Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

The AE4 transporter mediates kidney acid-base sensing.

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[Geminivirus replication: rolling circle mechanism in plants].

Virologie (Montrouge, France)·2022

[Nanoviruses, small plant viruses: similarities and differences with geminiviruses].

Virologie (Montrouge, France)·2021

Probabilistic tsunami forecasting for early warning.

Nature communications·2021

Relationship between intervention dosage and success of resource connections in a social needs intervention.

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Plasma levels of protein C pathway proteins and brain magnetic resonance imaging volumes in multiple sclerosis.

European journal of neurology·2019

Scalable, generalizable and uncertainty-aware integration of spatial multiomics across diverse modalities and platforms with SCIGMA.

Nature genetics·2026

Spatiotemporal lineage tracing reveals the dynamic spatial architecture of tumor growth and metastasis.

Nature genetics·2026

A single-cell atlas of multiple myeloma defines malignant archetypes and proliferative states.

Nature genetics·2026

Mechanisms and functional implications of long-range enhancer-dependent gene regulation.

Nature genetics·2026

A multiancestry polygenic risk score for Alzheimer's disease is associated with cognitive decline and neuropathological hallmarks in diverse populations.

Nature genetics·2026

Dissecting pleiotropy between major depressive disorder and physical disease comorbidities.

Nature genetics·2026

Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.

Human mutation·2026

Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.

Endocrine, metabolic & immune disorders drug targets·2026

Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.

Molecular psychiatry·2026

Methodological frameworks to probe histone acetylation-driven circuit plasticity in SYNGAP1-associated neurodevelopmental disorders.

Methods in enzymology·2026

Exploring the genetic spectrum of parkinsonism in Brazil.

Parkinsonism & related disorders·2026

Genetic Testing for Neuromuscular Diseases.

Practical neurology (Fort Washington, Pa.)·2026

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

Related Concept Videos

The AE4 transporter mediates kidney acid-base sensing.

[Geminivirus replication: rolling circle mechanism in plants].

[Nanoviruses, small plant viruses: similarities and differences with geminiviruses].

Probabilistic tsunami forecasting for early warning.

Relationship between intervention dosage and success of resource connections in a social needs intervention.

Plasma levels of protein C pathway proteins and brain magnetic resonance imaging volumes in multiple sclerosis.

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A single-cell atlas of multiple myeloma defines malignant archetypes and proliferative states.

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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