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Items: 1 to 50 of 105

1.

Peroxisomal catalases from the yeasts Pichia pastoris and Kluyveromyces lactis as models for oxidative damage in higher eukaryotes.

Gómez S, Navas-Yuste S, Payne AM, Rivera W, López-Estepa M, Brangbour C, Fullà D, Juanhuix J, Fernández FJ, Vega MC.

Free Radic Biol Med. 2019 Jun 22;141:279-290. doi: 10.1016/j.freeradbiomed.2019.06.025. [Epub ahead of print]

2.

Do sensorimotor perturbations to standing balance elicit an error-related negativity?

Payne AM, Ting LH, Hajcak G.

Psychophysiology. 2019 Jul;56(7):e13359. doi: 10.1111/psyp.13359. Epub 2019 Mar 1. Review.

PMID:
30820966
3.

Twelve tips for developing and implementing curriculum in dedicated 'collaborative classrooms'.

McHugh D, Hall J, McLeod KM, Kovelowski CJ, Payne AM.

Med Teach. 2019 Jan 20:1-6. doi: 10.1080/0142159X.2018.1551992. [Epub ahead of print]

PMID:
30661425
4.

Complete Genome Sequences of 18 Paenibacillus larvae Phages from the Western United States.

Merrill BD, Fajardo CP, Hilton JA, Payne AM, Ward AT, Walker JK, Dhalai A, Imahara C, Mangohig J, Monk J, Pascacio C, Rai P, Salisbury A, Velez K, Bloomfield TJ, Buhler B, Duncan SG, Fuhriman DA, George J, Graves K, Heaton K, Hill HL, Kim M, Knabe BK, Ririe DB, Rogers SL, Stamereilers C, Stephenson MB, Usher BK, Ward CS, Withers JM, Wright CK, Breakwell DP, Grose JH, Hope S, Tsourkas PK.

Microbiol Resour Announc. 2018 Oct 4;7(13). pii: e00966-18. doi: 10.1128/MRA.00966-18. eCollection 2018 Oct.

5.

Dissociation of muscle and cortical response scaling to balance perturbation acceleration.

Payne AM, Hajcak G, Ting LH.

J Neurophysiol. 2019 Mar 1;121(3):867-880. doi: 10.1152/jn.00237.2018. Epub 2018 Dec 5.

PMID:
30517039
6.

Development and implementation of a health education station by community health nursing students.

Niemi CA, Payne AM, Bates R.

Public Health Nurs. 2018 Nov;35(6):581-586. doi: 10.1111/phn.12532. Epub 2018 Jul 10.

PMID:
29989205
7.

Complete Genome Sequences of Paenibacillus larvae Phages BN12, Dragolir, Kiel007, Leyra, Likha, Pagassa, PBL1c, and Tadhana.

Walker JK, Merrill BD, Berg JA, Dhalai A, Dingman DW, Fajardo CP, Graves K, Hill HL, Hilton JA, Imahara C, Knabe BK, Mangohig J, Monk J, Mun H, Payne AM, Salisbury A, Stamereilers C, Velez K, Ward AT, Breakwell DP, Grose JH, Hope S, Tsourkas PK.

Genome Announc. 2018 Jun 14;6(24). pii: e01602-17. doi: 10.1128/genomeA.01602-17.

8.

Physiological temperatures reduce dimerization of dengue and Zika virus recombinant envelope proteins.

Kudlacek ST, Premkumar L, Metz SW, Tripathy A, Bobkov AA, Payne AM, Graham S, Brackbill JA, Miley MJ, de Silva AM, Kuhlman B.

J Biol Chem. 2018 Jun 8;293(23):8922-8933. doi: 10.1074/jbc.RA118.002658. Epub 2018 Apr 20.

9.

Bacteriophages as an alternative to conventional antibiotic use for the prevention or treatment of Paenibacillus larvae in honeybee hives.

Brady TS, Merrill BD, Hilton JA, Payne AM, Stephenson MB, Hope S.

J Invertebr Pathol. 2017 Nov;150:94-100. doi: 10.1016/j.jip.2017.09.010. Epub 2017 Sep 14.

10.

Structural and functional characterization of a highly stable endo-β-1,4-xylanase from Fusarium oxysporum and its development as an efficient immobilized biocatalyst.

Gómez S, Payne AM, Savko M, Fox GC, Shepard WE, Fernandez FJ, Cristina Vega M.

Biotechnol Biofuels. 2016 Sep 5;9(1):191. doi: 10.1186/s13068-016-0605-z. eCollection 2016.

11.

Comparison of 3 silicone hydrogel bandage soft contact lenses for pain control after photorefractive keratectomy.

Taylor KR, Caldwell MC, Payne AM, Apsey DA, Townley JR, Reilly CD, Panday VA.

J Cataract Refract Surg. 2014 Nov;40(11):1798-804. doi: 10.1016/j.jcrs.2014.02.040. Epub 2014 Sep 10.

PMID:
25217073
12.

Caspase activation as a versatile assay platform for detection of cytotoxic bacterial toxins.

