Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24

First European case of recessive early-onset muscle weakness syndrome in a Holstein calf.

Schweizer Archiv fur Tierheilkunde·2026

[Monogenic disorders and traits in Swiss suckler cows - A review].

Schweizer Archiv fur Tierheilkunde·2026

[Overview of known and new genetic defects and their prevalence in Swiss Fleckvieh cattle].

Schweizer Archiv fur Tierheilkunde·2025

[Genetic defects in Braunvieh cattle of Switzerland - an overview].

Schweizer Archiv fur Tierheilkunde·2025

[BLIRD - a new genetic disease in Holstein cattle in Switzerland].

Schweizer Archiv fur Tierheilkunde·2024

Multiple independent de novo mutations are associated with the development of schistosoma reflexum, a lethal syndrome in cattle.

Veterinary journal (London, England : 1997)·2024

ABCB1 Frameshift Deletion in Skye Terriers With Potential Pharmacogenetic Relevance.

Animal genetics·2026

Genetic Diversity and Selection Signatures of Three Indonesian Indigenous Pig Populations From Eastern Indonesia Using Whole Genome Sequencing Data.

Animal genetics·2026

Integrative Multi-Omics Analysis Identifies Candidate MicroRNA Regulatory Networks Associated With High-Altitude Adaptation in Tibetan Pigs.

Animal genetics·2026

Genome-Wide SNP Discovery and Population Genomic Characterisation in Indian Major Carp Labeo catla (Hamilton, 1822) Through Low-Depth Whole-Genome Resequencing.

Animal genetics·2026

Detection of Myoglobin Gene Polymorphism Associated With Pigeons' Growth Traits.

Animal genetics·2026

Towards a Standard Threshold for Genome Wide Significance in Dogs.

Animal genetics·2026

Gene-Corrected Human iPSC-Derived Cardiomyocytes and Skeletal Muscles Reveal Partial Dystrophin Dp427 Preservation and Cardiac Dp116 Expression in Duchenne Muscular Dystrophy Patient With a Splice-Site Mutation in Intron 68 (c.9975-1G>T).

Circulation. Genomic and precision medicine·2026

From free text to structured genomics: future-proofing cancer registries for precision oncology.

ESMO real world data and digital oncology·2026

Investigation of allele-specific expression in citrus hybrids reveals the association between siRNA-mediated de novo methylation and high expression in citrus genomes.

Horticulture research·2026

Protective IFIH1 variant reduces islet stress and dysfunction in a type 1 diabetes genetic background.

iScience·2026

A lipid metabolism-based gene signature defines diagnosis and molecular heterogeneity in diabetic nephropathy.

Iranian journal of basic medical sciences·2026

Whole Genome Sequencing of Discordant Monozygotic Twins Reveals Regulatory Variants Associated With Nonsyndromic Orofacial Clefts.

Human mutation·2026

Related Experiment Videos

Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24

Related Concept Videos

First European case of recessive early-onset muscle weakness syndrome in a Holstein calf.

[Monogenic disorders and traits in Swiss suckler cows - A review].

[Overview of known and new genetic defects and their prevalence in Swiss Fleckvieh cattle].

[Genetic defects in Braunvieh cattle of Switzerland - an overview].

[BLIRD - a new genetic disease in Holstein cattle in Switzerland].

Multiple independent de novo mutations are associated with the development of schistosoma reflexum, a lethal syndrome in cattle.

ABCB1 Frameshift Deletion in Skye Terriers With Potential Pharmacogenetic Relevance.

Genetic Diversity and Selection Signatures of Three Indonesian Indigenous Pig Populations From Eastern Indonesia Using Whole Genome Sequencing Data.

Integrative Multi-Omics Analysis Identifies Candidate MicroRNA Regulatory Networks Associated With High-Altitude Adaptation in Tibetan Pigs.

Genome-Wide SNP Discovery and Population Genomic Characterisation in Indian Major Carp Labeo catla (Hamilton, 1822) Through Low-Depth Whole-Genome Resequencing.

Detection of Myoglobin Gene Polymorphism Associated With Pigeons' Growth Traits.

Towards a Standard Threshold for Genome Wide Significance in Dogs.

Gene-Corrected Human iPSC-Derived Cardiomyocytes and Skeletal Muscles Reveal Partial Dystrophin Dp427 Preservation and Cardiac Dp116 Expression in Duchenne Muscular Dystrophy Patient With a Splice-Site Mutation in Intron 68 (c.9975-1G>T).

From free text to structured genomics: future-proofing cancer registries for precision oncology.

Investigation of allele-specific expression in citrus hybrids reveals the association between siRNA-mediated de novo methylation and high expression in citrus genomes.

Protective IFIH1 variant reduces islet stress and dysfunction in a type 1 diabetes genetic background.

A lipid metabolism-based gene signature defines diagnosis and molecular heterogeneity in diabetic nephropathy.

Whole Genome Sequencing of Discordant Monozygotic Twins Reveals Regulatory Variants Associated With Nonsyndromic Orofacial Clefts.

Related Experiment Videos

Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24

Related Concept Videos

Related Articles