Whole blood gene expression analysis of spontaneous hypertriglyceridemia in dogs suggests an underlying pro-thrombotic process.

Authors: Baker, Lauren A.¹ (AUTHOR) lauren.a.baker@wisc.edu, Minor, Katie M.² (AUTHOR), Tate, Nicole² (AUTHOR), Furrow, Eva² (AUTHOR)

Source: PLoS ONE. 11/12/2024, Vol. 19 Issue 11, p1-14. 14p.

Subject Terms: *PLASMINOGEN activator inhibitors, *DISEASE complications, *GENE expression, *INSULIN resistance, *METABOLIC syndrome, *DOGS

Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype

Authors: Shelton, G. Diane, Minor, Katie M., Vieira, Natassia M., Kunkel, Louis M., Friedenberg, Steven G., Cullen, Jonah N., Guo, Ling T., Zatz, Mayana, Mickelson, James R.

Source: In Neuromuscular Disorders October 2022 32(10):836-841

Targeted sequencing of candidate gene regions for myelofibrosis in dogs

Authors: Campbell, Amelia G., Seelig, Davis M., Beckman, Joan D., Minor, Katie M., Heinrich, Daniel A., Friedenberg, Steven G., Modiano, Jaime F., Furrow, Eva

Source: Journal of veterinary internal medicine. 36(4):1237-1247

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Multiple variants in XDH and MOCOS underlie xanthine urolithiasis in dogs

Authors: Tate, Nicole M., Minor, Katie M., Lulich, Jody P., Mickelson, James R., Berent, Allyson, Foster, Jonathan D., Petersen, Kasey H., Furrow, Eva

Source: In Molecular Genetics and Metabolism Reports December 2021 29

Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation

Authors: Shelton, G. Diane, Minor, Katie M., Guo, Ling T., Friedenberg, Steven G., Cullen, Jonah N., Hord, Jeffrey M., Venzke, David, Anderson, Mary E., Devereaux, Megan, Prouty, Sally J., Handelman, Caryl, Campbell, Kevin P., Mickelson, James R.

Source: In Neuromuscular Disorders November 2021 31(11):1169-1178

Biliverdinuria Caused by Exonic BLVRA Deletions in Two Dogs with Green Urine.

Authors: Furrow, Eva, Peralta, Jade A., Moore, A Russell, Minor, Katie M., Guerrero, Candace, Hemmila, Charlotte R., DiCiccio, Victoria, Cullen, Jonah N., Friedenberg, Steven G., Giger, Urs

Source: Genes; Dec2024, Vol. 15 Issue 12, p1561, 13p

Subject Terms: INBORN errors of metabolism, WHOLE genome sequencing, BILIVERDIN, MASS spectrometry, MEDICAL screening

Pathogenic variants in COL6A3 cause Ullrich-like congenital muscular dystrophy in young Labrador Retriever dogs

Authors: Bolduc, Véronique, Minor, Katie M., Hu, Ying, Kaur, Rupleen, Friedenberg, Steven G., Van Buren, Samantha, Guo, Ling T., Glennon, Joseph C., Marioni-Henry, Katia, Mickelson, James R., Bönnemann, Carsten G., Shelton, G. Diane

Source: In Neuromuscular Disorders May 2020 30(5):360-367

Hereditary xanthinuria in a goat

Authors: Vail, Krystal J., Tate, Nicole M., Likavec, Tasha, Minor, Katie M., Gibbons, Philippa M., Rech, Raquel R., Furrow, Eva

Source: Journal of veterinary internal medicine. 33(2):1009-1014

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100082953398.0x000001&indx=1&recIds=ETOCvdc_100082953398.0x000001

Variants in CLCN1 and PDE4C Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs.

Authors: Shelton, G. Diane, Mickelson, James R., Friedenberg, Steven G., Cullen, Jonah N., Graham, Karina, Carpentier, Missy C., Guo, Ling T., Minor, Katie M.

Source: Animals (2076-2615); Mar2024, Vol. 14 Issue 5, p722, 12p

Subject Terms: MUSCULAR hypertrophy, ANIMAL diseases, BULLDOG, NEUROMUSCULAR diseases, NEMALINE myopathy, WHOLE genome sequencing, FACIOSCAPULOHUMERAL muscular dystrophy

A Novel CARMIL2 Immunodeficiency Identified in a Subset of Cavalier King Charles Spaniels with Pneumocystis and Bordetella Pneumonia.

Authors: Coffey, Emily L., Ma, Liang, Cissé, Ousmane H., Kovacs, Joseph A., Minor, Katie M., Sukura, Antti, Danesi, Patrizia, Friedenberg, Steven G., Cullen, Jonah N., Weissenbacher-Lang, Christiane, Nadeau, Julie C., Graham, Amber M., Granick, Martin N., Branson, Natalie K., Branson, Kyle C., Blasi, Barbara, Jacobs, Casandra M., Furrow, Eva

Source: Journal of Fungi; Mar2024, Vol. 10 Issue 3, p198, 11p

Subject Terms: PNEUMOCYSTIS pneumonia, SYMPTOMS, SKIN diseases, PRIMARY immunodeficiency diseases, IMMUNODEFICIENCY, T cells, BREEDING

Sequence Analysis of Six Candidate Genes in Miniature Schnauzers with Primary Hypertriglyceridemia.

