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Preliminary investigation of potential links between pigmentation variants and opioid analgesic effectiveness in horses during cerebrospinal fluid centesis.
- Published in:
- BMC Veterinary Research, 2024, v. 20, n. 1, p. 1, doi. 10.1186/s12917-024-04139-z
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- Article
Additional evidence supports GRM6 p.Thr178Met as a cause of congenital stationary night blindness in three horse breeds.
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- Veterinary Ophthalmology, 2024, v. 27, n. 3, p. 248, doi. 10.1111/vop.13151
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- Article
Delayed embryonic development or a long sperm survival in two mares—A registration conundrum.
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- Equine Veterinary Journal, 2024, v. 56, n. 1, p. 131, doi. 10.1111/evj.13936
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- Article
Functional Annotation of the Equine Genome: from Sample Collection to Fair Data.
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- Journal of Animal Science, 2023, v. 101, p. 25, doi. 10.1093/jas/skad341.028
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- Article
The localization of centromere protein A is conserved among tissues.
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- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-05335-7
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- Article
Risk factors for insidious uveitis in the Knabstrupper breed.
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- Equine Veterinary Journal, 2023, v. 55, n. 5, p. 820, doi. 10.1111/evj.13879
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- Article
Novel genetic variant associated with globoid cell leukodystrophy in a family of mixed breed dogs.
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- Journal of Veterinary Internal Medicine, 2023, v. 37, n. 5, p. 1710, doi. 10.1111/jvim.16822
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- Article
Prevalence of the RAPGEF5 c.2624C>A and PLOD1 c.2032G>A variants associated with equine familial isolated hypoparathyroidism and fragile foal syndrome in the US Thoroughbred population (1988–2019).
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- Equine Veterinary Journal, 2023, v. 55, n. 4, p. 666, doi. 10.1111/evj.13883
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- Article
Functional annotation of the animal genomes: An integrated annotation resource for the horse.
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- PLoS Genetics, 2023, v. 18, n. 3, p. 1, doi. 10.1371/journal.pgen.1010468
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- Article
Melanocortin‐1 receptor influence in equine opioid sensitivity.
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- Equine Veterinary Education, 2023, v. 35, n. 3, p. 152, doi. 10.1111/eve.13661
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- Article
A review of investigated risk factors for developing equine recurrent uveitis.
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- Veterinary Ophthalmology, 2023, v. 26, n. 2, p. 86, doi. 10.1111/vop.13002
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- Article
Heritability of insidious uveitis in Appaloosa horses.
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- Animal Genetics, 2022, v. 53, n. 6, p. 872, doi. 10.1111/age.13267
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- Article
First reported case of fragile foal syndrome type 1 in the Thoroughbred caused by PLOD1 c.2032G>A.
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- Equine Veterinary Journal, 2022, v. 54, n. 6, p. 1086, doi. 10.1111/evj.13547
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- Article
Breed Distribution and Allele Frequencies of Base Coat Color, Dilution, and White Patterning Variants across 28 Horse Breeds.
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- Genes, 2022, v. 13, n. 9, p. 1641, doi. 10.3390/genes13091641
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- Article
A de novo missense mutation in KIT is responsible for dominant white spotting phenotype in a Standardbred horse.
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- Animal Genetics, 2022, v. 53, n. 4, p. 534, doi. 10.1111/age.13222
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- Article
A genetic investigation of equine recurrent uveitis in the Icelandic horse breed.
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- Animal Genetics, 2022, v. 53, n. 3, p. 436, doi. 10.1111/age.13200
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- Article
Analysis of Genetic Diversity in the American Standardbred Horse Utilizing Short Tandem Repeats and Single Nucleotide Polymorphisms.
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- Journal of Heredity, 2022, v. 113, n. 3, p. 238, doi. 10.1093/jhered/esab070
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- Article
Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse‐related breeds with the MYH1<sup>E321G</sup> mutation.
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- Journal of Veterinary Internal Medicine, 2022, v. 36, n. 3, p. 1152, doi. 10.1111/jvim.16417
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- Article
DNA methylation aging and transcriptomic studies in horses.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27754-y
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- Article
Identification of W13 in the American Miniature Horse and Shetland Pony Populations.
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- Genes, 2021, v. 12, n. 12, p. 1985, doi. 10.3390/genes12121985
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- Article
Response to comments on 'Whole‐genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse'.
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- Equine Veterinary Journal, 2021, v. 53, n. 6, p. 1297, doi. 10.1111/evj.13503
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- Article
Decoding the Equine Genome: Lessons from ENCODE.
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- Genes, 2021, v. 12, n. 11, p. 1707, doi. 10.3390/genes12111707
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- Article
Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats (Felis catus).
- Published in:
- Animal Genetics, 2021, v. 52, n. 3, p. 321, doi. 10.1111/age.13059
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- Article
"Adopt-a-Tissue" Initiative Advances Efforts to Identify Tissue-Specific Histone Marks in the Mare.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.649959
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- Article
Generation of a Biobank From Two Adult Thoroughbred Stallions for the Functional Annotation of Animal Genomes Initiative.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.650305
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- Article
Whole‐genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse.
