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Results: 1 to 20 of 229

1.

A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis.

Guo J, O Brien DP, Mhlanga-Mutangadura T, Olby NJ, Taylor JF, Schnabel RD, Katz ML, Johnson GS.

BMC Vet Res. 2015 Jan 3;10(1):960. [Epub ahead of print]

2.

Acute oral Bryostatin-1 administration improves learning deficits in the APP/PS1 transgenic mouse model of Alzheimer's disease.

Schrott LM, Jackson K, Yi P, Dietz F, Johnson GS, Basting TF, Purdum G, Tyler T, Rios JD, Castor TP, Alexander JS.

Curr Alzheimer Res. 2015;12(1):22-31.

PMID:
25523423
3.

A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry.

Guo J, Johnson GS, Brown HA, Provencher ML, da Costa RC, Mhlanga-Mutangadura T, Taylor JF, Schnabel RD, O'Brien DP, Katz ML.

Mol Genet Metab. 2014 Aug;112(4):302-9. doi: 10.1016/j.ymgme.2014.05.014. Epub 2014 Jun 4.

4.

Cascaded all-optical operations in a hybrid integrated 80-Gb/s logic circuit.

LeGrange JD, Dinu M, Sochor T, Bollond P, Kasper A, Cabot S, Johnson GS, Kang I, Grant A, Kay J, Jaques J.

Opt Express. 2014 Jun 2;22(11):13600-15. doi: 10.1364/OE.22.013600.

PMID:
24921554
5.

A homozygous KCNJ10 mutation in Jack Russell Terriers and related breeds with spinocerebellar ataxia with myokymia, seizures, or both.

Gilliam D, O'Brien DP, Coates JR, Johnson GS, Johnson GC, Mhlanga-Mutangadura T, Hansen L, Taylor JF, Schnabel RD.

J Vet Intern Med. 2014 May-Jun;28(3):871-7. doi: 10.1111/jvim.12355. Epub 2014 Apr 7.

6.

Forecast of natural aquifer discharge using a data-driven, statistical approach.

Boggs KG, Van Kirk R, Johnson GS, Fairley JP.

Ground Water. 2014 Nov-Dec;52(6):853-63. doi: 10.1111/gwat.12133. Epub 2013 Nov 4.

PMID:
24571388
7.

Breed distribution of SOD1 alleles previously associated with canine degenerative myelopathy.

Zeng R, Coates JR, Johnson GC, Hansen L, Awano T, Kolicheski A, Ivansson E, Perloski M, Lindblad-Toh K, O'Brien DP, Guo J, Katz ML, Johnson GS.

J Vet Intern Med. 2014 Mar-Apr;28(2):515-21. doi: 10.1111/jvim.12317. Epub 2014 Feb 13.

8.

People United to Sustain Health (PUSH): a community-based participatory research study.

Kennedy BM, Katzmarzyk PT, Johnson WD, Johnson GS, McGee BB, Champagne CM, Harsha DW, Crawford T, Ryan DH.

Clin Transl Sci. 2014 Apr;7(2):108-14. doi: 10.1111/cts.12133. Epub 2014 Jan 9.

PMID:
24405579
9.

Commercial viability of CNS drugs: balancing the risk/reward profile.

Johnson GS.

Neurobiol Dis. 2014 Jan;61:21-4. doi: 10.1016/j.nbd.2013.10.004. Epub 2013 Oct 11. Review.

PMID:
24121113
10.

Characterization of neuronal ceroid-lipofuscinosis in 3 cats.

Chalkley MD, Armien AG, Gilliam DH, Johnson GS, Zeng R, Wünschmann A, Kovi RC, Katz ML.

Vet Pathol. 2014 Jul;51(4):796-804. doi: 10.1177/0300985813502818. Epub 2013 Sep 11.

PMID:
24026940
11.

Genome-wide association study identifies a novel canine glaucoma locus.

Ahonen SJ, Pietilä E, Mellersh CS, Tiira K, Hansen L, Johnson GS, Lohi H.

