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A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

MicroRNAs are crucial in controlling cell signaling, affecting cancer and tissue regeneration.

Mrp3 may aid in wound healing and hair growth.

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

MicroRNAs play a key role in wool growth in Tibetan sheep.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

New LSS gene variants help understand congenital hypotrichosis 14 better.

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

SLCO genes may predict prostate cancer mortality risk, and lifestyle changes improve health in advanced prostate cancer.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

NGAL indicates abnormal skin cell differentiation.

A specific gene change is linked to severe hair loss.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Goats' hair and color traits are linked to specific RNA expressions, useful for breeding and textiles.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Chemotherapy-induced hair loss is partly due to decreased laminin-511 and increased laminin-332.

Removing certain immune cells in mice causes their hair to enter the growth phase earlier than usual.

Suppressing eIF4E can prevent hair loss from chemotherapy.

Aromatase gene variation may increase female hair loss risk.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

Reducing miR-30a-5p helps hair follicle stem cells grow and survive.