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Characterization of a Wheat Breeders' Array suitable for high-throughput SNP genotyping of global accessions of hexaploid bread wheat (Triticum aestivum).

Allen AM, Winfield MO, Burridge AJ, Downie RC, Benbow HR, Barker GL, Wilkinson PA, Coghill J, Waterfall C, Davassi A, Scopes G, Pirani A, Webster T, Brew F, Bloor C, Griffiths S, Bentley AR, Alda M, Jack P, Phillips AL, Edwards KJ.

Plant Biotechnol J. 2017 Mar;15(3):390-401. doi: 10.1111/pbi.12635. Epub 2016 Nov 23.


CerealsDB 3.0: expansion of resources and data integration.

Wilkinson PA, Winfield MO, Barker GL, Tyrrell S, Bian X, Allen AM, Burridge A, Coghill JA, Waterfall C, Caccamo M, Davey RP, Edwards KJ.

BMC Bioinformatics. 2016 Jun 24;17:256. doi: 10.1186/s12859-016-1139-x.


High-density SNP genotyping array for hexaploid wheat and its secondary and tertiary gene pool.

Winfield MO, Allen AM, Burridge AJ, Barker GL, Benbow HR, Wilkinson PA, Coghill J, Waterfall C, Davassi A, Scopes G, Pirani A, Webster T, Brew F, Bloor C, King J, West C, Griffiths S, King I, Bentley AR, Edwards KJ.

Plant Biotechnol J. 2016 May;14(5):1195-206. doi: 10.1111/pbi.12485. Epub 2015 Oct 15.


What's in the Gift? Towards a Molecular Dissection of Nuptial Feeding in a Cricket.

Pauchet Y, Wielsch N, Wilkinson PA, Sakaluk SK, SvatoŇ° A, ffrench-Constant RH, Hunt J, Heckel DG.

PLoS One. 2015 Oct 6;10(10):e0140191. doi: 10.1371/journal.pone.0140191. eCollection 2015.


Global analyses revealed age-related alterations in innate immune responses after stimulation of pathogen recognition receptors.

Metcalf TU, Cubas RA, Ghneim K, Cartwright MJ, Grevenynghe JV, Richner JM, Olagnier DP, Wilkinson PA, Cameron MJ, Park BS, Hiscott JB, Diamond MS, Wertheimer AM, Nikolich-Zugich J, Haddad EK.

Aging Cell. 2015 Jun;14(3):421-32. doi: 10.1111/acel.12320. Epub 2015 Feb 27.


CerealsDB 2.0: an integrated resource for plant breeders and scientists.

Wilkinson PA, Winfield MO, Barker GL, Allen AM, Burridge A, Coghill JA, Edwards KJ.

BMC Bioinformatics. 2012 Sep 3;13:219.


Targeted re-sequencing of the allohexaploid wheat exome.

Winfield MO, Wilkinson PA, Allen AM, Barker GL, Coghill JA, Burridge A, Hall A, Brenchley RC, D'Amore R, Hall N, Bevan MW, Richmond T, Gerhardt DJ, Jeddeloh JA, Edwards KJ.

Plant Biotechnol J. 2012 Aug;10(6):733-42. doi: 10.1111/j.1467-7652.2012.00713.x. Epub 2012 Jun 18.


Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry.

Joron M, Frezal L, Jones RT, Chamberlain NL, Lee SF, Haag CR, Whibley A, Becuwe M, Baxter SW, Ferguson L, Wilkinson PA, Salazar C, Davidson C, Clark R, Quail MA, Beasley H, Glithero R, Lloyd C, Sims S, Jones MC, Rogers J, Jiggins CD, ffrench-Constant RH.

Nature. 2011 Aug 14;477(7363):203-6. doi: 10.1038/nature10341.


Genome-wide analysis reveals loci encoding anti-macrophage factors in the human pathogen Burkholderia pseudomallei K96243.

Dowling AJ, Wilkinson PA, Holden MT, Quail MA, Bentley SD, Reger J, Waterfield NR, Titball RW, Ffrench-Constant RH.

PLoS One. 2010 Dec 22;5(12):e15693. doi: 10.1371/journal.pone.0015693.


Neuroschistosomiasis presenting as brainstem encephalitis.

Devine MJ, Wilkinson PA, Doherty JF, Jarman PR.

Neurology. 2008 Jun 3;70(23):2262-4. doi: 10.1212/01.wnl.0000313839.73358.c0. No abstract available.


Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.

Tsaousidou MK, Ouahchi K, Warner TT, Yang Y, Simpson MA, Laing NG, Wilkinson PA, Madrid RE, Patel H, Hentati F, Patton MA, Hentati A, Lamont PJ, Siddique T, Crosby AH.

Am J Hum Genet. 2008 Feb;82(2):510-5. doi: 10.1016/j.ajhg.2007.10.001. Epub 2008 Jan 18.


A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.

Reed JA, Wilkinson PA, Patel H, Simpson MA, Chatonnet A, Robay D, Patton MA, Crosby AH, Warner TT.

Neurogenetics. 2005 May;6(2):79-84. Epub 2005 Feb 12.


A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14.

Wilkinson PA, Simpson MA, Bastaki L, Patel H, Reed JA, Kalidas K, Samilchuk E, Khan R, Warner TT, Crosby AH.

J Med Genet. 2005 Jan;42(1):80-2. No abstract available.


Severe hemiplegic migraine attack precipitated by fentanyl sedation for esophagogastroscopy.

Gil-Gouveia R, Wilkinson PA, Kaube H.

Neurology. 2004 Dec 28;63(12):2446-7. Review. No abstract available.


A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia.

Wilkinson PA, Crosby AH, Turner C, Bradley LJ, Ginsberg L, Wood NW, Schapira AH, Warner TT.

Brain. 2004 May;127(Pt 5):973-80. Epub 2004 Feb 25. Erratum in: Brain. 2004 Sep;127(Pt 9):2148.


SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia.

Wilkinson PA, Hart PE, Patel H, Warner TT, Crosby AH.

J Neurol Sci. 2003 Dec 15;216(1):43-5.


A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia.

Wilkinson PA, Crosby AH, Turner C, Patel H, Wood NW, Schapira AH, Warner TT.

Neurology. 2003 Jul 22;61(2):235-8.


Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.

Proukakis C, Auer-Grumbach M, Wagner K, Wilkinson PA, Reid E, Patton MA, Warner TT, Crosby AH.

Hum Mutat. 2003 Feb;21(2):170.


Intrinsic spinal cord lesions complicating epidural anaesthesia and analgesia: report of three cases.

Wilkinson PA, Valentine A, Gibbs JM.

J Neurol Neurosurg Psychiatry. 2002 Apr;72(4):537-9.


Friedreich's ataxia presenting as an isolated spastic paraparesis.

Wilkinson PA, Bradley JL, Warner TT.

J Neurol Neurosurg Psychiatry. 2001 Nov;71(5):709. No abstract available.

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