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Items: 1 to 50 of 58

1.

Automatically identifying, counting, and describing wild animals in camera-trap images with deep learning.

Norouzzadeh MS, Nguyen A, Kosmala M, Swanson A, Palmer MS, Packer C, Clune J.

Proc Natl Acad Sci U S A. 2018 Jun 19;115(25):E5716-E5725. doi: 10.1073/pnas.1719367115. Epub 2018 Jun 5.

2.

Anatomy of STEM teaching in North American universities.

Stains M, Harshman J, Barker MK, Chasteen SV, Cole R, DeChenne-Peters SE, Eagan MK Jr, Esson JM, Knight JK, Laski FA, Levis-Fitzgerald M, Lee CJ, Lo SM, McDonnell LM, McKay TA, Michelotti N, Musgrove A, Palmer MS, Plank KM, Rodela TM, Sanders ER, Schimpf NG, Schulte PM, Smith MK, Stetzer M, Van Valkenburgh B, Vinson E, Weir LK, Wendel PJ, Wheeler LB, Young AM.

Science. 2018 Mar 30;359(6383):1468-1470. doi: 10.1126/science.aap8892. Epub 2018 Mar 29. No abstract available.

3.

Ingesting A Sports Drink Enhances Simulated Ice Hockey Performance While Reducing Perceived Effort.

Palmer MS, Heigenhauser G, Duong M, Spriet LL.

Int J Sports Med. 2017 Dec;38(14):1061-1069. doi: 10.1055/s-0043-119874. Epub 2017 Oct 18.

PMID:
29045995
4.

A 'dynamic' landscape of fear: prey responses to spatiotemporal variations in predation risk across the lunar cycle.

Palmer MS, Fieberg J, Swanson A, Kosmala M, Packer C.

Ecol Lett. 2017 Nov;20(11):1364-1373. doi: 10.1111/ele.12832. Epub 2017 Sep 12.

PMID:
28901034
5.

Mild Dehydration Does Not Influence Performance Or Skeletal Muscle Metabolism During Simulated Ice Hockey Exercise In Men.

Palmer MS, Heigenhauser GJ, Duong M, Spriet LL.

Int J Sport Nutr Exerc Metab. 2017 Apr;27(2):169-177. doi: 10.1123/ijsnem.2016-0194. Epub 2016 Oct 21.

PMID:
27768517
7.

Maintaining hydration with a carbohydrate-electrolyte solution improves performance, thermoregulation, and fatigue during an ice hockey scrimmage.

Linseman ME, Palmer MS, Sprenger HM, Spriet LL.

Appl Physiol Nutr Metab. 2014 Nov;39(11):1214-21. doi: 10.1139/apnm-2014-0091. Epub 2014 May 28.

PMID:
25061764
8.

A novel ARC gene polymorphism is associated with reduced risk of Alzheimer's disease.

Landgren S, von Otter M, Palmér MS, Zetterström C, Nilsson S, Skoog I, Gustafson DR, Minthon L, Wallin A, Andreasen N, Bogdanovic N, Marcusson J, Blennow K, Zetterberg H, Kettunen P.

J Neural Transm (Vienna). 2012 Jul;119(7):833-42. doi: 10.1007/s00702-012-0823-x. Epub 2012 May 25.

PMID:
22622366
9.

The MiPACQ clinical question answering system.

Cairns BL, Nielsen RD, Masanz JJ, Martin JH, Palmer MS, Ward WH, Savova GK.

AMIA Annu Symp Proc. 2011;2011:171-80. Epub 2011 Oct 22.

10.

Estimated fluid and sodium balance and drink preferences in elite male junior players during an ice hockey game.

Logan-Sprenger HM, Palmer MS, Spriet LL.

Appl Physiol Nutr Metab. 2011 Feb;36(1):145-52. doi: 10.1139/H10-098.

PMID:
21326389
11.

Ubiquitin carboxyl-terminal esterase L1 (UCHL1) S18Y polymorphism in patients with cataracts.

Rudolph T, Sjölander A, Palmér MS, Minthon L, Wallin A, Andreasen N, Tasa G, Juronen E, Blennow K, Zetterberg H, Zetterberg M.

Ophthalmic Genet. 2011 Jun;32(2):75-9. doi: 10.3109/13816810.2010.544360. Epub 2011 Jan 26.

12.
13.

Ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y polymorphism in Alzheimer's disease.

Zetterberg M, Sjölander A, von Otter M, Palmér MS, Landgren S, Minthon L, Wallin A, Andreasen N, Blennow K, Zetterberg H.

