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New biomarkers and potential treatments for skin diseases were identified.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Raltitrexed conjugates are less potent than the free drug but more effective at high concentrations.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.

Targeting SOX proteins may improve cancer treatment by restoring immune function.

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

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Low-dose naltrexone helps improve symptoms and stabilize frontal fibrosing alopecia and lichen planopilaris.

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

IMG-007 helps regrow hair and reduce scalp inflammation in severe alopecia areata.

Low-dose naltrexone might be a cheap and effective additional treatment for hair loss with scalp discomfort due to its anti-inflammatory effects and few side effects.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Ocu-miR-205 helps control hair growth in Rex rabbits by affecting cell processes and signaling pathways.

miR-22 helps skin cancer grow and spread by activating specific cell signals.

ocu-miR-205 affects hair density in Rex rabbits by altering hair follicle growth and signaling pathways.

A specific gene mutation causes congenital hair loss.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

SQSTM1 is linked to increased risk of alopecia areata.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.