, Karthic; Machesky, Laura M.; Allinson, Sarah L.; Jackson, Ian J.; Mort, Richard L. 分享 收藏
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Dopachrome tautomerase variants in patients with oculocutaneous albinism 眼皮肤白化病患者的Dopachrome互变异构酶变体 Pennamen, Perrine; Tingaud-Sequeira, Angele; Gazova, Iveta; Keighren, Margaret; McKie, Lisa; Marlin, Sandrine; Gherbi Halem, Souad; Kaplan, Josseline; Delevoye, Cedric; Lacombe, Didier; Plaisant, Claudio; Michaud, Vincent; Lasseaux, Eulalie; Javerzat, Sophie; Jackson, Ian; Arveiler, Benoit 分享 收藏
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. 分享 收藏
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Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function Findlay, Amy S.; McKie, Lisa; Keighren, Margaret; Clementson-Mobbs, Sharon; Sanchez-Pulido, Luis; Wells, Sara; Cross, Sally H.; Jackson, Ian J. 分享 收藏
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Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice (vol 7, e1002114, 2011) 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; Megarbane, Andre; Semerci, C. Nur; Khan, Ayesha; Zafar, Saemah; Hennekam, Raoul; Sousa, Sergio 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. 分享 收藏
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A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice Ford, Matthew J.; Yeyati, Patricia L.; Mali, Girish R.; Keighren, Margaret A.; Waddell, Scott H.; Mjoseng, Heidi K.; Douglas, Adam T.; Hall, Emma A.; Sakaue-Sawano, Asako; Miyawaki, Atsushi; Meehan, Richard R.; Boulter, Luke; Jackson, Ian J.; Mill, Pleasantine; Mort, Richard L. 分享 收藏
Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function Findlay, Amy S.; Carter, Roderick N.; Starbuck, Becky; McKie, Lisa; Novakova, Klara; Budd, Peter S.; Keighren, Margaret A.; Marsh, Joseph A.; Cross, Sally H.; Simon, Michelle M.; Potter, Paul K.; Morton, Nicholas M.; Jackson, Ian J. 分享 收藏
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PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins Hall, Emma A.; Nahorski, Michael S.; Murray, Lyndsay M.; Shaheen, Ranad; Perkins, Emma; Dissanayake, Kosala N.; Kristaryanto, Yosua; Jones, Ross A.; Vogt, Julie; Rivagorda, Manon; Handley, Mark T.; Mali, Girish R.; Quidwai, Tooba; Soares, Dinesh C.; Keighren, Margaret A.; McKie, Lisa; Mort, Richard L.; Gammoh, Noor; Garcia-Munoz, Amaya; Davey, Tracey; Vermeren, Matthieu; Walsh, Diana; Budd, Peter; Aligianis, Irene A.; Faqeih, Eissa; Quigley, Alan J.; Jackson, Ian J.; Kulathu, Yogesh; Jackson, Mandy; Ribchester, Richard R.; von Kriegsheim, Alex; Alkuraya, Fowzan S.; Woods, C. Geoffrey; Maher, Eamonn R.; Mill, Pleasantine 分享 收藏
KDM3A coordinates actin dynamics with intraflagellar transport to regulate cilia stability KDM3A协调肌动蛋白动力学与鞭毛内运输以调节纤毛稳定性 Yeyati, Patricia L.; Schiller, Rachel; Mali, Girish; Kasioulis, Ioannis; Kawamura, Akane; Adams, Ian R.; Playfoot, Christopher; Gilbert, Nick; van Heyningen, Veronica; Wills, Jimi; von Kriegsheim, Alex; Finch, Andrew; Sakai, Juro; Schofield, Christopher J.; Jackson, Ian J.; Mill, Pleasantine 分享 收藏
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease Potter, Paul K.; Bowl, Michael R.; Jeyarajan, Prashanthini; Wisby, Laura; Blease, Andrew; Goldsworthy, Michelle E.; Simon, Michelle M.; Greenaway, Simon; Michel, Vincent; Barnard, Alun; Aguilar, Carlos; Agnew, Thomas; Banks, Gareth; Blake, Andrew; Chessum, Lauren; Dorning, Joanne; Falcone, Sara; Goosey, Laurence; Harris, Shelley; Haynes, Andy; Heise, Ines; Hillier, Rosie; Hough, Tertius; Hoslin, Angela; Hutchison, Marie; King, Ruairidh; Kumar, Saumya; Lad, Heena V.; Law, Gemma; MacLaren, Robert E.; Morse, Susan; Nicol, Thomas; Parker, Andrew; Pickford, Karen; Sethi, Siddharth; Starbuck, Becky; Stelma, Femke; Cheeseman, Michael; Cross, Sally H.; Foster, Russell G.; Jackson, Ian J.; Peirson, Stuart N.; Thakker, Rajesh V.; Vincent, Tonia; Scudamore, Cheryl; Wells, Sara; El-Amraoui, Aziz; Petit, Christine; Acevedo-Arozena, Abraham; Nolan, Patrick M.; Cox, Roger; Mallon, Anne-Marie; Brown, Steve D. M. 分享 收藏
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. 分享 收藏
Eye diseases identified in the ENU-Ageing Screen Jackson, I.; Starbuck, B.; McKie, L.; Banks, G.; Blease, A.; Simon, M.; Wisby, L.; Cross, S.; Nolan, P.; Brown, S.; Potter, P. 分享 收藏
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