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This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

Specific keratin gene mutations can cause monilethrix.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

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

LIPH mutations cause woolly hair in some Chinese people.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

A boy had a rare scalp condition with thickened skin and different-colored hair.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Hex gene plays a crucial role in starting feather development in chick embryos.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Hox genes control hair follicle stem cell regeneration in different body regions.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

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

The DWLSM provides detailed imaging of hair shafts and follicles with high accuracy.

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

A new gene mutation is linked to monilethrix in the studied family.

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

LX-38 is a safer drug option for treating prostate issues and hair loss without hormonal side effects.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

HS needs personalized treatment plans and more research.

A gene mutation causes monilethrix in a Chinese family.

Hair follicle cells can help keep embryonic stem cells undifferentiated.

Proper hedgehog signaling is crucial for maintaining healthy skin stem cells.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

Inhibiting HSP90 increases cell adaptability and survival under stress.