α-synuclein levels affect autophagosome numbers in vivo and modulate Huntington disease pathology
Corrochano, Silvia, Renna, Maurizio, Tomas-Zapico, Cristina, Brown, Steve D.M., Lucas, Jose J., Rubinsztein, David C., Acevedo-Arozena, Abraham
Published in Autophagy (01.03.2012)
Published in Autophagy (01.03.2012)
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The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype
CROSS, Sally H, MCKIE, Lisa, WEST, Katrine, COGHILL, Emma L, FAVOR, Jack, BHATTACHARYA, Shoumo, BROWN, Steve D. M, JACKSON, Ian J
Published in Human molecular genetics (15.01.2011)
Published in Human molecular genetics (15.01.2011)
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VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5
Szumska, Dorota, Pieles, Guido, Essalmani, Rachid, Bilski, Michal, Mesnard, Daniel, Kaur, Kulvinder, Franklyn, Angela, El Omari, Kamel, Jefferis, Joanna, Bentham, Jamie, Taylor, Jennifer M, Schneider, Jurgen E, Arnold, Sebastian J, Johnson, Paul, Tymowska-Lalanne, Zuzanna, Stammers, Dave, Clarke, Kieran, Neubauer, Stefan, Morris, Andrew, Brown, Steve D, Shaw-Smith, Charles, Cama, Armando, Capra, Valeria, Ragoussis, Jiannis, Constam, Daniel, Seidah, Nabil G, Prat, Annik, Bhattacharya, Shoumo
Published in Genes & development (01.06.2008)
Published in Genes & development (01.06.2008)
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Novel Mouse Model of Autosomal Semidominant Adult Hypophosphatasia Has a Splice Site Mutation in the Tissue Nonspecific Alkaline Phosphatase Gene Akp2
Hough, Tertius A, Polewski, Monika, Johnson, Kristen, Cheeseman, Michael, Nolan, Patrick M, Vizor, Lucie, Rastan, Sohaila, Boyde, Alan, Pritzker, Kenneth, Hunter, A Jackie, Fisher, Elizabeth MC, Terkeltaub, Robert, Brown, Steve DM
Published in Journal of bone and mineral research (01.09.2007)
Published in Journal of bone and mineral research (01.09.2007)
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Regulatory variation at glypican-3 underlies a major growth QTL in mice
Oliver, Fiona, Christians, Julian K, Liu, Xiaojun, Rhind, Susan, Verma, Vinesh, Davison, Claire, Brown, Steve D M, Denny, Paul, Keightley, Peter D
Published in PLoS biology (01.05.2005)
Published in PLoS biology (01.05.2005)
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An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda
Barbaric, Ivana, Perry, Mark J, Dear, T. Neil, Rodrigues Da Costa, Alexandra, Salopek, Daniela, Marusic, Ana, Hough, Tertius, Wells, Sara, Hunter, A. Jackie, Cheeseman, Michael, Brown, Steve D. M
Published in Physiological genomics (19.02.2008)
Published in Physiological genomics (19.02.2008)
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A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11
Bhutta, Mahmood F., Lambie, Jane, Hobson, Lindsey, Goel, Anuj, Hafrén, Lena, Einarsdottir, Elisabet, Mattila, Petri S., Farrall, Martin, Brown, Steve, Burton, Martin J.
Published in Scientific reports (02.10.2017)
Published in Scientific reports (02.10.2017)
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Care coordinator assistants: Job satisfaction and the importance of teamwork in delivering person-centered dementia care
Nowaskie, Dustin, Carvell, Carly A, Alder, Catherine A, LaMantia, Michael A, Gao, Sujuan, Brown, Steve, Boustani, Malaz A, Austrom, Mary Guerriero
Published in Dementia (London, England) (01.07.2020)
Published in Dementia (London, England) (01.07.2020)
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Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Spielmann, Nadine, Miller, Gregor, Oprea, Tudor I, Hsu, Chih-Wei, Fobo, Gisela, Frishman, Goar, Montrone, Corinna, Haseli Mashhadi, Hamed, Mason, Jeremy, Munoz Fuentes, Violeta, Leuchtenberger, Stefanie, Ruepp, Andreas, Wagner, Matias, Westphal, Dominik S, Wolf, Cordula, Görlach, Agnes, Sanz-Moreno, Adrián, Cho, Yi-Li, Teperino, Raffaele, Brandmaier, Stefan, Sharma, Sapna, Galter, Isabella Rikarda, Östereicher, Manuela A, Zapf, Lilly, Mayer-Kuckuk, Philipp, Rozman, Jan, Teboul, Lydia, Bunton-Stasyshyn, Rosie K A, Cater, Heather, Stewart, Michelle, Christou, Skevoulla, Westerberg, Henrik, Willett, Amelia M, Wotton, Janine M, Roper, Willson B, Christiansen, Audrey E, Ward, Christopher S, Heaney, Jason D, Reynolds, Corey L, Prochazka, Jan, Bower, Lynette, Clary, David, Selloum, Mohammed, Bou About, Ghina, Wendling, Olivia, Jacobs, Hugues, Leblanc, Sophie, Meziane, Hamid, Sorg, Tania, Audain, Enrique, Gilly, Arthur, Rayner, Nigel W, Hitz, Marc-Phillip, Zeggini, Eleftheria, Wolf, Eckhard, Sedlacek, Radislav, Murray, Steven A, Svenson, Karen L, Braun, Robert E, White, Jaqueline K, Kelsey, Lois, Gao, Xiang, Shiroishi, Toshihiko, Xu, Ying, Seong, Je Kyung, Mammano, Fabio, Tocchini-Valentini, Glauco P, Beaudet, Arthur L, Meehan, Terrence F, Parkinson, Helen, Smedley, Damian, Mallon, Ann-Marie, Wells, Sara E, Grallert, Harald, Wurst, Wolfgang, Marschall, Susan, Fuchs, Helmut, Brown, Steve D M, Flenniken, Ann M, Nutter, Lauryl M J, McKerlie, Colin, Herault, Yann, Lloyd, K C Kent, Dickinson, Mary E, Gailus-Durner, Valerie, Hrabe de Angelis, Martin
