Sequencing of a novel cDNA and mapping to bovine chromosome 3 by single-strand conformation polymorphism (SSCP)

Implications of miRNA expression pattern in bovine oocytes and follicular fluids for developmental competence.

Theriogenology·2020

Understanding the effects of the bovine POLLED variants.

Animal genetics·2020

The genetic background of clinical mastitis in Holstein-Friesian cattle.

Animal : an international journal of animal bioscience·2019

Landscape of copy number variations in Bos taurus: individual - and inter-breed variability.

BMC genomics·2018

Evaluation of responses to vaccination of Angus cattle for four viruses that contribute to bovine respiratory disease complex.

Journal of animal science·2018

Views of diverse primary care patients on the roles of healthcare providers and staff and the influence of other variables in their weight management.

Clinical obesity·2017

Beyond the Transcriptome: The m6A Epitranscriptome in Bovine Mastitis.

Animal genetics·2026

Genome-Wide Characterization of Heterozygosity-Rich Regions in Kazakh Native Sheep Breeds.

Animal genetics·2026

Marker Prioritization With Different Fine Mapping Strategies Improves Genomic Selection Performance.

Animal genetics·2026

Population Genomic Survey of Dongliao Black and Jilin Spotted Pigs and Their Genetic Relationships With Northeastern Asian Breeds.

Animal genetics·2026

Breed Composition and Heterozygosity in Brangus and Braford Composite Cattle Breeds.

Animal genetics·2026

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

Animal genetics·2026

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations.

Journal of clinical laboratory analysis·2026

Advancing genetic pathogenicity prediction with three-dimensional proteoform-phenotype analysis.

medRxiv : the preprint server for health sciences·2026

Genetic Spectrum and Family-Based Cascade Screening in Vietnamese Families With Autosomal Dominant Polycystic Kidney Disease.

Nephrology (Carlton, Vic.)·2026

Construction of an AI-Assisted Pedigree Mapping System for Hereditary Gynecological Tumors: Algorithm Development and Pilot Validation Study.

JMIR medical informatics·2026

Characteristics of predicated pathogenic missense variants in human genes for Mendelian disorders.

Frontiers in bioinformatics·2026

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia.

BMC medical genomics·2026

Related Experiment Videos

Sequencing of a novel cDNA and mapping to bovine chromosome 3 by single-strand conformation polymorphism (SSCP)

Related Concept Videos

Implications of miRNA expression pattern in bovine oocytes and follicular fluids for developmental competence.

Understanding the effects of the bovine POLLED variants.

The genetic background of clinical mastitis in Holstein-Friesian cattle.

Landscape of copy number variations in Bos taurus: individual - and inter-breed variability.

Evaluation of responses to vaccination of Angus cattle for four viruses that contribute to bovine respiratory disease complex.

Views of diverse primary care patients on the roles of healthcare providers and staff and the influence of other variables in their weight management.

Beyond the Transcriptome: The m6A Epitranscriptome in Bovine Mastitis.

Genome-Wide Characterization of Heterozygosity-Rich Regions in Kazakh Native Sheep Breeds.

Marker Prioritization With Different Fine Mapping Strategies Improves Genomic Selection Performance.

Population Genomic Survey of Dongliao Black and Jilin Spotted Pigs and Their Genetic Relationships With Northeastern Asian Breeds.

Breed Composition and Heterozygosity in Brangus and Braford Composite Cattle Breeds.

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

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations.

Advancing genetic pathogenicity prediction with three-dimensional proteoform-phenotype analysis.

Genetic Spectrum and Family-Based Cascade Screening in Vietnamese Families With Autosomal Dominant Polycystic Kidney Disease.

Construction of an AI-Assisted Pedigree Mapping System for Hereditary Gynecological Tumors: Algorithm Development and Pilot Validation Study.

Characteristics of predicated pathogenic missense variants in human genes for Mendelian disorders.

Identification and splicing assessment of a novel homozygous CFAP65 splice-site variant associated with oligozoospermia and complete asthenozoospermia.

Related Experiment Videos

Sequencing of a novel cDNA and mapping to bovine chromosome 3 by single-strand conformation polymorphism (SSCP)

Related Concept Videos

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