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S

Sally H. Cross

University of Edinburgh

31H指数
77论文数
3.9K被引数
收录论文 23
发表时间
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Genetic background modifies vulnerability to glaucoma-related phenotypes in Lmx1b mutant mice
errDISEASE MODELS & MECHANISMS
IF3.3
err2021-02-19
err15
errOAAI
errTolman, 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.
err分享
err收藏
The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specification
errPLOS GENETICS
IF3.7
err2020-04-01
err19
errOAAI
errCross, Sally H.; Mckie, Lisa; Hurd, Toby W.; Riley, Sam; Wills, Jimi; Barnard, Alun R.; Young, Fiona; MacLaren, Robert E.; Jackson, Ian J.
err分享
err收藏
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function
errSCIENTIFIC REPORTS
IF3.9
err2020-01-16
err2
errOAAI
errFindlay, Amy S.; McKie, Lisa; Keighren, Margaret; Clementson-Mobbs, Sharon; Sanchez-Pulido, Luis; Wells, Sara; Cross, Sally H.; Jackson, Ian J.
err分享
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Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2019-07-02
err15
errOAAI
errCross, Sally H.; Mckie, Lisa; Keighren, Margaret; West, Katrine; Thaung, Caroline; Davey, Tracey; Soares, Dinesh C.; Sanchez-Pulido, Luis; Jackson, Ian J.
err分享
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Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function
errDISEASE MODELS & MECHANISMS
IF3.3
err2018-01-01
err26
errOAAI
errFindlay, 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.
err分享
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Novel gene function revealed by mouse mutagenesis screens for models of age-related disease
errNATURE COMMUNICATIONS
IF15.7
err2016-08-18
err67
errOAAI
errPotter, 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.
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Eye diseases identified in the ENU-Ageing Screen
errACTA OPHTHALMOLOGICA
IF2.8
err2015-09-23
err0
errOAAI
errJackson, I.; Starbuck, B.; McKie, L.; Banks, G.; Blease, A.; Simon, M.; Wisby, L.; Cross, S.; Nolan, P.; Brown, S.; Potter, P.
err分享
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Mouse Slc9a8 Mutants Exhibit Retinal Defects Due to Retinal Pigmented Epithelium Dysfunction小鼠Slc9a8突变体由于视网膜色素上皮功能障碍而表现出视网膜缺陷
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2015-05-13
err11
errOAAI
errJadeja, Shalini; Barnard, Alun R.; McKie, Lisa; Cross, Sally H.; White, Jacqueline K.; Robertson, Morag; Budd, Peter S.; MacLaren, Robert E.; Jackson, Ian J.
err分享
err收藏
The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cellsgoya小鼠突变体揭示了MAP3K1在耳蜗感觉毛细胞发育和存活中的独特作用
errDISEASE MODELS & MECHANISMS
IF3.3
err2015-01-01
err13
errOAAI
errParker, Andrew; Cross, Sally H.; Jackson, Ian J.; Hardisty-Hughes, Rachel; Morse, Susan; Nicholson, George; Coghill, Emma; Bowl, Michael R.; Brown, Steve D. M.
err分享
err收藏
A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation
errPLOS GENETICS
IF3.7
err2014-05-08
err26
errOAAI
errCross, 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.
err分享
err收藏
A meckelinfilamin A interaction mediates ciliogenesis
errHUMAN MOLECULAR GENETICS
IF3.2
err2011-11-25
err103
errOAAI
errAdams, 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.
err分享
