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A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

High TSPEAR levels in colorectal cancer predict worse outcomes.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

TRASER effectively targets blood vessels and hair follicles for potential use in vascular and hair removal treatments.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

STIM1 is essential for sweat secretion.

Krtap11-1 is important for hair strength and structure.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Sex hormones may be linked to inflammation in Hidradenitis Suppurativa.

The Itpr3 gene causes a specific hair pattern in mice.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

Androgens regulate Sertoli cells and affect fertility through specific receptors and coregulators.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

In Singapore, most skin reactions to drugs were in females and Chinese, often caused by painkillers, antibiotics, and some other drugs, with serious cases linked to genetics.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Hormones and sex affect potassium channel gene expression in electric fish, influencing their communication signals.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

TRPV1 is involved in pain, various body functions, and diseases, but targeting it for treatment is challenging.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

A genetic variant linked to hair thinning in Japanese women was found.

DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

Blocking neurosteroid production can lead to more seizures and faster epilepsy onset in rats.

Spironolactone reduces the number of androgen receptor sites in rat skin by blocking them with its metabolite.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.