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A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The treatments stopped hair regrowth in mice.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A mutation in the human hairless gene causes alopecia universalis.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

New genetic mutations linked to rare skin disorders were found in three newborns.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Different γδ T cell types have unique roles in causing alopecia areata.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

There is a significant need for better-validated quality of life tools in dermatology.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

Hairless gene not strongly linked to baldness.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Plasmacytoid dendritic cells, which overproduce IFN-α, may play a crucial role in starting alopecia areata, an autoimmune disease causing hair loss.

The Dermatology Life Quality Index is reliable and consistent but needs more diverse participant studies.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.