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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.

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

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

A new mutation in the HR gene causes hair loss in a specific family.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

pdHGF speeds up wound healing and hair growth.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Higher antigliadin antibodies are linked to more severe alopecia areata, suggesting screening for celiac disease in these patients.

A patient with HAIR-AN syndrome, PCOS, and Hashimoto's thyroiditis improved with early diagnosis and treatment to prevent serious health problems.

A man with severe hair loss regrew hair after hormone treatment.

AGA linked to inflammation, stress, fibrosis, and disturbed hair follicle stem cells.

Men with early baldness have similar heart risk factors as others, but certain proteins are linked to higher heart disease risk.

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

Androgenetic alopecia, or hair loss, is caused by genetic factors and hormones, with different mechanisms in men and women, and can be linked to insulin resistance and polycystic ovary syndrome.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

New treatments for common hair loss are needed.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

A new gene mutation causes a rare type of hair loss.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Gender-affirming hormone therapy improves mental health and gender incongruence but requires careful management of cardiovascular and cancer risks.

The solution increased hair density safely and effectively for hair loss.