Published in Nature cardiovascular research (01.02.2022)
Published in Nature cardiovascular research (01.02.2022)
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An N‐Ethyl‐N‐Nitrosourea (ENU)‐Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice
Gorvin, Caroline M, Ahmad, Bushra N, Stechman, Michael J, Loh, Nellie Y, Hough, Tertius A, Leo, Paul, Marshall, Mhairi, Sethi, Siddharth, Bentley, Liz, Piret, Sian E, Reed, Anita, Jeyabalan, Jeshmi, Christie, Paul T, Wells, Sara, Simon, Michelle M, Mallon, Ann‐Marie, Schulz, Herbert, Huebner, Norbert, Brown, Matthew A, Cox, Roger D, Brown, Steve D, Thakker, Rajesh V
Published in Journal of bone and mineral research (01.03.2019)
Published in Journal of bone and mineral research (01.03.2019)
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Absence of Embigin accelerates hearing loss and causes sub-viability, brain and heart defects in C57BL/6N mice due to interaction with Cdh23ahl
Newton, Sherylanne, Aguilar, Carlos, Bunton-Stasyshyn, Rosie K., Flook, Marisa, Stewart, Michelle, Marcotti, Walter, Brown, Steve, Bowl, Michael R.
Published in iScience (20.10.2023)
Published in iScience (20.10.2023)
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Protein 4.1 expression in the developing hair cells of the mouse inner ear
Okumura, Kazuhiro, Mochizuki, Eiji, Yokohama, Michinari, Yamakawa, Hisashi, Shitara, Hiroshi, Mburu, Philomena, Yonekawa, Hiromichi, Brown, Steve D.M, Kikkawa, Yoshiaki
Published in Brain research (11.01.2010)
Published in Brain research (11.01.2010)
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A mutation in Nischarin causes otitis media via LIMK1 and NF-KB pathways
Crompton, Michael, Purnell, Tom, Tyrer, Hayley E, Parker, Andrew, Ball, Greg, Hardisty-Hughes, Rachel E, Gale, Richard, Williams, Debbie, Dean, Charlotte H, Simon, Michelle M, Mallon, Ann-Marie, Wells, Sara, Bhutta, Mahmood F, Burton, Martin J, Tateossian, Hilda, Brown, Steve D M
Published in PLoS genetics (01.08.2017)
Published in PLoS genetics (01.08.2017)
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Non-drug therapies for the management of chronic constipation in adults: the CapaCiTY research programme including three RCTs
Knowles, Charles H, Booth, Lesley, Brown, Steve R, Cross, Samantha, Eldridge, Sandra, Emmett, Christopher, Grossi, Ugo, Jordan, Mary, Lacy-Colson, Jon, Mason, James, McLaughlin, John, Moss-Morris, Rona, Norton, Christine, Scott, S Mark, Stevens, Natasha, Taheri, Shiva, Yiannakou, Yan
Published in Programme grants for applied research (01.11.2021)
Published in Programme grants for applied research (01.11.2021)
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Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells
Geng, Ruishuang, Sotomayor, Marcos, Kinder, Kimberly J, Gopal, Suhasini R, Gerka-Stuyt, John, Chen, Daniel H-C, Hardisty-Hughes, Rachel E, Ball, Greg, Parker, Andy, Gaudet, Rachelle, Furness, David, Brown, Steve D, Corey, David P, Alagramam, Kumar N
Published in The Journal of neuroscience (06.03.2013)
Published in The Journal of neuroscience (06.03.2013)
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N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 ( Ap2s1 ) Mutations Establish Ap2s1 Loss-of-Function Mice
Gorvin, Caroline M, Rogers, Angela, Stewart, Michelle, Paudyal, Anju, Hough, Tertius A, Teboul, Lydia, Wells, Sara, Brown, Steve Dm, Cox, Roger D, Thakker, Rajesh V
Published in JBMR plus (01.08.2017)
Published in JBMR plus (01.08.2017)
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Panel 4: Recent advances in otitis media in molecular biology, biochemistry, genetics, and animal models
Li, Jian-Dong, Hermansson, Ann, Ryan, Allen F, Bakaletz, Lauren O, Brown, Steve D, Cheeseman, Michael T, Juhn, Steven K, Jung, Timothy T K, Lim, David J, Lim, Jae Hyang, Lin, Jizhen, Moon, Sung-Kyun, Post, J Christopher
Published in Otolaryngology-head and neck surgery (01.04.2013)
Published in Otolaryngology-head and neck surgery (01.04.2013)
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