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RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

Hydroxychloroquine may cause false results in tuberculosis tests for patients with autoimmune skin diseases.

IL-15 helps protect hair follicles from immune attacks and encourages hair growth.

Alopecia areata may be caused by antibodies targeting specific hair follicle proteins, hindering hair growth.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

Alopecia areata can be an early sign of Hodgkin’s lymphoma and may improve with lymphoma treatment.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

The research developed methods to test drugs that could protect and restore hair follicle protection in a hair loss condition.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

hHbl gene is active in hair shaft cells and some pilomatricomas.

The laser therapy device effectively increased hair growth in people with androgenetic alopecia.

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

A rare combination of hair loss and excessive fine hair growth was found in celiac disease patients.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Hair loss treatment caused more hair loss in a man.

Skin diseases are common in HIV patients and could help detect HIV early in Ethiopia.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Children with alopecia areata should only get thyroid screening if they have Down syndrome, a family history of thyroid disease, atopy, or signs of thyroid problems.

A 5 cm hair sample can reveal blood type and keratin type for forensic use.

A mutation in the IL2RA gene increases the risk of alopecia areata.

People with alopecia areata may have a higher risk of thyroid diseases.

The assay effectively identifies compounds that affect immune cell activation.

High levels of HSP70 and IL-15 are linked to more severe alopecia areata.

Sweet syndrome can be the only sign of hairy cell leukemia relapse.