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The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype
errHUMAN MOLECULAR GENETICS
IF3.2
err2010-10-13
err15
errOAAI
errCross, Sally H.; McKie, Lisa; West, Katrine; Coghill, Emma L.; Favor, Jack; Bhattacharya, Shoumo; Brown, Steve D. M.; Jackson, Ian J.
err分享
err收藏
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development
errJOURNAL OF CELL SCIENCE
IF3.6
err2008-10-01
err71
errOAAI
errWebb, Tom R.; Cross, Sally H.; McKie, Lisa; Edgar, Ruth; Vizor, Lucie; Harrison, Jackie; Peters, Jo; Jackson, Ian J.
err分享
err收藏
Cardiac malformations and midline skeletal defects in mice lacking filamin A
errHUMAN MOLECULAR GENETICS
IF3.2
err2006-07-06
err147
errOAAI
errHart, Alan W.; Morgan, Joanne E.; Schneider, Jurgen; West, Katrine; McKie, Lisa; Bhattacharya, Shoumo; Jackson, Ian J.; Cross, Sally H.
err分享
err收藏
Genomic anatomy of the Tyrp1 (brown) deletion complex
errPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
IF9.1
err2006-02-27
err30
errOAAI
errSmyth, IM; Wilming, L; Lee, AW; Taylor, MS; Gautier, P; Barlow, K; Wallis, J; Martin, S; Glithero, R; Phillimore, B; Pelan, S; Andrew, R; Holt, K; Taylor, R; McLaren, S; Burton, J; Bailey, J; Sims, S; Squares, J; Plumb, B; Joy, A; Gibson, R; Gilbert, J; Hart, E; Laird, G; Loveland, J; Mudge, J; Steward, C; Swarbreck, D; Harrow, J; North, P; Leaves, N; Greystrong, J; Coppola, M; Manjunath, S; Campbell, M; Smith, M; Strachan, G; Tofts, C; Boal, E; Cobley, V; Hunter, G; Kimberley, C; Thomas, D; Cave-Berry, L; Weston, P; Botcherby, MRM; White, S; Edgar, R; Cross, SH; Irvani, M; Hummerich, H; Simpson, EH; Johnson, D; Hunsicker, PR; Little, PFR; Hubbard, T; Campbell, RD; Rogers, J; Jackson, IJ
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Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy
errHUMAN MOLECULAR GENETICS
IF3.2
err2005-09-13
err126
PREAI
errVan Agtmael, T; Schlötzer-Schrehardt, U; McKie, L; Brownstein, DG; Lee, AW; Cross, SH; Sado, Y; Mullins, JJ; Pöschl, E; Jackson, IJ
err分享
err收藏
Genotype-phenotype correlation of mouse Pde6b mutations
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2005-09-01
err79
PREAI
errHart, AW; McKie, L; Morgan, JE; Gautier, P; West, K; Jackson, IJ; Cross, SH
err分享
err收藏
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion:: mechanistic insights into human congenital central hypoventilation syndrome
errHUMAN MOLECULAR GENETICS
IF3.2
err2004-05-05
err29
errOAAI
errCross, SH; Morgan, JE; Pattyn, A; West, K; McKie, L; Hart, A; Thaung, C; Brunet, JF; Jackson, IJ
err分享
err收藏
THE EFFECTS OF DEUTERIUM SUBSTITUTION ON THE RATES OF ORGANIC REACTIONS .5. HYDROLYSIS OF ALPHA-DEUTERO KETALS
errJOURNAL OF THE AMERICAN CHEMICAL SOCIETY
IF15.6
err2002-05-01
err40
PREAI
errSHINER, VJ; CROSS, S
err分享
err收藏
Isolation of CpG islands from large genomic clones
errNUCLEIC ACIDS RESEARCH
IF13.1
err1999-01-01
err61
errOAAI
errCross, SH; Clark, VH; Bird, AP
err分享
err收藏

研究方向

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合作学者
合作期刊
A
Adrian Bird
H 指数: 114 · 论文数: 317
R
Rajesh V. Thakker
H 指数: 100 · 论文数: 839
C
Christine Petit
H 指数: 99 · 论文数: 638
T
Tim Hubbard
H 指数: 94 · 论文数: 308
K
Keith Gull
H 指数: 88 · 论文数: 906
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