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- Equine Veterinary Journal, 2021, v. 53, n. 2, p. 316, doi. 10.1111/evj.13318
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- Article
DDB2 Genetic Risk Factor for Ocular Squamous Cell Carcinoma Identified in Three Additional Horse Breeds.
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- Genes, 2020, v. 11, n. 12, p. 1460, doi. 10.3390/genes11121460
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- Article
Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States.
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- Genes, 2020, v. 11, n. 12, p. 1518, doi. 10.3390/genes11121518
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- Article
Evidence supports white spotting in donkeys as a homozygous lethal condition.
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- Animal Genetics, 2020, v. 51, n. 5, p. 840, doi. 10.1111/age.12983
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- Article
Novel Complex Unbalanced Dicentric X-Autosome Rearrangement in a Thoroughbred Mare with a Mild Effect on the Phenotype.
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- Cytogenetic & Genome Research, 2020, v. 160, n. 10, p. 597, doi. 10.1159/000511236
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- Article
Article Comparison of Poly-A<sup>+</sup> Selection and rRNA Depletion in Detection of lncRNA in Two Equine Tissues Using RNA-seq.
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- Non-Coding RNA, 2020, v. 6, n. 3, p. 1, doi. 10.3390/ncrna6030032
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- Article
A De Novo MITF Deletion Explains a Novel Splashed White Phenotype in an American Paint Horse.
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- Journal of Heredity, 2020, v. 111, n. 3, p. 287, doi. 10.1093/jhered/esaa009
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- Article
Risk factors for equine recurrent uveitis in a population of Appaloosa horses in western Canada.
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- Veterinary Ophthalmology, 2020, v. 23, n. 3, p. 515, doi. 10.1111/vop.12749
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- Article
Functionally Annotating Regulatory Elements in the Equine Genome Using Histone Mark ChIP-Seq.
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- Genes, 2020, v. 11, n. 1, p. 3, doi. 10.3390/genes11010003
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- Article
Horses with equine recurrent uveitis have an activated CD4+ T‐cell phenotype that can be modulated by mesenchymal stem cells in vitro.
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- Veterinary Ophthalmology, 2020, v. 23, n. 1, p. 160, doi. 10.1111/vop.12704
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- Article
Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies.
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- Genes, 2019, v. 10, n. 10, p. 826, doi. 10.3390/genes10100826
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- Article
Additional Evidence for DDB2 T338M as a Genetic Risk Factor for Ocular Squamous Cell Carcinoma in Horses.
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- International Journal of Genomics, 2019, p. 1, doi. 10.1155/2019/3610965
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- Article
Author Correction: Improved reference genome for the domestic horse increases assembly contiguity and composition.
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- 2019
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- Correction Notice
31 Building a functional annotation of the equine genome.
- Published in:
- Journal of Animal Science, 2019, v. 97, p. 16, doi. 10.1093/jas/skz122.030
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- Article
Limbal squamous cell carcinoma in a Rocky Mountain Horse: Case report and investigation of genetic contribution.
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- 2019
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- Case Study
Ruling out BGN variants as simple X‐linked causative mutations for bilateral corneal stromal loss in Friesian horses.
- Published in:
- Animal Genetics, 2018, v. 49, n. 6, p. 656, doi. 10.1111/age.12726
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- Publication type:
- Article
Improved reference genome for the domestic horse increases assembly contiguity and composition.
- Published in:
- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0199-z
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- Publication type:
- Article
Improved reference genome for the domestic horse increases assembly contiguity and composition.
- Published in:
- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0199-z
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- Publication type:
- Article
A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses.
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- International Journal of Cancer, 2017, v. 141, n. 2, p. 342, doi. 10.1002/ijc.30744
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- Article
GO- FAANG meeting: a Gathering On Functional Annotation of Animal Genomes.
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- Animal Genetics, 2016, v. 47, n. 5, p. 528, doi. 10.1111/age.12466
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- Article
Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness.
- Published in:
- BMC Veterinary Research, 2016, v. 12, p. 1, doi. 10.1186/s12917-016-0745-1
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- Article
Limbal squamous cell carcinoma in Haflinger horses.
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- Veterinary Ophthalmology, 2015, v. 18, n. 5, p. 404, doi. 10.1111/vop.12229
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- Publication type:
- Article
Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.
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- Animal Genetics, 2013, v. 44, n. 6, p. 763, doi. 10.1111/age.12057
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- Article
Evidence for a Retroviral Insertion in <i>TRPM1</i> as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0078280
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- Article
Accumulating Mutations in Series of Haplotypes at the <i>KIT</i> and <i>MITF</i> Loci Are Major Determinants of White Markings in Franches-Montagnes Horses.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0075071
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- Article