A polymorphic (TG)n microsatellite in an intron of the canine angiotensin I converting enzyme gene

Prevalence, geographic distribution, and impact on lifespan of a dilated cardiomyopathy-associated RNA-binding motif protein 20 variant in genotyped dogs.

Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology·2021

Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency in 30 dogs.

Scientific reports·2020

A homozygous ADAMTS2 nonsense mutation in a Doberman Pinscher dog with Ehlers Danlos syndrome and extreme skin fragility.

Animal genetics·2019

Long-term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency.

Journal of veterinary internal medicine·2017

GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB.

Journal of veterinary internal medicine·2017

Homozygous PPT1 Splice Donor Mutation in a Cane Corso Dog With Neuronal Ceroid Lipofuscinosis.

Journal of veterinary internal medicine·2016

The Chromosomal Organization of Isleria hauxwelli and Its Meaning for the Karyotypic Evolution in Thamnophilidae (Passeriformes).

Animal genetics·2026

Mitogenome Insights Into the Domestication and Phylogeography of Zebu Cattle: A Focus on Pakistani Breeds and Asian Lineages.

Animal genetics·2026

Weighted Single-Step GWAS Reveals Genetic Mechanisms Underlying Pregnancy Loss in Early Nellore Heifers.

Animal genetics·2026

Implementation of Metafounders in the Genomic Prediction for the Polled Trait in Brahman Cattle Using a Multi-Breed Population.

Animal genetics·2026

FBLN1 Regulates Embryonic Myoblast Proliferation and Differentiation in Geese: Functional Characterization of a Meat Quality-Associated Candidate Gene From Prior Multi-Omics Screening.

Animal genetics·2026

ABCB1 Frameshift Deletion in Skye Terriers With Potential Pharmacogenetic Relevance.

Animal genetics·2026

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

Prenatal diagnosis·2026

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

Experimental biology and medicine (Maywood, N.J.)·2026

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

medRxiv : the preprint server for health sciences·2026

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Molecular genetics and genomics : MGG·2026

Related Experiment Videos

A polymorphic (TG)n microsatellite in an intron of the canine angiotensin I converting enzyme gene

Related Concept Videos

Prevalence, geographic distribution, and impact on lifespan of a dilated cardiomyopathy-associated RNA-binding motif protein 20 variant in genotyped dogs.

Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency in 30 dogs.

A homozygous ADAMTS2 nonsense mutation in a Doberman Pinscher dog with Ehlers Danlos syndrome and extreme skin fragility.

Long-term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency.

GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB.

Homozygous PPT1 Splice Donor Mutation in a Cane Corso Dog With Neuronal Ceroid Lipofuscinosis.

The Chromosomal Organization of Isleria hauxwelli and Its Meaning for the Karyotypic Evolution in Thamnophilidae (Passeriformes).

Mitogenome Insights Into the Domestication and Phylogeography of Zebu Cattle: A Focus on Pakistani Breeds and Asian Lineages.

Weighted Single-Step GWAS Reveals Genetic Mechanisms Underlying Pregnancy Loss in Early Nellore Heifers.

Implementation of Metafounders in the Genomic Prediction for the Polled Trait in Brahman Cattle Using a Multi-Breed Population.

FBLN1 Regulates Embryonic Myoblast Proliferation and Differentiation in Geese: Functional Characterization of a Meat Quality-Associated Candidate Gene From Prior Multi-Omics Screening.

ABCB1 Frameshift Deletion in Skye Terriers With Potential Pharmacogenetic Relevance.

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

Related Experiment Videos

A polymorphic (TG)n microsatellite in an intron of the canine angiotensin I converting enzyme gene

Related Concept Videos

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