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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

Early recognition and a multidisciplinary approach are crucial for effectively managing complex autoimmune conditions like SLE with CAPS and AHA.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

People with autism are more likely to develop alopecia areata than those without autism.

A 14-year-old girl with severe hair loss regrew her hair using upadacitinib.

Scientists made stem cells that can grow hair by adding three specific factors to them.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

BroadAMP-GPT effectively creates antimicrobial peptides to fight drug-resistant bacteria.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

A new treatment using unactivated platelet leukocyte autoplasma cured 80% of non-scarring alopecia patients.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

JAK1 inhibitor may effectively treat alopecia areata when TNF-α inhibitors and corticosteroids fail.

Desmocollin 1 helps maintain skin structure during fetal development.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

Generative AI tools can accurately score alopecia areata, reducing subjectivity in evaluations.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The ASIP gene is crucial for determining cattle coat color.

Alopecia areata causes patchy hair loss and involves immune system disruptions.

Two distinct pathways direct proteins to vacuoles in Arabidopsis, affecting root hair growth and protein targeting.

APKH in young males may signal early hair loss and needs early attention.

ATR is crucial for DNA repair and cell survival after UV exposure.

ADSCs help protect skin from UV damage and aging.

PDE inhibitors, especially PDE4 inhibitors like apremilast, are effective for certain inflammatory skin conditions but have side effects and can be costly.

Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

FFA can be mistaken for rosacea, requiring specific treatment for accurate diagnosis and management.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Targeting the protein Caveolin-1 might help treat a type of scarring hair loss called Frontal Fibrosing Alopecia.