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Items: 35

1.

Earth's radiative imbalance from the Last Glacial Maximum to the present.

Baggenstos D, Häberli M, Schmitt J, Shackleton SA, Birner B, Severinghaus JP, Kellerhals T, Fischer H.

Proc Natl Acad Sci U S A. 2019 Jul 23;116(30):14881-14886. doi: 10.1073/pnas.1905447116. Epub 2019 Jul 8.

PMID:
31285336
2.

Power to participants: a call for person-centred HIV prevention services and research.

Pantelic M, Stegling C, Shackleton S, Restoy E.

J Int AIDS Soc. 2018 Oct;21 Suppl 7:e25167. doi: 10.1002/jia2.25167.

3.

Mean global ocean temperatures during the last glacial transition.

Bereiter B, Shackleton S, Baggenstos D, Kawamura K, Severinghaus J.

Nature. 2018 Jan 3;553(7686):39-44. doi: 10.1038/nature25152.

PMID:
29300008
4.

Recent advances in pericentriolar material organization: ordered layers and scaffolding gels.

Fry AM, Sampson J, Shak C, Shackleton S.

F1000Res. 2017 Aug 31;6:1622. doi: 10.12688/f1000research.11652.1. eCollection 2017. Review.

5.

Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells.

Gimpel P, Lee YL, Sobota RM, Calvi A, Koullourou V, Patel R, Mamchaoui K, Nédélec F, Shackleton S, Schmoranzer J, Burke B, Cadot B, Gomes ER.

Curr Biol. 2017 Oct 9;27(19):2999-3009.e9. doi: 10.1016/j.cub.2017.08.031. Epub 2017 Sep 28.

6.

Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.

Zhou C, Li C, Zhou B, Sun H, Koullourou V, Holt I, Puckelwartz MJ, Warren DT, Hayward R, Lin Z, Zhang L, Morris GE, McNally EM, Shackleton S, Rao L, Shanahan CM, Zhang Q.

Hum Mol Genet. 2017 Jun 15;26(12):2258-2276. doi: 10.1093/hmg/ddx116.

7.

Essential role of the Cdk2 activator RingoA in meiotic telomere tethering to the nuclear envelope.

Mikolcevic P, Isoda M, Shibuya H, del Barco Barrantes I, Igea A, Suja JA, Shackleton S, Watanabe Y, Nebreda AR.

Nat Commun. 2016 Mar 30;7:11084. doi: 10.1038/ncomms11084.

8.

Mitotic phosphorylation of SUN1 loosens its connection with the nuclear lamina while the LINC complex remains intact.

Patel JT, Bottrill A, Prosser SL, Jayaraman S, Straatman K, Fry AM, Shackleton S.

Nucleus. 2014 Sep-Oct;5(5):462-73. doi: 10.4161/nucl.36232.

9.

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization.

Meinke P, Mattioli E, Haque F, Antoku S, Columbaro M, Straatman KR, Worman HJ, Gundersen GG, Lattanzi G, Wehnert M, Shackleton S.

PLoS Genet. 2014 Sep 11;10(9):e1004605. doi: 10.1371/journal.pgen.1004605. eCollection 2014 Sep.

10.

Deagrarianisation and forest revegetation in a biodiversity hotspot on the Wild Coast, South Africa.

Shackleton R, Shackleton C, Shackleton S, Gambiza J.

PLoS One. 2014 Jun 11;9(2):e100463. doi: 10.1371/journal.pone.0100463. eCollection 2014.

11.

Deagrarianisation and forest revegetation in a biodiversity hotspot on the Wild Coast, South Africa.

Shackleton R, Shackleton C, Shackleton S, Gambiza J.

PLoS One. 2013 Oct 14;8(10):e76939. doi: 10.1371/journal.pone.0076939. eCollection 2013.

12.

A novel interaction between FRMD7 and CASK: evidence for a causal role in idiopathic infantile nystagmus.

Watkins RJ, Patil R, Goult BT, Thomas MG, Gottlob I, Shackleton S.

Hum Mol Genet. 2013 May 15;22(10):2105-18. doi: 10.1093/hmg/ddt060. Epub 2013 Feb 12.

13.

Nuclear envelope disease and chromatin organization.

Ellis JA, Shackleton S.

Biochem Soc Trans. 2011 Dec;39(6):1683-6. doi: 10.1042/BST20110744. Review.

PMID:
22103507
14.

The Role of FRMD7 in Idiopathic Infantile Nystagmus.

Watkins RJ, Thomas MG, Talbot CJ, Gottlob I, Shackleton S.

J Ophthalmol. 2012;2012:460956. doi: 10.1155/2012/460956. Epub 2011 Aug 29.

15.

MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy.

