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Items: 36

1.

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function.

Findlay AS, Carter RN, Starbuck B, McKie L, Nováková K, Budd PS, Keighren MA, Marsh JA, Cross SH, Simon MM, Potter PK, Morton NM, Jackson IJ.

Dis Model Mech. 2018 Dec 18;11(12). pii: dmm036426. doi: 10.1242/dmm.036426.

2.

Patient, Caregiver, and Taxpayer Knowledge of Palliative Care and Views on a Model of Community-Based Palliative Care.

Boucher NA, Bull JH, Cross SH, Kirby C, Davis JK, Taylor DH Jr.

J Pain Symptom Manage. 2018 Dec;56(6):951-956. doi: 10.1016/j.jpainsymman.2018.08.007. Epub 2018 Aug 25.

PMID:
30149059
3.

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.

4.

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.

5.

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.

6.

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.

7.

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.

8.

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.

9.

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.

10.

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.

11.

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.

12.

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
13.

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.

14.

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
15.

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
16.

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
17.

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
18.

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
19.

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
20.

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
21.

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

Cross SH.

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

PMID:
11951647
22.

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
23.

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
24.

Isolation of CpG islands from large genomic clones.

Cross SH, Clark VH, Bird AP.

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

25.

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
26.
27.

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
28.

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
29.

CpG islands and genes.

Cross SH, Bird AP.

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

PMID:
7549424
30.

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
31.

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
32.

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
33.

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
34.

A cosmid vector for systematic chromosome walking.

Cross SH, Little PF.

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

PMID:
3552884
35.

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.

36.

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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