Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background
Falcone, Sara, Wisby, Laura, Nicol, Thomas, Blease, Andrew, Starbuck, Becky, Parker, Andrew, Sanderson, Jeremy, Brown, Steve D M, Scudamore, Cheryl L, Pusey, Charles D, Tam, Frederick W K, Potter, Paul K
Published in Scientific reports (31.12.2019)
Published in Scientific reports (31.12.2019)
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Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function
Findlay, Amy S, Carter, Roderick N, Starbuck, Becky, McKie, Lisa, Nováková, Klára, Budd, Peter S, Keighren, Margaret A, Marsh, Joseph A, Cross, Sally H, Simon, Michelle M, Potter, Paul K, Morton, Nicholas M, Jackson, Ian J
Published in Disease models & mechanisms (01.12.2018)
Published in Disease models & mechanisms (01.12.2018)
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HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutants
Cheeseman, Michael T, Tyrer, Hayley E, Williams, Debbie, Hough, Tertius A, Pathak, Paras, Romero, Maria R, Hilton, Helen, Bali, Sulzhan, Parker, Andrew, Vizor, Lucie, Purnell, Tom, Vowell, Kate, Wells, Sara, Bhutta, Mahmood F, Potter, Paul K, Brown, Steve D M
Published in PLoS genetics (01.10.2011)
Published in PLoS genetics (01.10.2011)
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Pleiotropic brain function of whirlin identified by a novel mutation
Aguilar, Carlos, Williams, Debbie, Kurapati, Ramakrishna, Bains, Rasneer S., Mburu, Philomena, Parker, Andy, Williams, Jackie, Concas, Danilo, Tateossian, Hilda, Haynes, Andrew R., Banks, Gareth, Vikhe, Pratik, Heise, Ines, Hutchison, Marie, Atkins, Gemma, Gillard, Simon, Starbuck, Becky, Oliveri, Simona, Blake, Andrew, Sethi, Siddharth, Kumar, Saumya, Bardhan, Tanaya, Jeng, Jing-Yi, Johnson, Stuart L., Corns, Lara F., Marcotti, Walter, Simon, Michelle, Wells, Sara, Potter, Paul K., Lad, Heena V.
Published in iScience (19.07.2024)
Published in iScience (19.07.2024)
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Predominant role of IgM‐dependent activation of the classical pathway in the clearance of dying cells by murine bone marrow‐derived macrophages in vitro
Quartier, Pierre, Potter, Paul K., Ehrenstein, Michael R., Walport, Mark J., Botto, Marina
Published in European journal of immunology (01.01.2005)
Published in European journal of immunology (01.01.2005)
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Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations
Bull, Katherine R, Rimmer, Andrew J, Siggs, Owen M, Miosge, Lisa A, Roots, Carla M, Enders, Anselm, Bertram, Edward M, Crockford, Tanya L, Whittle, Belinda, Potter, Paul K, Simon, Michelle M, Mallon, Ann-Marie, Brown, Steve D M, Beutler, Bruce, Goodnow, Christopher C, Lunter, Gerton, Cornall, Richard J
Published in PLoS genetics (01.01.2013)
Published in PLoS genetics (01.01.2013)
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Tissue-specific differences in the assembly of mitochondrial Complex I are revealed by a novel ENU mutation in ECSIT
Nicol, Thomas, Falcone, Sara, Blease, Andrew, Vikhe, Pratik, Civiletto, Gabriele, Omairi, Saleh Salman, Viscomi, Carlo, Patel, Ketan, Potter, Paul K
Published in Cardiovascular research (16.10.2023)
Published in Cardiovascular research (16.10.2023)
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Journal Article
A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background
Falcone, Sara, Nicol, Thomas, Blease, Andrew, Randles, Michael J., Angus, Elizabeth, Page, Anton, Tam, Frederick W.K., Pusey, Charles D., Lennon, Rachel, Potter, Paul K.
