Cargando…

Previously Identified Genetic Variants in ADGRL3 Are not Associated with Risk for Equine Degenerative Myeloencephalopathy across Breeds

Equine neuroaxonal dystrophy/equine degenerative myeloencephalopathy (eNAD/EDM) is a neurologic disease that has been reported in young horses from a wide range of breeds. The disease is inherited and associated with vitamin E deficiency during the first two years of life, resulting in bilateral sym...

Descripción completa

Detalles Bibliográficos
Autores principales:	Marquardt, Sabin A., Wilcox, Callie V., Burns, Erin N., Peterson, Janel A., Finno, Carrie J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2019
Materias:	Brief Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770705/ https://www.ncbi.nlm.nih.gov/pubmed/31491999 http://dx.doi.org/10.3390/genes10090681

Ejemplares similares

Equine degenerative myeloencephalopathy: prevalence, impact, and management
por: Burns, Erin N, et al.
Publicado: (2018)

Concurrent Equine Degenerative Myeloencephalopathy and Equine Motor Neuron Disease in Three Young Horses
por: Finno, C.J., et al.
Publicado: (2016)

Apparent Breed Predilection for Equid Herpesvirus-1-Associated Myeloencephalopathy (EHM) in a Multiple-Breed Herd
por: Klouth, Eva, et al.
Publicado: (2021)

Frequency of Detection of Respiratory Pathogens in Clinically Healthy Show Horses Following a Multi-County Outbreak of Equine Herpesvirus-1 Myeloencephalopathy in California
por: Wilcox, Abigail, et al.
Publicado: (2022)

TRIM39-RPP21 Variants (∆19InsCCC) Are Not Associated with Juvenile Idiopathic Epilepsy in Egyptian Arabian Horses
por: Rivas, Victor N., et al.
Publicado: (2019)

Genome‐wide association study for host genetic factors associated with equine herpesvirus type‐1 induced myeloencephalopathy
por: Dunuwille, Wangisa M. B., et al.
Publicado: (2020)

Genome-Wide Association Study and Subsequent Exclusion of ATCAY as a Candidate Gene Involved in Equine Neuroaxonal Dystrophy Using Two Animal Models
por: Hales, Erin N, et al.
Publicado: (2020)

Identification of Host Factors Associated with the Development of Equine Herpesvirus Myeloencephalopathy by Transcriptomic Analysis of Peripheral Blood Mononuclear Cells from Horses
por: Zarski, Lila M., et al.
Publicado: (2021)

Epidemiological Aspects of Equid Herpesvirus-Associated Myeloencephalopathy (EHM) Outbreaks
por: Klouth, Eva, et al.
Publicado: (2022)

Increased α‐tocopherol metabolism in horses with equine neuroaxonal dystrophy
por: Hales, Erin N., et al.
Publicado: (2021)

Nomenclature and Comparative Morphology of the Teneurin/TCAP/ADGRL Protein Families
por: Sita, Luciane V., et al.
Publicado: (2019)

Breed Distribution of SOD1 Alleles Previously Associated with Canine Degenerative Myelopathy
por: Zeng, R., et al.
Publicado: (2014)

ADGRL3 (LPHN3) variants predict substance use disorder
por: Arcos-Burgos, Mauricio, et al.
Publicado: (2019)

Lipid peroxidation biomarkers for evaluating oxidative stress in equine neuroaxonal dystrophy
por: Finno, Carrie J., et al.
Publicado: (2018)

Successful ATAC-Seq From Snap-Frozen Equine Tissues
por: Peng, Sichong, et al.
Publicado: (2021)

A Comprehensive Mutagenesis Screen of the Adhesion GPCR Latrophilin-1/ADGRL1
por: Nazarko, Olha, et al.
Publicado: (2018)

Low prevalence of equine coronavirus in foals in the largest thoroughbred horse breeding region of Japan, 2012–2014
por: Nemoto, Manabu, et al.
Publicado: (2015)

A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred foals
por: Rivas, Victor N., et al.
Publicado: (2020)

A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis
por: Vezain, Myriam, et al.
Publicado: (2018)

ADGRL3 (LPHN3) variants are associated with a refined phenotype of ADHD in the MTA study
por: Acosta, Maria T., et al.
Publicado: (2016)

G12/13 is activated by acute tethered agonist exposure in the adhesion GPCR ADGRL3
por: Mathiasen, Signe, et al.
Publicado: (2020)

Disentangling autoproteolytic cleavage from tethered agonist–dependent activation of the adhesion receptor ADGRL3
por: Perry-Hauser, Nicole A., et al.
Publicado: (2022)

Impact of alpha‐tocopherol deficiency and supplementation on sacrocaudalis and gluteal muscle fiber histopathology and morphology in horses
por: Bookbinder, Lauren, et al.
Publicado: (2019)

Proteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and altered cysteine metabolic pathways
por: Valberg, Stephanie J., et al.
Publicado: (2018)

Decoding the Equine Genome: Lessons from ENCODE
por: Peng, Sichong, et al.
Publicado: (2021)

Brain structural and functional substrates of ADGRL3 (latrophilin 3) haplotype in attention-deficit/hyperactivity disorder
por: Moreno-Alcázar, Ana, et al.
Publicado: (2021)

ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP
por: Vidal, Oscar M., et al.
Publicado: (2022)

Isoform- and ligand-specific modulation of the adhesion GPCR ADGRL3/Latrophilin3 by a synthetic binder
por: Kordon, Szymon P., et al.
Publicado: (2023)

Novel non-stimulants rescue hyperactive phenotype in an adgrl3.1 mutant zebrafish model of ADHD
por: Sveinsdóttir, Hildur Sóley, et al.
Publicado: (2022)

Efficacy of the oral supplement, Equine Omega Complete, for the prevention of gastric ulcers and alpha‐tocopherol supplementation in horses
por: Williams Louie, Elizabeth, et al.
Publicado: (2023)

Functionally Annotating Regulatory Elements in the Equine Genome Using Histone Mark ChIP-Seq
por: Kingsley, N. B., et al.
Publicado: (2019)

Equine post-breeding endometritis: A review
por: Maischberger, E, et al.
Publicado: (2008)

Regenerative Therapies for Equine Degenerative Joint Disease: A Preliminary Study
por: Broeckx, Sarah, et al.
Publicado: (2014)

Dynamics of the Equine Placental DNA Methylome and Transcriptome from Mid- to Late Gestation
por: Orellana-Guerrero, Daniela, et al.
Publicado: (2023)

Bone formation transcripts dominate the differential gene expression profile in an equine osteoporotic condition associated with pulmonary silicosis
por: Zavodovskaya, Regina, et al.
Publicado: (2018)

ADGRL3, FGF1 and DRD4: Linkage and Association with Working Memory and Perceptual Organization Candidate Endophenotypes in ADHD
por: Cervantes-Henriquez, Martha L., et al.
Publicado: (2021)

A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds
por: Rohdin, Cecilia, et al.
Publicado: (2015)

Comparison of Poly-A(+) Selection and rRNA Depletion in Detection of lncRNA in Two Equine Tissues Using RNA-seq
por: Dahlgren, Anna R., et al.
Publicado: (2020)

Developmental vascular remodeling defects and postnatal kidney failure in mice lacking Gpr116 (Adgrf5) and Eltd1 (Adgrl4)
por: Lu, Shun, et al.
Publicado: (2017)

ADGRL4/ELTD1 Silencing in Endothelial Cells Induces ACLY and SLC25A1 and Alters the Cellular Metabolic Profile
por: Favara, David M., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_b3fqu1tm9mabdmnj5jh9jdqqhk