Authors: Tate, Nicole M., Underwood, Michaela, Thomas-Hollands, Alison, Minor, Katie M., Cullen, Jonah N., Friedenberg, Steven G., Mickelson, James R., Xenoulis, Panagiotis G., Steiner, Joerg M., Furrow, Eva

Source: Genes; Feb2024, Vol. 15 Issue 2, p193, 11p

Subject Terms: SEQUENCE analysis, HYPERTRIGLYCERIDEMIA, WHOLE genome sequencing, GENES, GENE frequency

Sarcoglycan A mutation in miniature dachshund dogs causes limb-girdle muscular dystrophy 2D

Authors: Mickelson, James R., Minor, Katie M., Guo, Ling T., Friedenberg, Steven G., Cullen, Jonah N., Ciavarella, Amanda, Hambrook, Lydia E., Brenner, Karen M., Helmond, Sarah E., Marks, Stanley L., Shelton, G. Diane

Source: Skeletal muscle. 11(1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100191076970.0x000001&indx=1&recIds=ETOCvdc_100191076970.0x000001

A SACS deletion variant in Great Pyrenees dogs causes autosomal recessive neuronal degeneration.

Authors: Ekenstedt, Kari J.¹ (AUTHOR) kje0003@purdue.edu, Minor, Katie M.² (AUTHOR), Shelton, G. Diane³ (AUTHOR), Hammond, James J.⁴ (AUTHOR), Miller, Andrew D.⁵ (AUTHOR), Taylor, Susan M.⁶ (AUTHOR), Huang, Yanyun⁷ (AUTHOR), Mickelson, James R.² (AUTHOR)

Source: Human Genetics. Nov2023, Vol. 142 Issue 11, p1587-1601. 15p.

Subject Terms: *HOMOZYGOSITY, *FAMILIAL spastic paraplegia, *CENTRAL nervous system, *NEURODEGENERATION, *SINGLE nucleotide polymorphisms, *PERIPHERAL nervous system, *CELL death

Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich‐like congenital muscular dystrophy.

Authors: Jankelunas, Leanne, Murthy, Vishal D., Chen, Annie V., Minor, Katie M., Friedenberg, Steven G., Cullen, Jonah N., Guo, Ling T., Mickelson, James R., Shelton, G. Diane

Source: Journal of Veterinary Internal Medicine; Nov/Dec2023, Vol. 37 Issue 6, p2504-2509, 6p

Subject Terms: MUSCULAR dystrophy, FACIOSCAPULOHUMERAL muscular dystrophy, CEREBROSPINAL fluid examination, CONTRACTURE (Pathology), DOGS, CREATINE kinase

Genomic diversity and population structure of the Leonberger dog breed

Authors: Letko, Anna, Minor, Katie M., Jagannathan, Vidhya, Seefried, Franz R., Mickelson, James R., Oliehoek, Pieter, Drögemüller, Cord

Source: Genetics, selection, evolution. 52(1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100187108752.0x000001&indx=1&recIds=ETOCvdc_100187108752.0x000001

Correction to: Genomic diversity and population structure of the Leonberger dog breed

Authors: Letko, Anna, Minor, Katie M., Jagannathan, Vidhya, Seefried, Franz R., Mickelson, James R., Oliehoek, Pieter, Drögemüller, Cord

Source: Genetics, selection, evolution. 52(1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100187108721.0x000001&indx=1&recIds=ETOCvdc_100187108721.0x000001

Current Classification of Canine Muscular Dystrophies and Identification of New Variants.

Authors: Shelton, G. Diane¹ (AUTHOR) gshelton@health.cusd.edu, Minor, Katie M.² (AUTHOR) minork@umn.edu, Friedenberg, Steven G.³ (AUTHOR) fried255@umn.edu, Cullen, Jonah N.³ (AUTHOR) cull0084@umn.edu, Guo, Ling T.¹ (AUTHOR), Mickelson, James R.² (AUTHOR) micke001@umn.edu

Source: Genes. Aug2023, Vol. 14 Issue 8, p1557. 13p.

Subject Terms: *MUSCULAR dystrophy, *LIMB-girdle muscular dystrophy, *WHOLE genome sequencing, *FACIOSCAPULOHUMERAL muscular dystrophy, *EXTRACELLULAR matrix

Association analysis of dopamine transporter gene (SLC6A3) variants with risk for seizures and aggression in Border Collies

Authors: Van Buren, Samantha L., Oberbauer, Anita M., Minor, Katie M., Belanger, Janelle M., Furrow, Eva

Source: Animal genetics. 52(4):573-574

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122546235.0x000001&indx=1&recIds=ETOCvdc_100122546235.0x000001

A novel TYRP1 mutation associated with brown coat color in Siberian huskies

Authors: Van Buren, Samantha L., Mickelson, James R., Minor, Katie M.

Source: Animal genetics. 52(2):245-246

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122546683.0x000001&indx=1&recIds=ETOCvdc_100122546683.0x000001

Presence and impact of the exercise-induced collapse associated DNM1 mutation in Labrador retrievers and other breeds

Authors: Minor, Katie M., Patterson, Edward E., Keating, Marguerite K., Gross, Stephanie D., Ekenstedt, Kari J., Taylor, Susan M., Mickelson, James R.

Source: In The Veterinary Journal 2011 189(2):214-219