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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

AKR1C enzymes in scalp glands decrease with age, possibly affecting hair loss.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

KAP8.2 gene variations affect cashmere quality in goats.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Caffeic acid helps protect rats from the harmful effects of acrylamide.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

p2y5, now called LPA6, is a receptor important for human hair growth.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

The ACE1 gene variant doesn't affect long-COVID symptoms.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Scientists made new substances that can block an enzyme linked to prostate issues and hair loss, with potential for creating a new treatment.

Hair-straightening products with glyoxylic acid can cause kidney damage.

A gene mutation in mice causes skin defects and early death.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Rac1 is essential for proper hair structure and color.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.