PLoS One. 2013 Aug 7;8(8):e70903. doi: 10.1371/journal.pone.0070903. eCollection 2013.

12.

Forecasting natural aquifer discharge using a numerical model and convolution.

Boggs KG, Johnson GS, Van Kirk R, Fairley JP.

Ground Water. 2014 Jul-Aug;52(4):503-13. doi: 10.1111/gwat.12096. Epub 2013 Aug 5.

PMID:
23914881
13.

GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: a potential model for Tay Sachs disease.

Sanders DN, Zeng R, Wenger DA, Johnson GS, Johnson GC, Decker JE, Katz ML, Platt SR, O'Brien DP.

Mol Genet Metab. 2013 Jan;108(1):70-5. doi: 10.1016/j.ymgme.2012.11.008. Epub 2012 Nov 27.

PMID:
23266199
14.

A L2HGDH initiator methionine codon mutation in a Yorkshire terrier with L-2-hydroxyglutaric aciduria.

Farias FH, Zeng R, Johnson GS, Shelton GD, Paquette D, O'Brien DP.

BMC Vet Res. 2012 Jul 26;8:124. doi: 10.1186/1746-6148-8-124.

15.

Transmission of hepatitis B virus associated with assisted monitoring of blood glucose at an assisted living facility in New York State.

Schaffzin JK, Southwick KL, Clement EJ, Konings F, Ganova-Raeva L, Xia G, Khudyakov Y, Johnson GS.

Am J Infect Control. 2012 Oct;40(8):726-31. doi: 10.1016/j.ajic.2011.11.002. Epub 2012 Jan 26.

PMID:
22284938
16.

Degenerative myelopathy in a Bernese Mountain Dog with a novel SOD1 missense mutation.

Wininger FA, Zeng R, Johnson GS, Katz ML, Johnson GC, Bush WW, Jarboe JM, Coates JR.

J Vet Intern Med. 2011 Sep-Oct;25(5):1166-70. doi: 10.1111/j.1939-1676.2011.0760.x. Epub 2011 Aug 16. No abstract available.

PMID:
21848967
17.

Food shopping perceptions, behaviors, and ability to purchase healthful food items in the lower Mississippi delta.

McGee BB, Johnson GS, Yadrick MK, Richardson V, Simpson PM, Gossett JM, Thornton A, Johnson C, Bogle ML.

J Nutr Educ Behav. 2011 Sep-Oct;43(5):339-48. doi: 10.1016/j.jneb.2010.10.007. Epub 2011 Jul 26.

PMID:
21795120
18.

Public health approach to detection of non-O157 Shiga toxin-producing Escherichia coli: summary of two outbreaks and laboratory procedures.

Schaffzin JK, Coronado F, Dumas NB, Root TP, Halse TA, Schoonmaker-Bopp DJ, Lurie MM, Nicholas D, Gerzonich B, Johnson GS, Wallace BJ, Musser KA.

Epidemiol Infect. 2012 Feb;140(2):283-9. doi: 10.1017/S0950268811000719. Epub 2011 May 5.

PMID:
21554779
19.

A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers.

Farias FH, Zeng R, Johnson GS, Wininger FA, Taylor JF, Schnabel RD, McKay SD, Sanders DN, Lohi H, Seppälä EH, Wade CM, Lindblad-Toh K, O'Brien DP, Katz ML.

Neurobiol Dis. 2011 Jun;42(3):468-74. doi: 10.1016/j.nbd.2011.02.009. Epub 2011 Feb 26.

PMID:
21362476
20.

A truncated retrotransposon disrupts the GRM1 coding sequence in Coton de Tulear dogs with Bandera's neonatal ataxia.

Zeng R, Farias FH, Johnson GS, McKay SD, Schnabel RD, Decker JE, Taylor JF, Mann CS, Katz ML, Johnson GC, Coates JR, O'Brien DP.

J Vet Intern Med. 2011 Mar-Apr;25(2):267-72. doi: 10.1111/j.1939-1676.2010.0666.x. Epub 2011 Jan 31.

PMID:
21281350
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