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Items: 34

1.

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

Potter PK, Bowl MR, Jeyarajan P, Wisby L, Blease A, Goldsworthy ME, Simon MM, Greenaway S, Michel V, Barnard A, Aguilar C, Agnew T, Banks G, Blake A, Chessum L, Dorning J, Falcone S, Goosey L, Harris S, Haynes A, Heise I, Hillier R, Hough T, Hoslin A, Hutchison M, King R, Kumar S, Lad HV, Law G, MacLaren RE, Morse S, Nicol T, Parker A, Pickford K, Sethi S, Starbuck B, Stelma F, Cheeseman M, Cross SH, Foster RG, Jackson IJ, Peirson SN, Thakker RV, Vincent T, Scudamore C, Wells S, El-Amraoui A, Petit C, Acevedo-Arozena A, Nolan PM, Cox R, Mallon AM, Brown SD.

Nat Commun. 2016 Aug 18;7:12444. doi: 10.1038/ncomms12444.

2.

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

Parker A, Cross SH, Jackson IJ, Hardisty-Hughes R, Morse S, Nicholson G, Coghill E, Bowl MR, Brown SD.

Dis Model Mech. 2015 Dec;8(12):1555-68. doi: 10.1242/dmm.023176. Epub 2015 Nov 5.

3.

Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunction.

Jadeja S, Barnard AR, McKie L, Cross SH, White JK; Sanger Mouse Genetics Project, Robertson M, Budd PS, MacLaren RE, Jackson IJ.

Invest Ophthalmol Vis Sci. 2015 May;56(5):3015-26. doi: 10.1167/iovs.14-15735.

4.

A dominant-negative mutation of mouse Lmx1b causes glaucoma and is semi-lethal via LDB1-mediated dimerization [corrected].

Cross SH, Macalinao DG, McKie L, Rose L, Kearney AL, Rainger J, Thaung C, Keighren M, Jadeja S, West K, Kneeland SC, Smith RS, Howell GR, Young F, Robertson M, van T' Hof R, John SW, Jackson IJ.

PLoS Genet. 2014 May 8;10(5):e1004359. doi: 10.1371/journal.pgen.1004359. eCollection 2014 May. Erratum in: PLoS Genet. 2014 Dec;10(12):e1004917.

5.

Filamin a regulates neural progenitor proliferation and cortical size through Wee1-dependent Cdk1 phosphorylation.

Lian G, Lu J, Hu J, Zhang J, Cross SH, Ferland RJ, Sheen VL.

J Neurosci. 2012 May 30;32(22):7672-84. doi: 10.1523/JNEUROSCI.0894-12.2012.

6.

Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseases.

Douvaras P, Liu W, Mort RL, McKie L, West KM, Cross SH, Morley SD, West JD.

BMC Res Notes. 2012 Feb 27;5:122. doi: 10.1186/1756-0500-5-122.

7.

A meckelin-filamin A interaction mediates ciliogenesis.

Adams M, Simms RJ, Abdelhamed Z, Dawe HR, Szymanska K, Logan CV, Wheway G, Pitt E, Gull K, Knowles MA, Blair E, Cross SH, Sayer JA, Johnson CA.

Hum Mol Genet. 2012 Mar 15;21(6):1272-86. doi: 10.1093/hmg/ddr557. Epub 2011 Nov 25.

8.

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

Cross SH, McKie L, West K, Coghill EL, Favor J, Bhattacharya S, Brown SD, Jackson IJ.

Hum Mol Genet. 2011 Jan 15;20(2):223-34. doi: 10.1093/hmg/ddq457. Epub 2010 Oct 13.

9.

Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development.

Webb TR, Cross SH, McKie L, Edgar R, Vizor L, Harrison J, Peters J, Jackson IJ.

J Cell Sci. 2008 Oct 1;121(Pt 19):3140-5. doi: 10.1242/jcs.035550. Epub 2008 Sep 2.

10.

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Hart AW, Morgan JE, Schneider J, West K, McKie L, Bhattacharya S, Jackson IJ, Cross SH.

Hum Mol Genet. 2006 Aug 15;15(16):2457-67. Epub 2006 Jul 6.

PMID:
16825286
11.

Genomic anatomy of the Tyrp1 (brown) deletion complex.

Smyth 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 MR, White S, Edgar R, Cross SH, Irvani M, Hummerich H, Simpson EH, Johnson D, Hunsicker PR, Little PF, Hubbard T, Campbell RD, Rogers J, Jackson IJ.

Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3704-9. Epub 2006 Feb 27.

12.

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy.

Van Agtmael T, Schlötzer-Schrehardt U, McKie L, Brownstein DG, Lee AW, Cross SH, Sado Y, Mullins JJ, Pöschl E, Jackson IJ.

Hum Mol Genet. 2005 Nov 1;14(21):3161-8. Epub 2005 Sep 13.

PMID:
16159887
13.

Genotype-phenotype correlation of mouse pde6b mutations.

