Johnson GS - Search Results

1

Canine Multiple System Degeneration Associated with Sequence Variants in SERAC1.

Zeng R, Guo J, Bullock G, Johnson GS, Katz ML. Zeng R, et al. Among authors: johnson gs. Genes (Basel). 2024 Oct 25;15(11):1378. doi: 10.3390/genes15111378. Genes (Basel). 2024. PMID: 39596578 Free PMC article.

2

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. Zeng R, et al. Among authors: johnson gc, johnson gs. J Vet Intern Med. 2014 Mar-Apr;28(2):515-21. doi: 10.1111/jvim.12317. Epub 2014 Feb 13. J Vet Intern Med. 2014. PMID: 24524809 Free PMC article.

3

Novel Homozygous ADAMTS2 Variants and Associated Disease Phenotypes in Dogs with Dermatosparactic Ehlers-Danlos Syndrome.

Jaffey JA, Bullock G, Guo J, Mhlanga-Mutangadura T, O'Brien DP, Coates JR, Morrissey R, Hutchison R, Donnelly KS, Cohn LA, Katz ML, Johnson GS. Jaffey JA, et al. Among authors: johnson gs. Genes (Basel). 2022 Nov 19;13(11):2158. doi: 10.3390/genes13112158. Genes (Basel). 2022. PMID: 36421833 Free PMC article.

4

A Homozygous MAN2B1 Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency.

Bullock G, Johnson GS, Pattridge SG, Mhlanga-Mutangadura T, Guo J, Cook J, Campbell RS, Vite CH, Katz ML. Bullock G, et al. Among authors: johnson gs. Genes (Basel). 2023 Aug 31;14(9):1746. doi: 10.3390/genes14091746. Genes (Basel). 2023. PMID: 37761886 Free PMC article.

5

Homozygous CNP Mutation and Neurodegeneration in Weimaraners: Myelin Abnormalities and Accumulation of Lipofuscin-like Inclusions.

Keller SH, Johnson GS, Bullock G, Mhlanga-Mutangadura T, Schwartz M, Pattridge SG, Guo J, Kortz GD, Katz ML. Keller SH, et al. Among authors: johnson gs. Genes (Basel). 2024 Feb 15;15(2):246. doi: 10.3390/genes15020246. Genes (Basel). 2024. PMID: 38397235 Free PMC article.

6

FAN1 Deletion Variant in Basenji Dogs with Fanconi Syndrome.

Farias FHG, Mhlanga-Mutangadura T, Guo J, Hansen L, Johnson GS, Katz ML. Farias FHG, et al. Among authors: johnson gs. Genes (Basel). 2024 Nov 14;15(11):1469. doi: 10.3390/genes15111469. Genes (Basel). 2024. PMID: 39596669 Free PMC article.

7

Coding sequence and exon/intron organization of the canine CLN3 (Batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs.

Shibuya H, Liu PC, Katz ML, Siakotos AN, Nonneman DJ, Johnson GS. Shibuya H, et al. Among authors: johnson gs. J Neurosci Res. 1998 May 1;52(3):268-75. doi: 10.1002/(SICI)1097-4547(19980501)52:3<268::AID-JNR3>3.0.CO;2-B. J Neurosci Res. 1998. PMID: 9590435

8

Mouse gene knockout models for the CLN2 and CLN3 forms of ceroid lipofuscinosis.

Katz ML, Johnson GS. Katz ML, et al. Among authors: johnson gs. Eur J Paediatr Neurol. 2001;5 Suppl A:109-14. doi: 10.1053/ejpn.2000.0445. Eur J Paediatr Neurol. 2001. PMID: 11588979

9

Assessment of plasma carnitine concentrations in relation to ceroid lipofuscinosis in Tibetan Terriers.

Katz ML, Sanders DA, Sanders DN, Hansen EA, Johnson GS. Katz ML, et al. Among authors: johnson gs. Am J Vet Res. 2002 Jun;63(6):890-5. doi: 10.2460/ajvr.2002.63.890. Am J Vet Res. 2002. PMID: 12061538 Free article.

10

A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis.

Katz ML, Khan S, Awano T, Shahid SA, Siakotos AN, Johnson GS. Katz ML, et al. Among authors: johnson gs. Biochem Biophys Res Commun. 2005 Feb 11;327(2):541-7. doi: 10.1016/j.bbrc.2004.12.038. Biochem Biophys Res Commun. 2005. PMID: 15629147

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