Payne AM, Zorman J, Horton M, Dubey S, ter Meulen J, Vora KA.

J Clin Microbiol. 2013 Sep;51(9):2970-6. doi: 10.1128/JCM.01161-13. Epub 2013 Jul 3.

13.

Multi-membership gene regulation in pathway based microarray analysis.

Pavlidis SP, Payne AM, Swift SM.

Algorithms Mol Biol. 2011 Sep 22;6:22. doi: 10.1186/1748-7188-6-22.

14.

Comparison of rhesus and cynomolgus macaques in a Streptococcus pyogenes infection model for vaccine evaluation.

Skinner JM, Caro-Aguilar IC, Payne AM, Indrawati L, Fontenot J, Heinrichs JH.

Microb Pathog. 2011 Jan;50(1):39-47. doi: 10.1016/j.micpath.2010.10.004. Epub 2010 Oct 28.

PMID:
21035535
15.

Increased CaVbeta1A expression with aging contributes to skeletal muscle weakness.

Taylor JR, Zheng Z, Wang ZM, Payne AM, Messi ML, Delbono O.

Aging Cell. 2009 Sep;8(5):584-94. doi: 10.1111/j.1474-9726.2009.00507.x. Epub 2009 Aug 5.

16.

Role of Ca2+, membrane excitability, and Ca2+ stores in failing muscle contraction with aging.

Payne AM, Jimenez-Moreno R, Wang ZM, Messi ML, Delbono O.

Exp Gerontol. 2009 Apr;44(4):261-73. doi: 10.1016/j.exger.2008.09.013. Epub 2008 Oct 10.

17.

Loss of skeletal muscle strength by ablation of the sarcoplasmic reticulum protein JP45.

Delbono O, Xia J, Treves S, Wang ZM, Jimenez-Moreno R, Payne AM, Messi ML, Briguet A, Schaerer F, Nishi M, Takeshima H, Zorzato F.

Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):20108-13. Epub 2007 Dec 5.

18.

Coccidia-induced mucogenesis promotes the onset of necrotic enteritis by supporting Clostridium perfringens growth.

Collier CT, Hofacre CL, Payne AM, Anderson DB, Kaiser P, Mackie RI, Gaskins HR.

Vet Immunol Immunopathol. 2008 Mar 15;122(1-2):104-15. Epub 2007 Dec 19.

PMID:
18068809
19.

Motor neuron targeting of IGF-1 attenuates age-related external Ca2+-dependent skeletal muscle contraction in senescent mice.

Payne AM, Messi ML, Zheng Z, Delbono O.

Exp Gerontol. 2007 Apr;42(4):309-19. Epub 2006 Dec 14.

20.

Motor neurone targeting of IGF-1 prevents specific force decline in ageing mouse muscle.

Payne AM, Zheng Z, Messi ML, Milligan CE, González E, Delbono O.

J Physiol. 2006 Jan 15;570(Pt 2):283-94. Epub 2005 Nov 17.

21.

External Ca(2+)-dependent excitation--contraction coupling in a population of ageing mouse skeletal muscle fibres.

Payne AM, Zheng Z, González E, Wang ZM, Messi ML, Delbono O.

J Physiol. 2004 Oct 1;560(Pt 1):137-55. Epub 2004 Aug 5.

22.

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.

Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, Bhattacharya SS, Bird AC, Kaplan J, Maumenee IH.

Arch Ophthalmol. 2004 Jul;122(7):1029-37.

PMID:
15249368
23.

Neurogenesis of excitation-contraction uncoupling in aging skeletal muscle.

Payne AM, Delbono O.

Exerc Sport Sci Rev. 2004 Jan;32(1):36-40. Review.

PMID:
14748548
24.
25.
26.

Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.

Bessant DA, Holder GE, Fitzke FW, Payne AM, Bhattacharya SS, Bird AC.

Arch Ophthalmol. 2003 Jun;121(6):793-802.

PMID:
12796249
27.

Guanylate cyclase activating proteins, guanylate cyclase and disease.

Newbold RJ, Deery EC, Payne AM, Wilkie SE, Hunt DM, Warren MJ.

Adv Exp Med Biol. 2002;514:411-38. Review.

PMID:
12596936
28.
29.

Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1.

Downes SM, Payne AM, Kelsell RE, Fitzke FW, Holder GE, Hunt DM, Moore AT, Bird AC.

Arch Ophthalmol. 2001 Nov;119(11):1667-73.

PMID:
11709018
30.

Clustering and frequency of mutations in the retinal guanylate cyclase (GUCY2D) gene in patients with dominant cone-rod dystrophies.

Payne AM, Morris AG, Downes SM, Johnson S, Bird AC, Moore AT, Bhattacharya SS, Hunt DM.

J Med Genet. 2001 Sep;38(9):611-4. No abstract available.

31.

Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy B, Payne AM, Bhattacharya SS, Mehdi SQ.

Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2225-8.

PMID:
11527934
32.

A new locus for autosomal recessive RP (RP29) mapping to chromosome 4q32-q34 in a Pakistani family.