Hart AW, McKie L, Morgan JE, Gautier P, West K, Jackson IJ, Cross SH.

Invest Ophthalmol Vis Sci. 2005 Sep;46(9):3443-50. Erratum in: Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5170.

PMID:
16123450
14.

Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor.

Lee D, Cross SH, Strunk KE, Morgan JE, Bailey CL, Jackson IJ, Threadgill DW.

Mamm Genome. 2004 Jul;15(7):525-36.

PMID:
15366372
15.

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome.

Cross SH, Morgan JE, Pattyn A, West K, McKie L, Hart A, Thaung C, Brunet JF, Jackson IJ.

Hum Mol Genet. 2004 Jul 15;13(14):1433-9. Epub 2004 May 18.

PMID:
15150159
16.

Isolation of CpG islands from BAC clones using a methyl-CpG binding column.

Cross SH.

Methods Mol Biol. 2004;256:21-37. No abstract available.

PMID:
15024157
17.

The methylated component of the Neurospora crassa genome.

Selker EU, Tountas NA, Cross SH, Margolin BS, Murphy JG, Bird AP, Freitag M.

Nature. 2003 Apr 24;422(6934):893-7.

PMID:
12712205
18.

Identification and characterization of a novel murine beta-defensin-related gene.

Morrison GM, Rolfe M, Kilanowski FM, Cross SH, Dorin JR.

Mamm Genome. 2002 Aug;13(8):445-51. Erratum in: Mamm Genome. 2002 Oct;13(10):603.

PMID:
12226710
19.

Isolation of CpG islands using a methyl-CpG binding column.

Cross SH.

Methods Mol Biol. 2002;200:111-30. No abstract available.

PMID:
11951647
20.

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Thaung C, West K, Clark BJ, McKie L, Morgan JE, Arnold K, Nolan PM, Peters J, Hunter AJ, Brown SD, Jackson IJ, Cross SH.

Hum Mol Genet. 2002 Apr 1;11(7):755-67.

PMID:
11929848
21.

CpG island libraries from human chromosomes 18 and 22: landmarks for novel genes.

Cross SH, Clark VH, Simmen MW, Bickmore WA, Maroon H, Langford CF, Carter NP, Bird AP.

Mamm Genome. 2000 May;11(5):373-83.

PMID:
10790537
22.

Isolation of CpG islands from large genomic clones.

Cross SH, Clark VH, Bird AP.

Nucleic Acids Res. 1999 May 15;27(10):2099-107.

23.

12th International Mouse Genome Conference.

Manolakou K, Cross SH, Simpson EH, Jackson IJ.

Genomics. 1999 Apr 1;57(1):184-8. No abstract available.

PMID:
10191104
24.
25.

The chromosomal distribution of CpG islands in the mouse: evidence for genome scrambling in the rodent lineage.

Cross SH, Lee M, Clark VH, Craig JM, Bird AP, Bickmore WA.

Genomics. 1997 Mar 15;40(3):454-61.

PMID:
9073513
26.

CpG islands of chicken are concentrated on microchromosomes.

McQueen HA, Fantes J, Cross SH, Clark VH, Archibald AL, Bird AP.

Nat Genet. 1996 Mar;12(3):321-4.

PMID:
8589727
27.

CpG islands and genes.

Cross SH, Bird AP.

Curr Opin Genet Dev. 1995 Jun;5(3):309-14. Review.

PMID:
7549424
28.

Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

Quaderi NA, Meehan RR, Tate PH, Cross SH, Bird AP, Chatterjee A, Herman GE, Brown SD.

Genomics. 1994 Aug;22(3):648-51.

PMID:
8001979
29.

Purification of CpG islands using a methylated DNA binding column.

Cross SH, Charlton JA, Nan X, Bird AP.

Nat Genet. 1994 Mar;6(3):236-44.

PMID:
8012384
30.

Cloning of human telomeres by complementation in yeast.

Cross SH, Allshire RC, McKay SJ, McGill NI, Cooke HJ.

Nature. 1989 Apr 27;338(6218):771-4.

PMID:
2541341
31.

Telomeric repeat from T. thermophila cross hybridizes with human telomeres.

Allshire RC, Gosden JR, Cross SH, Cranston G, Rout D, Sugawara N, Szostak JW, Fantes PA, Hastie ND.

Nature. 1988 Apr 14;332(6165):656-9.

PMID:
2833706
32.

A cosmid vector for systematic chromosome walking.

Cross SH, Little PF.

Gene. 1986;49(1):9-22.

PMID:
3552884
33.

A cosmid vector that facilitates restriction enzyme mapping.

Little PF, Cross SH.

Proc Natl Acad Sci U S A. 1985 May;82(10):3159-63.

34.

Disruption and facilitation of cue discrimination in the rat by cholinergic agents.

Rick JT, Whittle KL, Cross SH.

Neuropharmacology. 1981 Aug;20(8):747-52. No abstract available.

PMID:
7279146

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