Presumptive translocation type trisomy in embryos sired by bulls heterozygous for the 1/29 translocation

Prognostic and predictive capacity of tumor infiltrating lymphocytes in the MA.20 regional node radiotherapy trial.

NPJ breast cancer·2025

Effects of EGF and melatonin on gene expression of cumulus cells and further in vitro embryo development in bovines.

Zygote (Cambridge, England)·2022

The effect of renin-angiotensin-aldosterone system blockers on the progression of chronic kidney disease in hypertensive elderly patients without proteinuria: PROERCAN study. Rationale and design.

Hipertension y riesgo vascular·2020

Synaptonemal Complex Analysis of Spermatocytes in Hybrids of Silver Fox and Blue Fox.

The Journal of heredity·2019

Thyroid hormone receptor beta-1 expression in early breast cancer: a validation study.

Breast cancer research and treatment·2018

Expansion of a CD26low Effector TH Subset and Reduction in Circulating Levels of sCD26 in Stable Allergic Asthma in Adults.

Journal of investigational allergology & clinical immunology·2018

LncRNA FBXL19-AS1 regulates the miR-650/ITGB3 axis to drive pathological progression in Alzheimer's Disease.

Hereditas·2026

Esketamine induces ferroptosis and suppresses immune evasion in lung adenocarcinoma cells via the hsa_circ_0022392/miR-548b-3p/MAP7 axis.

Hereditas·2026

Preliminary functional characterization of the LMNA c.929 A > G (p.Gln310Arg) variant identified in a patient with dilated cardiomyopathy.

Hereditas·2026

LncRNA RASAL2-AS1 serves as a potential biomarker for prognosis and regulates cellular processes via the miR-590-5p/PDCD5 axis and Wnt/β-catenin pathway in cervical cancer.

Hereditas·2026

Hypoxia-activated DLL4/NOTCH-EDN1 signaling maintains fibroblast activation and endothelial crosstalk in a human dermal fibroblast model of keloid-like remodeling.

Hereditas·2026

The diagnostic value of miR-4281 for knee osteoarthritis and its mechanism of action on the extracellular matrix of chondrocytes and apoptosis.

Hereditas·2026

Biobank analysis of canine eye disease variants identifies new breed associations and a potential X-linked Retinoschisin 1 disease model.

G3 (Bethesda, Md.)·2026

Whole-Exome Sequencing Identifies a Rare CSRP3 Variant Associated With Familial Brugada Syndrome in a Lebanese Family.

Journal of cardiovascular electrophysiology·2026

Genetic Variants Associated with Ventricular Septal Defect in Malaysia: A Scoping Review of Current Evidence and Research Gaps.

Pediatric cardiology·2026

Genetic Insights into the Potential Causal Role of LIPA and LTA4H in Vitiligo: A Single-Cell Integrative Analysis.

Clinical, cosmetic and investigational dermatology·2026

Genome-wide selection signatures in Ramlıç sheep identified by complementary ROH and iHS analyses.

Frontiers in veterinary science·2026

Promoter variation in BraHDAC1 modulates stomatal regulation and thermotolerance in Brassica rapa.

The Plant cell·2026

Presumptive translocation type trisomy in embryos sired by bulls heterozygous for the 1/29 translocation

Related Experiment Videos

Related Concept Videos

Prognostic and predictive capacity of tumor infiltrating lymphocytes in the MA.20 regional node radiotherapy trial.

Effects of EGF and melatonin on gene expression of cumulus cells and further in vitro embryo development in bovines.

The effect of renin-angiotensin-aldosterone system blockers on the progression of chronic kidney disease in hypertensive elderly patients without proteinuria: PROERCAN study. Rationale and design.

Synaptonemal Complex Analysis of Spermatocytes in Hybrids of Silver Fox and Blue Fox.

Thyroid hormone receptor beta-1 expression in early breast cancer: a validation study.

Expansion of a CD26low Effector TH Subset and Reduction in Circulating Levels of sCD26 in Stable Allergic Asthma in Adults.

LncRNA FBXL19-AS1 regulates the miR-650/ITGB3 axis to drive pathological progression in Alzheimer's Disease.

Esketamine induces ferroptosis and suppresses immune evasion in lung adenocarcinoma cells via the hsa_circ_0022392/miR-548b-3p/MAP7 axis.

Preliminary functional characterization of the LMNA c.929 A > G (p.Gln310Arg) variant identified in a patient with dilated cardiomyopathy.

LncRNA RASAL2-AS1 serves as a potential biomarker for prognosis and regulates cellular processes via the miR-590-5p/PDCD5 axis and Wnt/β-catenin pathway in cervical cancer.

Hypoxia-activated DLL4/NOTCH-EDN1 signaling maintains fibroblast activation and endothelial crosstalk in a human dermal fibroblast model of keloid-like remodeling.

The diagnostic value of miR-4281 for knee osteoarthritis and its mechanism of action on the extracellular matrix of chondrocytes and apoptosis.

Biobank analysis of canine eye disease variants identifies new breed associations and a potential X-linked Retinoschisin 1 disease model.

Whole-Exome Sequencing Identifies a Rare CSRP3 Variant Associated With Familial Brugada Syndrome in a Lebanese Family.

Genetic Variants Associated with Ventricular Septal Defect in Malaysia: A Scoping Review of Current Evidence and Research Gaps.

Genetic Insights into the Potential Causal Role of LIPA and LTA4H in Vitiligo: A Single-Cell Integrative Analysis.

Genome-wide selection signatures in Ramlıç sheep identified by complementary ROH and iHS analyses.

Promoter variation in BraHDAC1 modulates stomatal regulation and thermotolerance in Brassica rapa.

Presumptive translocation type trisomy in embryos sired by bulls heterozygous for the 1/29 translocation

Related Experiment Videos

Related Concept Videos

Related Articles