Sylvius N, Bonne G, Straatman K, Reddy T, Gant TW, Shackleton S.

FASEB J. 2011 Nov;25(11):3966-78. doi: 10.1096/fj.11-182915. Epub 2011 Aug 12.

PMID:
21840938
16.

Lamin A-linked progerias: is farnesylation the be all and end all?

Smallwood DT, Shackleton S.

Biochem Soc Trans. 2010 Feb;38(Pt 1):281-6. doi: 10.1042/BST0380281.

PMID:
20074075
17.

Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes.

Haque F, Mazzeo D, Patel JT, Smallwood DT, Ellis JA, Shanahan CM, Shackleton S.

J Biol Chem. 2010 Jan 29;285(5):3487-98. doi: 10.1074/jbc.M109.071910. Epub 2009 Nov 21.

18.

Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.

Mazereeuw-Hautier J, Wilson LC, Mohammed S, Smallwood D, Shackleton S, Atherton DJ, Harper JI.

Br J Dermatol. 2007 Jun;156(6):1308-14. Epub 2007 Apr 25. Review.

PMID:
17459035
19.

SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton.

Haque F, Lloyd DJ, Smallwood DT, Dent CL, Shanahan CM, Fry AM, Trembath RC, Shackleton S.

Mol Cell Biol. 2006 May;26(10):3738-51.

20.

Compound heterozygous ZMPSTE24 mutations reduce prelamin A processing and result in a severe progeroid phenotype.

Shackleton S, Smallwood DT, Clayton P, Wilson LC, Agarwal AK, Garg A, Trembath RC.

J Med Genet. 2005 Jun;42(6):e36. No abstract available.

21.

Role of two dileucine-like motifs in insulin receptor anchoring to microvilli.

Shackleton S, Hamer I, Foti M, Zumwald N, Maeder C, Carpentier JL.

J Biol Chem. 2002 Nov 15;277(46):43631-7. Epub 2002 Sep 5.

22.

A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies.

Lloyd DJ, Trembath RC, Shackleton S.

Hum Mol Genet. 2002 Apr 1;11(7):769-77.

PMID:
11929849
23.

Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophy.

Vigouroux C, Magré J, Vantyghem MC, Bourut C, Lascols O, Shackleton S, Lloyd DJ, Guerci B, Padova G, Valensi P, Grimaldi A, Piquemal R, Touraine P, Trembath RC, Capeau J.

Diabetes. 2000 Nov;49(11):1958-62.

PMID:
11078466
24.

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

Shackleton S, Lloyd DJ, Jackson SN, Evans R, Niermeijer MF, Singh BM, Schmidt H, Brabant G, Kumar S, Durrington PN, Gregory S, O'Rahilly S, Trembath RC.

Nat Genet. 2000 Feb;24(2):153-6.

PMID:
10655060
25.

A 2-amino acid insertion mutation (1243insACAAAA) in exon 7 of the CFTR gene.

Shackleton S, Harris A.

Hum Mutat. 1998;Suppl 1:S156-7. No abstract available.

PMID:
9452073
26.

A cystic fibrosis patient who is homozygous for the A559T mutation.

McDowell T, Shackleton S, Dear S, Stroobant J, Harris A.

Am J Hum Genet. 1995 Sep;57(3):734. No abstract available.

27.
28.

The stop mutation R553X in the CFTR gene results in exon skipping.

Hull J, Shackleton S, Harris A.

Genomics. 1994 Jan 15;19(2):362-4.

PMID:
7514569
29.

Identification of rare and novel mutations in the CFTR genes of CF patients in southern England.

Shackleton S, Hull J, Dear S, Seller A, Thomson A, Harris A.

Hum Mutat. 1994;3(2):141-51.

PMID:
7515303
30.

Abnormal mRNA splicing resulting from three different mutations in the CFTR gene.

Hull J, Shackleton S, Harris A.

Hum Mol Genet. 1993 Jun;2(6):689-92.

PMID:
7689009
31.

G27X: a novel mutation in exon 2 of the CF gene.

Shackleton S, Harris A.

Hum Mol Genet. 1992 Sep;1(6):445. No abstract available.

PMID:
1284531
32.

Detection of novel and rare mutations in exon 4 of the cystic fibrosis gene by SSCP.

Shackleton S, Beards F, Harris A.

Hum Mol Genet. 1992 Sep;1(6):439-40. No abstract available.

PMID:
1284529
33.

Non-occupational factors in occupational morbidity and mortality.

Shackleton S, Harrington JM.

Pol J Occup Med. 1989;2(2):105-30. Review.

PMID:
2489418
34.
35.

A comparison of two methods of measuring personal noise exposure.

Shackleton S, Piney MD.

Ann Occup Hyg. 1984;28(4):373-90. No abstract available.

PMID:
6529069

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