Mol Neurodegener. 2010 Mar 19;5:11. doi: 10.1186/1750-1326-5-11.

14.

Prolonged moderate-intensity aerobic exercise does not alter apoptotic signaling and DNA fragmentation in human skeletal muscle.

Quadrilatero J, Bombardier E, Norris SM, Talanian JL, Palmer MS, Logan HM, Tupling AR, Heigenhauser GJ, Spriet LL.

Am J Physiol Endocrinol Metab. 2010 Mar;298(3):E534-47. doi: 10.1152/ajpendo.00678.2009. Epub 2009 Dec 8.

15.

No association of VEGF polymorphims with Alzheimer's disease.

Landgren S, Palmér MS, Skoog I, Minthon L, Wallin A, Andreasen N, Zetterberg M, Blennow K, Zetterberg H.

Neuromolecular Med. 2010 Sep;12(3):224-8. doi: 10.1007/s12017-009-8096-8. Epub 2009 Oct 20.

PMID:
19842071
16.

Sweat rate, salt loss, and fluid intake during an intense on-ice practice in elite Canadian male junior hockey players.

Palmer MS, Spriet LL.

Appl Physiol Nutr Metab. 2008 Apr;33(2):263-71. doi: 10.1139/H08-011.

PMID:
18347681
17.

Association of complement factor H Y402H gene polymorphism with Alzheimer's disease.

Zetterberg M, Landgren S, Andersson ME, Palmér MS, Gustafson DR, Skoog I, Minthon L, Thelle DS, Wallin A, Bogdanovic N, Andreasen N, Blennow K, Zetterberg H.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):720-6. doi: 10.1002/ajmg.b.30668.

PMID:
18163432
18.

Methylenetetrahydrofolate reductase genetic polymorphisms in patients with primary open-angle glaucoma.

Zetterberg M, Tasa G, Palmér MS, Juronen E, Toover E, Blennow K, Zetterberg H.

Ophthalmic Genet. 2007 Jun;28(2):47-50.

PMID:
17558844
19.

Apolipoprotein E polymorphisms in patients with primary open-angle glaucoma.

Zetterberg M, Tasa G, Palmér MS, Juronen E, Teesalu P, Blennow K, Zetterberg H.

Am J Ophthalmol. 2007 Jun;143(6):1059-60.

PMID:
17524782
21.

Animation control for real-time virtual humans.

Badler NI, Palmer MS, Bindiganavale R.

Commun ACM. 1999 Aug;42(8):64-73. No abstract available.

PMID:
11543550
22.

Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online.

Palmer MS, Beck JA, Campbell TA, Humphries CB, Roques PK, Fox NC, Harvey R, Rossor MN, Collinge J.

Hum Mutat. 1999;13(3):256.

PMID:
10090481
23.

Conformational properties of the prion octa-repeat and hydrophobic sequences.

Smith CJ, Drake AF, Banfield BA, Bloomberg GB, Palmer MS, Clarke AR, Collinge J.

FEBS Lett. 1997 Apr 1;405(3):378-84.

24.

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

Windl O, Dempster M, Estibeiro JP, Lathe R, de Silva R, Esmonde T, Will R, Springbett A, Campbell TA, Sidle KC, Palmer MS, Collinge J.

Hum Genet. 1996 Sep;98(3):259-64.

PMID:
8707291
25.

A prion disease with a novel 96-base pair insertional mutation in the prion protein gene.

Campbell TA, Palmer MS, Will RG, Gibb WR, Luthert PJ, Collinge J.

Neurology. 1996 Mar;46(3):761-6.

PMID:
8618679
26.

Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies.

Palmer MS, van Leeven RH, Mahal SP, Campbell TA, Humphreys CB, Collinge J.

Hum Mutat. 1996;7(3):280-1. No abstract available.

PMID:
8829666
27.

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein.

Collinge J, Palmer MS, Sidle KC, Hill AF, Gowland I, Meads J, Asante E, Bradley R, Doey LJ, Lantos PL.

Nature. 1995 Dec 21-28;378(6559):779-83. Erratum in: Nature 1997 Oct 2;389(6650):526.

PMID:
8524411
28.

Transmission of fatal familial insomnia to laboratory animals.

Collinge J, Palmer MS, Sidle KC, Gowland I, Medori R, Ironside J, Lantos P.

Lancet. 1995 Aug 26;346(8974):569-70. No abstract available.

PMID:
7658786
29.

Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein.

Whittington MA, Sidle KC, Gowland I, Meads J, Hill AF, Palmer MS, Jefferys JG, Collinge J.

