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Extracellular vesicles could offer precise treatments for psychiatric conditions by targeting brain networks.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Fahr syndrome causes brain calcification and is managed by treating symptoms and underlying issues.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

Gut bacteria overgrowth may cause some Post-Finasteride Syndrome symptoms.

These gene variations are not linked to alopecia areata in Egyptians.

Syphilitic alopecia is a rare hair loss condition in secondary syphilis that looks similar to another condition but can be diagnosed with specific tests and responds to antibiotics.

Finasteride may help treat Neutrophil Actin Dysfunction by reducing LSP1 gene activity.

Autophagy is important for determining the protein makeup of hair.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Hair glycation can indicate long-term blood sugar levels and diabetic nerve issues.

Hair analysis can help identify specific minerals and amino acids linked to various diseases.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Transglutaminase-3 is often reduced in esophageal cancer.

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

Managing myasthenia gravis is crucial and does not worsen primary Sjögren's syndrome.

A specific gene mutation causes congenital hair loss.

A man with hair loss and a scalp lump was diagnosed with a diffuse neurofibroma but chose not to have surgery.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.