A roadmap of the mouse genome

PP2A catalytic subunit alpha is critically required for CD8+ T-cell homeostasis and antibacterial responses.

European journal of immunology·2024

Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometry.

Communications biology·2024

Culture-Free Whole Genome Sequencing of Mycobacterium tuberculosis Using Ligand-Mediated Bead Enrichment Method.

Open forum infectious diseases·2024

Multicolumn Nanoflow Liquid Chromatography with Accelerated Offline Gradient Generation for Robust and Sensitive Single-Cell Proteome Profiling.

Analytical chemistry·2024

Metabolome-wide association identifies altered metabolites and metabolic pathways in the serum of patients with cholangiocarcinoma.

JHEP reports : innovation in hepatology·2024

Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications.

Movement disorders : official journal of the Movement Disorder Society·2024

Olduvai domains: humanity's lucky brake.

Trends in genetics : TIG·2026

Transcription in check at DNA double-strand breaks.

Trends in genetics : TIG·2026

Beyond gene expression: Single-cell transcriptomics at isoform resolution.

Trends in genetics : TIG·2026

Coordinated pre-mRNA processing at the single-transcript level.

Trends in genetics : TIG·2026

Reading another hidden message in the genetic code.

Trends in genetics : TIG·2026

The future of marsupial gene editing: What's in the (tool) pouch?

Trends in genetics : TIG·2026

Genetic Susceptibility to Nephrolithiasis: A Genome-Phenome Approach with Polygenic Risk Score Analysis.

Kidney diseases (Basel, Switzerland)·2026

Germline Variants in Centromere Binding Protein 126 Predispose to Glioblastoma.

medRxiv : the preprint server for health sciences·2026

Association Between Rare Germline Variants in Cancer Susceptibility Genes and Lung Cancer Risk.

The Annals of thoracic surgery·2026

Integrating Optical Genome Mapping into the Genetic Diagnostic Algorithm: Clinical Utility in Unresolved Autosomal Recessive Disorders from a Large Cohort.

Cytogenetic and genome research·2026

An improved SMS p.Gly56Ser mouse model of Snyder-Robinson syndrome reveals phenotypic parallels with clinical features.

Disease models & mechanisms·2026

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

European journal of human genetics : EJHG·2026

Related Experiment Videos

A roadmap of the mouse genome

Related Concept Videos

PP2A catalytic subunit alpha is critically required for CD8+ T-cell homeostasis and antibacterial responses.

Diversity of post-translational modifications and cell signaling revealed by single cell and single organelle mass spectrometry.

Culture-Free Whole Genome Sequencing of Mycobacterium tuberculosis Using Ligand-Mediated Bead Enrichment Method.

Multicolumn Nanoflow Liquid Chromatography with Accelerated Offline Gradient Generation for Robust and Sensitive Single-Cell Proteome Profiling.

Metabolome-wide association identifies altered metabolites and metabolic pathways in the serum of patients with cholangiocarcinoma.

Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications.

Olduvai domains: humanity's lucky brake.

Transcription in check at DNA double-strand breaks.

Beyond gene expression: Single-cell transcriptomics at isoform resolution.

Coordinated pre-mRNA processing at the single-transcript level.

Reading another hidden message in the genetic code.

The future of marsupial gene editing: What's in the (tool) pouch?

Genetic Susceptibility to Nephrolithiasis: A Genome-Phenome Approach with Polygenic Risk Score Analysis.

Germline Variants in Centromere Binding Protein 126 Predispose to Glioblastoma.

Association Between Rare Germline Variants in Cancer Susceptibility Genes and Lung Cancer Risk.

Integrating Optical Genome Mapping into the Genetic Diagnostic Algorithm: Clinical Utility in Unresolved Autosomal Recessive Disorders from a Large Cohort.

An improved SMS p.Gly56Ser mouse model of Snyder-Robinson syndrome reveals phenotypic parallels with clinical features.

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

Related Experiment Videos

A roadmap of the mouse genome

Related Concept Videos

Related Articles