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Certain plasma proteins and genes are linked to obstructive sleep apnea, suggesting potential new treatments.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Different androgen concentrations affect wool-related gene expression differently in Hetian and Karakul sheep breeds.

A protein called sFRP4 from skin cells stops the development of pigment-producing cells in hair.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Targeting NETs may help reduce fibrosis in Crohn's disease.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

Vitamin D receptor gene changes don't affect alopecia areata risk.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Robertsonian translocation can cause recurrent miscarriages.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

Goat skin has more keratin genes, while the mammary gland has more immunity-related genes.

Activated ras can protect kidney cells from a certain substance that causes cell death.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

UC.145 may be a new biomarker for predicting gastric cancer.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Certain genes in European Merino sheep help them adapt to different climates.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Researchers developed a new way to measure gene activity in single hair follicles and found that a specific gene's activity changes with different amounts and times of treatment.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.