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A new Finnish flavor of feline coat coloration, "salmiak," is associated with a 95‐kb deletion downstream of the KIT gene.
- Published in:
- Animal Genetics, 2024, v. 55, n. 4, p. 676, doi. 10.1111/age.13438
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- Article
Idiopathic Epilepsy Risk Allele Trends in Belgian Tervuren: A Longitudinal Genetic Analysis.
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- Genes, 2024, v. 15, n. 1, p. 114, doi. 10.3390/genes15010114
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- Article
A frameshift deletion in F8 associated with hemophilia A in Labrador Retriever dogs.
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- Animal Genetics, 2023, v. 54, n. 5, p. 606, doi. 10.1111/age.13345
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- Article
A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia.
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- Human Genetics, 2023, v. 142, n. 8, p. 1221, doi. 10.1007/s00439-023-02571-z
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- Article
Multiple Origins and Genomic Basis of Complex Traits in Sighthounds.
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- Molecular Biology & Evolution, 2023, v. 40, n. 8, p. 1, doi. 10.1093/molbev/msad158
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- Article
Bayesian mixed model analysis uncovered 21 risk loci for chronic kidney disease in boxer dogs.
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- PLoS Genetics, 2023, v. 18, n. 1, p. 1, doi. 10.1371/journal.pgen.1010599
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- Article
Validation of a Chromosome 14 Risk Haplotype for Idiopathic Epilepsy in the Belgian Shepherd Dog Found to Be Associated with an Insertion in the RAPGEF5 Gene.
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- Genes, 2022, v. 13, n. 7, p. 1124, doi. 10.3390/genes13071124
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- Article
Canine DVL2 variant contributes to brachycephalic phenotype and caudal vertebral anomalies.
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- Human Genetics, 2021, v. 140, n. 11, p. 1535, doi. 10.1007/s00439-021-02261-8
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- Article
Intronic variant in POU1F1 associated with canine pituitary dwarfism.
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- Human Genetics, 2021, v. 140, n. 11, p. 1553, doi. 10.1007/s00439-021-02259-2
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- Article
In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration.
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- Human Genetics, 2021, v. 140, n. 11, p. 1593, doi. 10.1007/s00439-021-02279-y
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- Article
Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss.
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- Human Genetics, 2021, v. 140, n. 11, p. 1611, doi. 10.1007/s00439-021-02286-z
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- Article
Whole Genome Sequencing Reveals Multiple Linked Genetic Variants on Canine Chromosome 12 Associated with Risk for Symmetrical Lupoid Onychodystrophy (SLO) in the Bearded Collie.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1265, doi. 10.3390/genes12081265
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- Article
Reliable wolf-dog hybrid detection in Europe using a reduced SNP panel developed for non-invasively collected samples.
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- BMC Genomics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12864-021-07761-5
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- Article
A hypomyelinating leukodystrophy in German Shepherd dogs.
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- Journal of Veterinary Internal Medicine, 2021, v. 35, n. 3, p. 1455, doi. 10.1111/jvim.16085
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- Article
An across-breed validation study of 46 genetic markers in canine hip dysplasia.
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- BMC Genomics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12864-021-07375-x
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- Article
Correction to: Genetic characterization of Addison's disease in Bearded Collies.
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- 2020
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- Correction Notice
Genetic characterization of Addison's disease in Bearded Collies.
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- BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-07243-0
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- Article
Genetic characterization of Addison's disease in Bearded Collies.
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- BMC Genomics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12864-020-07243-0
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- Article
Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs.
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- PLoS Genetics, 2020, v. 16, n. 3, p. 1, doi. 10.1371/journal.pgen.1008651
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- Article
A putative silencer variant in a spontaneous canine model of retinitis pigmentosa.
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- PLoS Genetics, 2020, v. 16, n. 3, p. 1, doi. 10.1371/journal.pgen.1008659
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- Article
webGQT: A Shiny Server for Genotype Query Tools for Model-Based Variant Filtering.
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- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00152
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- Article
A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE).
- Published in:
- Genes, 2020, v. 11, n. 2, p. 159, doi. 10.3390/genes11020159
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- Article
Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs.
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- Genes, 2020, v. 11, n. 2, p. 163, doi. 10.3390/genes11020163
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- Article
Genetic dissection of canine hip dysplasia phenotypes and osteoarthritis reveals three novel loci.
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- BMC Genomics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12864-019-6422-6
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- Article
Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie.
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- Genes, 2019, v. 10, n. 9, p. 635, doi. 10.3390/genes10090635
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- Article
Novel protective and risk loci in hip dysplasia in German Shepherds.
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- PLoS Genetics, 2019, v. 15, n. 7, p. 1, doi. 10.1371/journal.pgen.1008197
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- Article
Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants.
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- Human Genetics, 2019, v. 138, n. 5, p. 525, doi. 10.1007/s00439-019-01997-8
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- Article
A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions.
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- Human Genetics, 2019, v. 138, n. 5, p. 535, doi. 10.1007/s00439-019-02005-9
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- Article
A homozygous missense variant in the alkaline phosphatase gene ALPL is associated with a severe form of canine hypophosphatasia.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-37801-2
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- Article
A splice site variant in INPP5E causes diffuse cystic renal dysplasia and hepatic fibrosis in dogs.
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- PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0204073
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- Article
Author Correction: Assembly and Analysis of Unmapped Genome Sequence Reads Reveal Novel Sequence and Variation in Dogs.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30169-3
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- Article
MKLN1 splicing defect in dogs with lethal acrodermatitis.
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- PLoS Genetics, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pgen.1007264
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- Article
Toxoplasma gondii seroprevalence varies by cat breed.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184659
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- Article
Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers.
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- Skeletal Muscle, 2017, v. 7, p. 9, doi. 10.1186/s13395-017-0131-0
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- Article
Nonsense variant in COL7A1 causes recessive dystrophic epidermolysis bullosa in Central Asian Shepherd dogs.
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- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0177527
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- Article
Precision Medicine in Cats: Novel Niemann-Pick Type C1 Diagnosed by Whole-Genome Sequencing.
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- Journal of Veterinary Internal Medicine, 2017, v. 31, n. 2, p. 539, doi. 10.1111/jvim.14599
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- Article
ANLN truncation causes a familial fatal acute respiratory distress syndrome in Dalmatian dogs.
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- PLoS Genetics, 2017, v. 13, n. 2, p. 1, doi. 10.1371/journal.pgen.1006625
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- Article
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.
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- PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006037
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- Article
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 3, p. 537, doi. 10.1002/ajmg.a.36895
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- Article
Expression of Foxi3 is regulated by ectodysplasin in skin appendage placodes.
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- Developmental Dynamics, 2013, v. 242, n. 6, p. 593, doi. 10.1002/dvdy.23952
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- Article
Variation in Genes Related to Cochlear Biology Is Strongly Associated with Adult-Onset Deafness in Border Collies.
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- PLoS Genetics, 2012, v. 8, n. 9, p. 1, doi. 10.1371/journal.pgen.1002898
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- Article
A Novel GUSB Mutation in Brazilian Terriers with Severe Skeletal Abnormalities Defines the Disease as Mucopolysaccharidosis VII.
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- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040281
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- Article
Ancestral T-Box Mutation Is Present in Many, but Not All, Short-Tailed Dog Breeds.
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- Journal of Heredity, 2009, v. 100, n. 2, p. 236, doi. 10.1093/jhered/esn085
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- Article