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Platelet-rich plasma may help restore immune balance in bald patches, but its effectiveness in treating hair loss is limited.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

The document concludes that stem cell inactivity is actively controlled and important for tissue repair and balance.

Akt2 protein is essential for normal cell division in early mouse embryos.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Tissue environment greatly affects the unique epigenetic makeup of regulatory T cells, which could impact autoimmune disease treatment.

New genes linked to male pattern baldness were found on chromosome 20p11.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

Hair removal with intense pulsed light can cause rare skin lesions that are hard to fully treat.

Alopecia areata in infants may be more common than previously thought.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

Regulatory γδ T cells help protect hair follicles from alopecia areata and promote hair regrowth.

Millets may help reduce chemotherapy side effects like nausea, fatigue, and hair loss.

γδTregs can protect hair follicles from alopecia areata and may help regrow hair.

KLF4 is important for keeping hair follicle stem cells inactive.

Stem cells from whiskers can be transplanted to stimulate hair growth.

New imaging technology can show up to 40 different markers in hair loss tissue, helping to understand hair disease better.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

Bacteria can help skin regenerate through a process called IL-1β signaling.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Activating β-catenin increases melanocytes and decreases Schwann cells.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Different genes are linked to various types of hair loss.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

Different immune responses cause hair loss in scalp diseases, with unique patterns in scalp psoriasis possibly protecting against hair loss.