Nat Genet. 1995 Feb;9(2):197-201. Erratum in: Nat Genet 1995 Apr;9(4):451.

PMID:
7719349
30.
31.

Human prion diseases.

Collinge J, Palmer MS.

Baillieres Clin Neurol. 1994 Aug;3(2):241-7. Review. No abstract available.

PMID:
7952846
32.

Prion protein is necessary for normal synaptic function.

Collinge J, Whittington MA, Sidle KC, Smith CJ, Palmer MS, Clarke AR, Jefferys JG.

Nature. 1994 Jul 28;370(6487):295-7.

PMID:
8035877
33.

Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease.

Collinge J, Palmer MS, Sidle KC, Mahal SP, Campbell T, Brown J, Hardy J, Brun AE, Gustafson L, Bakker E, et al.

J Neurol Neurosurg Psychiatry. 1994 Jun;57(6):762. No abstract available.

34.

Molecular genetics of human prion diseases.

Collinge J, Palmer MS.

Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):371-8. Review.

PMID:
7913754
35.

The human SRY transcript.

Clépet C, Schafer AJ, Sinclair AH, Palmer MS, Lovell-Badge R, Goodfellow PN.

Hum Mol Genet. 1993 Dec;2(12):2007-12.

PMID:
8111368
36.

Prion diseases in humans and their relevance to other neurodegenerative diseases.

Collinge J, Palmer MS.

Dementia. 1993 May-Aug;4(3-4):178-85. Review.

PMID:
8401789
37.

Deletions in the prion protein gene are not associated with CJD.

Palmer MS, Mahal SP, Campbell TA, Hill AF, Sidle KC, Laplanche JL, Collinge J.

Hum Mol Genet. 1993 May;2(5):541-4.

PMID:
8100163
38.

Prion dementia.

Collinge J, Palmer MS, Rossor MN, Janota I, Lantos PL.

Lancet. 1993 Mar 6;341(8845):627; author reply 627-8. No abstract available.

PMID:
8094847
39.

Inherited prion disease (PrP lysine 200) in Britain: two case reports.

Collinge J, Palmer MS, Campbell T, Sidle KC, Carroll D, Harding A.

BMJ. 1993 Jan 30;306(6873):301-2.

40.

Mutations and polymorphisms in the prion protein gene.

Palmer MS, Collinge J.

Hum Mutat. 1993;2(3):168-73. Review.

PMID:
8364585
41.

Human prion diseases.

Palmer MS, Collinge J.

Curr Opin Neurol Neurosurg. 1992 Dec;5(6):895-901. Review.

PMID:
1467584
42.

Human prion diseases.

Palmer MS, Collinge J.

Baillieres Clin Neurol. 1992 Nov;1(3):627-51. Review. No abstract available.

PMID:
1344206
43.

Prion diseases.

Collinge J, Palmer MS.

Curr Opin Genet Dev. 1992 Jun;2(3):448-54. Review.

PMID:
1504620
44.

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease.

Palmer MS, Dryden AJ, Hughes JT, Collinge J.

Nature. 1991 Jul 25;352(6333):340-2. Erratum in: Nature 1991 Aug 8;352(6335):547.

PMID:
1677164
45.

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease.

Collinge J, Palmer MS, Dryden AJ.

Lancet. 1991 Jun 15;337(8755):1441-2.

PMID:
1675319
46.

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.

Sinclair AH, Berta P, Palmer MS, Hawkins JR, Griffiths BL, Smith MJ, Foster JW, Frischauf AM, Lovell-Badge R, Goodfellow PN.

Nature. 1990 Jul 19;346(6281):240-4.

PMID:
1695712
47.

Comparison of human ZFY and ZFX transcripts.

Palmer MS, Berta P, Sinclair AH, Pym B, Goodfellow PN.

Proc Natl Acad Sci U S A. 1990 Mar;87(5):1681-5.

48.

Human trophoblast and the choriocarcinoma cell line BeWo express a truncated HLA Class I molecule.

Ellis SA, Palmer MS, McMichael AJ.

J Immunol. 1990 Jan 15;144(2):731-5.

PMID:
2295808
49.

Mammalian sex determination.

Palmer MS.

Eur J Cancer. 1990;26(9):992-3. No abstract available.

PMID:
2149028
50.

Genetic evidence that ZFY is not the testis-determining factor.

Palmer MS, Sinclair AH, Berta P, Ellis NA, Goodfellow PN, Abbas NE, Fellous M.

Nature. 1989 Dec 21-28;342(6252):937-9.

PMID:
2594087

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