Hameed A, Khaliq S, Ismail M, Anwar K, Mehdi SQ, Bessant D, Payne AM, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2001 Jun;42(7):1436-8.

33.

Spectrum of mutations in USH2A in British patients with Usher syndrome type II.

Leroy BP, Aragon-Martin JA, Weston MD, Bessant DA, Willis C, Webster AR, Bird AC, Kimberling WJ, Payne AM, Bhattacharya SS.

Exp Eye Res. 2001 May;72(5):503-9.

PMID:
11311042
34.

Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1.

Downes SM, Holder GE, Fitzke FW, Payne AM, Warren MJ, Bhattacharya SS, Bird AC.

Arch Ophthalmol. 2001 Jan;119(1):96-105.

PMID:
11146732
35.

Extragenic suppressors of the nimX2(cdc2) mutation of Aspergillus nidulans affect nuclear division, septation and conidiation.

McGuire SL, Roe DL, Carter BW, Carter RL, Grace SP, Hays PL, Lang GA, Mamaril JL, McElvaine AT, Payne AM, Schrader MD, Wahrle SE, Young CD.

Genetics. 2000 Dec;156(4):1573-84.

36.

Halothane genotype, pre-slaughter handling and stunning method all influence pork quality.

Channon HA, Payne AM, Warner RD.

Meat Sci. 2000 Nov;56(3):291-9.

PMID:
22062081
37.

Novel locus for autosomal recessive cone-rod dystrophy CORD8 mapping to chromosome 1q12-Q24.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy BP, Mehdi SQ, Payne AM, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3709-12.

PMID:
11053266
38.

NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies.

Bessant DA, Payne AM, Plant C, Bird AC, Swaroop A, Bhattacharya SS.

Eur J Hum Genet. 2000 Oct;8(10):783-7.

39.

Mutations in a new photoreceptor-pineal gene on 17p cause leber congenital amaurosis. Nat gen 2000;24:79-83

Sohoki MM, Browne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Mehdi SQ, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP.

Am J Ophthalmol. 2000 Jun;129(6):834-5. No abstract available.

40.

Importance of the autosomal recessive retinitis pigmentosa locus on 1q31-q32.1 (RP12) and mutation analysis of the candidate gene RGS16 (RGS-r)

Bessant DA, Payne AM, Snow BE, Antiño G, Mehdi SQ, Bird AC, Siderovski DP, Bhattacharya SS.

J Med Genet. 2000 May;37(5):384-7. No abstract available.

41.

Familial cavernous hemangioma: An expanding ocular spectrum.

Sarraf D, Payne AM, Kitchen ND, Sehmi KS, Downes SM, Bird AC.

Arch Ophthalmol. 2000 Jul;118(7):969-73.

PMID:
10900112
42.

Prevalence of AIPL1 mutations in inherited retinal degenerative disease.

Sohocki MM, Perrault I, Leroy BP, Payne AM, Dharmaraj S, Bhattacharya SS, Kaplan J, Maumenee IH, Koenekoop R, Meire FM, Birch DG, Heckenlively JR, Daiger SP.

Mol Genet Metab. 2000 Jun;70(2):142-50.

PMID:
10873396
43.

A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13.

Hameed A, Khaliq S, Ismail M, Anwar K, Ebenezer ND, Jordan T, Mehdi SQ, Payne AM, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2000 Mar;41(3):629-33.

44.

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP.

Nat Genet. 2000 Jan;24(1):79-83.

45.

Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 families.

Downes SM, Fitzke FW, Holder GE, Payne AM, Bessant DA, Bhattacharya SS, Bird AC.

Arch Ophthalmol. 1999 Oct;117(10):1373-83.

PMID:
10532447
46.

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).

den Hollander AI, ten Brink JB, de Kok YJ, van Soest S, van den Born LI, van Driel MA, van de Pol DJ, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, Heckenlively JR, Cremers FP, Bergen AA.

Nat Genet. 1999 Oct;23(2):217-21.

PMID:
10508521
47.

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies.

Payne AM, Downes SM, Bessant DA, Plant C, Moore T, Bird AC, Bhattacharya SS.

J Med Genet. 1999 Sep;36(9):691-3.

48.

Refinement of the locus for autosomal recessive Retinitis pigmentosa (RP25) linked to chromosome 6q in a family of Pakistani origin.

Khaliq S, Hameed A, Ismail M, Mehdi SQ, Bessant DA, Payne AM, Bhattacharya SS.

Am J Hum Genet. 1999 Aug;65(2):571-4. No abstract available.

49.

Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32.

Bessant DA, Anwar K, Khaliq S, Hameed A, Ismail M, Payne AM, Mehdi SQ, Bhattacharya SS.

Br J Ophthalmol. 1999 Aug;83(8):919-22.

50.

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.

Bessant DA, Payne AM, Mitton KP, Wang QL, Swain PK, Plant C, Bird AC, Zack DJ, Swaroop A, Bhattacharya SS.

Nat Genet. 1999 Apr;21(4):355-6. No abstract available.

PMID:
10192380

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