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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

GhPLDα1 helps thicken cotton fiber walls by boosting cellulose production.

Microneedles improve drug delivery, patient compliance, and have potential in cancer treatment and skin care.

A woman with Castleman's disease died from respiratory failure due to bronchiolitis obliterans.

Recognizing race-specific skin traits is crucial in pediatric dermatology.

Reflectance confocal microscopy is useful for diagnosing and monitoring skin diseases, but it has limitations and requires expertise for correct use.

Gefitinib can cause hair and eyebrow darkening.

Early screening and HPV vaccination reduce cervical cancer risk.

Nerve cells and other cell types work together to start horn growth in dairy goats.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Midscalp hair density and terminal hair percentage are good indicators of female pattern hair loss severity.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Sirolimus can reduce tumor cell size in TSC-related skin tumors, but continuous treatment is needed to maintain benefits.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Telogen effluvium is a common hair loss condition requiring careful diagnosis and treatment.

Dermatologists should address discrimination and consider ethnic and gender differences in treatments.

Patients treated in Respiratory Intensive Care Units for COVID-19 are more likely to get mood disorders than those in other care settings.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

A rare case shows a possible link between Neurofibromatosis type 1 and Becker nevus due to genetic mutations.

Hair patterns in mice are controlled by both a global system dependent on Fz6 and a local self-organizing system.

Dermal white adipose tissue helps regulate hair growth, protect skin, and aid wound healing.

Male and female mice handle stress differently.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Corneal cells can potentially revert to stem cells, aiding in repair and regeneration.

Adult mouse skin contains stem cells that can create new hair, skin, and oil glands.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

Stress can cause hair to turn gray by depleting stem cells.