TSG101 may be the prototype of a class of dominant negative ubiquitin regulators

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology·2026

Diagnostic Value of Choroid Plexus-to-Lateral Ventricle Volume Ratio (CLVVR) in First-Trimester Screening (11-13⁺6 Weeks) for Fetal Autosomal Aneuploidies.

International journal of general medicine·2026

A novel PRPF31 variant associated with autosomal dominant retinitis pigmentosa in Japanese families.

Ophthalmic genetics·2026

Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.

Annals of human genetics·2026

Related Experiment Videos

TSG101 may be the prototype of a class of dominant negative ubiquitin regulators

Related Concept Videos

Thermodynamic selection: mechanisms and scenarios.

Ancient Systems of Sodium/Potassium Homeostasis as Predecessors of Membrane Bioenergetics.

Microbial culturomics: paradigm shift in the human gut microbiome study.

Spatial chemical distance based on atomic property fields.

The phylogenetic forest and the quest for the elusive tree of life.

Hax1 lacks BH modules and is peripherally associated to heavy membranes: implications for Omi/HtrA2 and PARL activity in the regulation of mitochondrial stress and apoptosis.

Interpreting human genetic variation at atomic resolution.

Genetic landscape of an in vivo protein interactome.

Crop legacies as genetic targets for sustainable farming systems.

Type 1 interferon perturbates clonal competition by reshaping human blood development.

Pan-genome-based resequencing of 2,320 accessions reveals structural variations and accelerates breeding advances in cultivated peanut.

All of Us diversity and scale yield context-dependent improvements in polygenic prediction.

A Genetic Risk Variant Associated With the Risk of Primary Biliary Cholangitis Is Inherited From Neanderthals.

Clinical and Genetic Analysis of Pediatric Neurodevelopmental Disorders With Complex Chromosomal Rearrangements in Two Cases.

Progressive Conduction System Disease Preceding Hypertrophy in IVS4 + 919G > A Fabry Variant: a Population-based Electrocardiographic Study.

Diagnostic Value of Choroid Plexus-to-Lateral Ventricle Volume Ratio (CLVVR) in First-Trimester Screening (11-13⁺6 Weeks) for Fetal Autosomal Aneuploidies.

A novel PRPF31 variant associated with autosomal dominant retinitis pigmentosa in Japanese families.

Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses.

Related Experiment Videos

TSG101 may be the prototype of a class of dominant negative ubiquitin regulators

Related Concept Videos

Related Articles