Johnson GS - Search Results

1

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.

2

Lysosomal storage disease associated with a CNP sequence variant in Dalmatian dogs.

Bullock G, Johnson GS, Mhlanga-Mutangadura T, Petesch SC, Thompson S, Goebbels S, Katz ML. Bullock G, et al. Among authors: johnson gs. Gene. 2022 Jul 1;830:146513. doi: 10.1016/j.gene.2022.146513. Epub 2022 Apr 18. Gene. 2022. PMID: 35447247 Free 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

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.

7

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

8

Assessment of retinal function and characterization of lysosomal storage body accumulation in the retinas and brains of Tibetan Terriers with ceroid-lipofuscinosis.

Katz ML, Narfström K, Johnson GS, O'Brien DP. Katz ML, et al. Among authors: johnson gs. Am J Vet Res. 2005 Jan;66(1):67-76. doi: 10.2460/ajvr.2005.66.67. Am J Vet Res. 2005. PMID: 15691038 Free article.

9

An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.

Farias FH, Johnson GS, Taylor JF, Giuliano E, Katz ML, Sanders DN, Schnabel RD, McKay SD, Khan S, Gharahkhani P, O'Leary CA, Pettitt L, Forman OP, Boursnell M, McLaughlin B, Ahonen S, Lohi H, Hernandez-Merino E, Gould DJ, Sargan DR, Mellersh C. Farias FH, et al. Among authors: johnson gs. Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4716-21. doi: 10.1167/iovs.09-5142. Epub 2010 Apr 7. Invest Ophthalmol Vis Sci. 2010. PMID: 20375329

10

A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund.

Sanders DN, Farias FH, Johnson GS, Chiang V, Cook JR, O'Brien DP, Hofmann SL, Lu JY, Katz ML. Sanders DN, et al. Among authors: johnson gs. Mol Genet Metab. 2010 Aug;100(4):349-56. doi: 10.1016/j.ymgme.2010.04.009. Epub 2010 Apr 24. Mol Genet Metab. 2010. PMID: 20494602 Free PMC article.

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