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A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

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

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

The MLPH gene is not linked to seasonal hair loss in Rhodesian Ridgeback dogs.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

The antibody created from BCC tissues reacts similarly to both BCC and hair follicles, suggesting BCC may come from hair follicle cells.

Farudodstat may help treat alopecia areata by protecting hair follicles.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

Certain genetic markers may increase or decrease prostate cancer risk.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

Researchers found a gene mutation responsible for a rare hair loss condition.

Tph cells are linked to the severity of systemic lupus erythematosus.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Alopecia areata shows a unique type 1 interferon signature, suggesting potential treatment by targeting this pathway.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

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

CT60 polymorphism might increase the risk of Alopecia Areata.

Human hair contains a substance that shows blood group A activity.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.