Filamin A Regulates Neural Progenitor Proliferation and Cortical Size through Wee1-Dependent Cdk1 Phosphorylation

по Lian, Gewei, Lu, Jie, Hu, Jianjun, Zhang, Jingping, Cross, Sally H., Ferland, Russell J., Sheen, Volney L.
Опубликовано 2012

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

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

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

по Findlay, Amy S., McKie, Lisa, Keighren, Margaret, Clementson-Mobbs, Sharon, Sanchez-Pulido, Luis, Wells, Sara, Cross, Sally H., Jackson, Ian J.
Опубликовано в: Sci Rep (2020)

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype

по Cross, Sally H., McKie, Lisa, West, Katrine, Coghill, Emma L., Favor, Jack, Bhattacharya, Shoumo, Brown, Steve D.M., Jackson, Ian J.
Опубликовано 2011

Normal X-inactivation mosaicism in corneas of heterozygous Flna(Dilp2/+ )female mice--a model of human Filamin A (FLNA) diseases

по Douvaras, Panagiotis, Liu, Weijia, Mort, Richard L, McKie, Lisa, West, Katrine M, Cross, Sally H, Morley, Steven D, West, John D
Опубликовано 2012

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

по Cross, Sally H., Mckie, Lisa, Keighren, Margaret, West, Katrine, Thaung, Caroline, Davey, Tracey, Soares, Dinesh C., Sanchez-Pulido, Luis, Jackson, Ian J.
Опубликовано в: Invest Ophthalmol Vis Sci (2019)

The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cells

по Parker, Andrew, Cross, Sally H., Jackson, Ian J., Hardisty-Hughes, Rachel, Morse, Susan, Nicholson, George, Coghill, Emma, Bowl, Michael R., Brown, Steve D. M.
Опубликовано в: Dis Model Mech (2015)

The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification

по Cross, Sally H., Mckie, Lisa, Hurd, Toby W., Riley, Sam, Wills, Jimi, Barnard, Alun R., Young, Fiona, MacLaren, Robert E., Jackson, Ian J.
Опубликовано в: PLoS Genet (2020)

Mouse Slc9a8 Mutants Exhibit Retinal Defects Due to Retinal Pigmented Epithelium Dysfunction

по Jadeja, Shalini, Barnard, Alun R., McKie, Lisa, Cross, Sally H., White, Jacqueline K., Robertson, Morag, Budd, Peter S., MacLaren, Robert E., Jackson, Ian J.
Опубликовано в: Invest Ophthalmol Vis Sci (2015)

A meckelin–filamin A interaction mediates ciliogenesis

по Adams, Matthew, Simms, Roslyn J., Abdelhamed, Zakia, Dawe, Helen R., Szymanska, Katarzyna, Logan, Clare V., Wheway, Gabrielle, Pitt, Eva, Gull, Keith, Knowles, Margaret A., Blair, Edward, Cross, Sally H., Sayer, John A., Johnson, Colin A.
Опубликовано 2012

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function

по 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.
Опубликовано в: Dis Model Mech (2018)

Genetic background modifies vulnerability to glaucoma-related phenotypes in Lmx1b mutant mice

по 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.
Опубликовано в: Dis Model Mech (2021)

A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation

по Cross, Sally H., Macalinao, Danilo G., McKie, Lisa, Rose, Lorraine, Kearney, Alison L., Rainger, Joe, Thaung, Caroline, Keighren, Margaret, Jadeja, Shalini, West, Katrine, Kneeland, Stephen C., Smith, Richard S., Howell, Gareth R., Young, Fiona, Robertson, Morag, van t' Hof, Rob, John, Simon W. M., Jackson, Ian J.
Опубликовано 2014

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

по 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.
Опубликовано в: Nat Commun (2016)

Genomic anatomy of the Tyrp1 (brown) deletion complex

по Smyth, Ian M., Wilming, Laurens, Lee, Angela W., Taylor, Martin S., Gautier, Phillipe, Barlow, Karen, Wallis, Justine, Martin, Sancha, Glithero, Rebecca, Phillimore, Ben, Pelan, Sarah, Andrew, Rob, Holt, Karen, Taylor, Ruth, McLaren, Stuart, Burton, John, Bailey, Jonathon, Sims, Sarah, Squares, Jan, Plumb, Bob, Joy, Ann, Gibson, Richard, Gilbert, James, Hart, Elizabeth, Laird, Gavin, Loveland, Jane, Mudge, Jonathan, Steward, Charlie, Swarbreck, David, Harrow, Jennifer, North, Philip, Leaves, Nicholas, Greystrong, John, Coppola, Maria, Manjunath, Shilpa, Campbell, Mark, Smith, Mark, Strachan, Gregory, Tofts, Calli, Boal, Esther, Cobley, Victoria, Hunter, Giselle, Kimberley, Christopher, Thomas, Daniel, Cave-Berry, Lee, Weston, Paul, Botcherby, Marc R. M., White, Sharon, Edgar, Ruth, Cross, Sally H., Irvani, Marjan, Hummerich, Holger, Simpson, Eleanor H., Johnson, Dabney, Hunsicker, Patricia R., Little, Peter F. R., Hubbard, Tim, Campbell, R. Duncan, Rogers, Jane, Jackson, Ian J.
Опубликовано 2006