Evidence for extensive locus heterogeneity in Naxos disease

Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?

Experimental dermatology·2026

Cell-to-cell variability and gain of methylation at polycomb CpG islands as a hallmark of aging.

Nature communications·2026

Multicytokine-based transcriptome-wide association study for 7 inflammatory skin disorders identifies candidate causal genes in keratinocytes.

The Journal of allergy and clinical immunology·2026

Baricitinib Augments Lonafarnib Therapy to Preserve Colonic Homeostasis and Microbial Balance in a Mouse Model of Progeria.

Aging cell·2025

Deregulated miR-145 and miR-27b in Hutchinson-Gilford progeria syndrome: implications for adipogenesis.

Aging·2025

Impact of miR-181a on SIRT1 Expression and Senescence in Hutchinson-Gilford Progeria Syndrome.

Diseases (Basel, Switzerland)·2025

Chimeric antigen receptor T-cell therapy in dermatologic autoimmunity: Mechanisms, applications, and future directions.

The Journal of investigative dermatology·2026

Part I. Quantitative provocation and assessment of cutaneous pain in experimental systems: Methods, techniques, and applications.

The Journal of investigative dermatology·2026

Part II. Measuring skin pain in humans: Quantitative, psychophysical, and patient-reported tools for dermatology.

The Journal of investigative dermatology·2026

Circadian skin pH gates IL-33 and remote food sensitization.

The Journal of investigative dermatology·2026

Inhibition of Salt-Inducible Kinases 2 and 3 reduces inflammatory signature in Psoriasis.

The Journal of investigative dermatology·2026

Regulatory T cells: From Foxp3 to tolerance-inducing therapies.

The Journal of investigative dermatology·2026

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Bioinformatics (Oxford, England)·2026

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Drug metabolism and personalized therapy·2026

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

Current medicinal chemistry·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

Related Experiment Videos

Evidence for extensive locus heterogeneity in Naxos disease

Related Concept Videos

Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?

Cell-to-cell variability and gain of methylation at polycomb CpG islands as a hallmark of aging.

Multicytokine-based transcriptome-wide association study for 7 inflammatory skin disorders identifies candidate causal genes in keratinocytes.

Baricitinib Augments Lonafarnib Therapy to Preserve Colonic Homeostasis and Microbial Balance in a Mouse Model of Progeria.

Deregulated miR-145 and miR-27b in Hutchinson-Gilford progeria syndrome: implications for adipogenesis.

Impact of miR-181a on SIRT1 Expression and Senescence in Hutchinson-Gilford Progeria Syndrome.

Chimeric antigen receptor T-cell therapy in dermatologic autoimmunity: Mechanisms, applications, and future directions.

Part I. Quantitative provocation and assessment of cutaneous pain in experimental systems: Methods, techniques, and applications.

Part II. Measuring skin pain in humans: Quantitative, psychophysical, and patient-reported tools for dermatology.

Circadian skin pH gates IL-33 and remote food sensitization.

Inhibition of Salt-Inducible Kinases 2 and 3 reduces inflammatory signature in Psoriasis.

Regulatory T cells: From Foxp3 to tolerance-inducing therapies.

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

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Related Experiment Videos

Evidence for extensive locus heterogeneity in Naxos disease

Related Concept Videos

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