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Patients in Australia underwent costly, unproven stem cell treatments due to weak regulations and aggressive marketing.

Alopecia areata may be treated by using EGCG to balance immune cells and reduce inflammation.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

ILC1-like cells can cause alopecia areata by attacking hair follicles.

Dermatologists vary widely in testing practices for alopecia areata, often exceeding guideline recommendations.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A new patch can deliver stable antibodies over time for potential HIV treatment.

New mutations in the hairless gene may cause hair loss and affect bone development.

IFN-γ production by CD4 T cells is crucial for causing alopecia areata.

CD2 might be a new treatment target for patchy alopecia areata.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

BTNL2 helps protect hair follicles from immune attacks.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

AGA patients have higher heart disease risk.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Farudodstat may effectively treat alopecia areata without harming hair follicles.

Certain gene variations may increase the risk of hair loss in Egyptians.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

The document concludes that reactivation of herpesviruses, especially HHV-6, is linked to severe symptoms and complications in drug-induced hypersensitivity syndrome.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.