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Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Glycoproteins are present in the cell membranes of various keratin fibers.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Histone H4, released by cells exposed to colchicine, can cause hair loss by inhibiting cell growth and enzyme activity.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

Automatically measuring ferritin can help identify iron deficiency in women with hair loss.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Human hair protein extracts can protect skin cells from oxidative stress.

Hair is mostly made of three protein types: helical, high-sulfur, and high-tyrosine.

Avoiding aspirin may prevent hair loss.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Human liver enzyme DHEA ST helps process minoxidil.

Hair fibers may have a unique, non-protein sheath not previously identified.

Hirsutism is excessive male-pattern hair growth in women, often treated cosmetically or with hormone therapy if contraception is also desired.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

The method ensures Hibiscus rosa-sinensis flower extract is safe and effective for medicinal use.

Iron deficiency can cause hair loss and often signals underlying health issues.

Females have higher estrogen receptor levels in hair than males, and these levels decrease in white hair compared to black hair.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

Homeopathy may help treat hair loss and improve quality of life.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

High-dose iron therapy improves anemia without affecting IBD treatment.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

High-dose intravenous iron therapy doesn't interfere with treatment improvements in IBD patients with iron deficiency anemia.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.