Published in Kidney international (01.03.2022)
Published in Kidney international (01.03.2022)
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Chronically elevated branched chain amino acid levels are pro-arrhythmic
Portero, Vincent, Nicol, Thomas, Podliesna, Svitlana, Marchal, Gerard A, Baartscheer, Antonius, Casini, Simona, Tadros, Rafik, Treur, Jorien L, Tanck, Michael W T, Cox, I Jane, Probert, Fay, Hough, Tertius A, Falcone, Sara, Beekman, Leander, Müller-Nurasyid, Martina, Kastenmüller, Gabi, Gieger, Christian, Peters, Annette, Kääb, Stefan, Sinner, Moritz F, Blease, Andrew, Verkerk, Arie O, Bezzina, Connie R, Potter, Paul K, Remme, Carol Ann
Published in Cardiovascular research (22.06.2022)
Published in Cardiovascular research (22.06.2022)
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Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing
Nicod, Jérôme, Davies, Robert W, Cai, Na, Hassett, Carl, Goodstadt, Leo, Cosgrove, Cormac, Yee, Benjamin K, Lionikaite, Vikte, McIntyre, Rebecca E, Remme, Carol Ann, Lodder, Elisabeth M, Gregory, Jennifer S, Hough, Tertius, Joynson, Russell, Phelps, Hayley, Nell, Barbara, Rowe, Clare, Wood, Joe, Walling, Alison, Bopp, Nasrin, Bhomra, Amarjit, Hernandez-Pliego, Polinka, Callebert, Jacques, Aspden, Richard M, Talbot, Nick P, Robbins, Peter A, Harrison, Mark, Fray, Martin, Launay, Jean-Marie, Pinto, Yigal M, Blizard, David A, Bezzina, Connie R, Adams, David J, Franken, Paul, Weaver, Tom, Wells, Sara, Brown, Steve D M, Potter, Paul K, Klenerman, Paul, Lionikas, Arimantas, Mott, Richard, Flint, Jonathan
Published in Nature genetics (01.08.2016)
Published in Nature genetics (01.08.2016)
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Large-scale genomic investigation of pediatric cholestasis reveals a novel hepatorenal ciliopathy caused by PSKH1 mutations
Maddirevula, Sateesh, Shagrani, Mohammad, Ji, Ae-Ri, Horne, Christopher R., Young, Samuel N., Mather, Lucy J., Alqahtani, Mashael, McKerlie, Colin, Wood, Geoffrey, Potter, Paul K., Abdulwahab, Firdous, AlSheddi, Tarfa, van der Woerd, Wendy L., van Gassen, Koen L.I., AlBogami, Dalal, Kumar, Kishwer, Muhammad Akhtar, Ali Syed, Binomar, Hiba, Almanea, Hadeel, Faqeih, Eissa, Fuchs, Sabine A., Scott, John W., Murphy, James M., Alkuraya, Fowzan S.
Published in Genetics in medicine (09.08.2024)
Published in Genetics in medicine (09.08.2024)
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Quantifying Microsatellite Mutation Rates from Intestinal Stem Cell Dynamics in Msh2-Deficient Murine Epithelium
Christopher, Joseph, Thorsen, Ann-Sofie, Abujudeh, Sam, Lourenço, Filipe C, Kemp, Richard, Potter, Paul K, Morrissey, Edward, Hazelwood, Lee, Winton, Douglas J
Published in Genetics (Austin) (01.07.2019)
Published in Genetics (Austin) (01.07.2019)
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Journal Article
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
Published in Nature communications (18.08.2016)
Published in Nature communications (18.08.2016)
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Efficient clearance of opsonised apoptotic cells in the absence of PECAM-1
Potter, Paul K., Larbi, Karen Y., Nourshargh, Sussan, Botto, Marina
Published in Molecular Immunology (01.02.2007)
Published in Molecular Immunology (01.02.2007)
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Journal Article
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing
Simon, Michelle M., Moresco, Eva Marie Y., Bull, Katherine R., Kumar, Saumya, Mallon, Ann-Marie, Beutler, Bruce, Potter, Paul K.
Published in Mammalian Genome (01.10.2015)
Published in Mammalian Genome (01.10.2015)
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Book Review
With mouse age comes wisdom: A review and suggestions of relevant mouse models for age-related conditions
Drechsler, Susanne, Lynch, Marina A, Novella, Susana, González-Navarro, Herminia, Hecimovic, Silva, Barini, Erica, Tucci, Valter, Castro, Rui E, Vandenbroucke, Roosmarijn E., Osuchowski, Marcin, Potter, Paul K.
Published in Mechanisms of ageing and development (01.12.2016)
Published in Mechanisms of ageing and development (01.12.2016)
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Journal Article
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy
Jadeja, Shalini, Mort, Richard L, Keighren, Margaret, Hart, Alan W, Joynson, Russell, Wells, Sara, Potter, Paul K, Jackson, Ian J
Published in Investigative ophthalmology & visual science (01.05.2013)
Published in Investigative ophthalmology & visual science (01.05.2013)
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