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Finasteride in male rats causes liver and metabolic issues in their offspring.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Hair evaluation is crucial for early diagnosis and management of ARCI, as hair loss often indicates severity.

DNA markers can predict physical traits for forensic use, but there are ethical and technical challenges.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

KAP8.1 gene variations affect cashmere weight in Inner Mongolian goats.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Certain genetic variants in keratins increase the risk of tooth decay.

Alopecia areata is influenced by genetics and immune system factors, and better understanding could improve treatments.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

Alopecia areata may be linked to atopic diseases like eczema, asthma, and allergies.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.

Key genes linked to wool quality in Spanish Merino sheep can improve fine wool production.

Two key genetic areas linked to male-pattern baldness were identified.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Combining genetic and physical data improves diagnosis and treatment for early-onset monogenic diabetes.

Alopecia is common in severe cases of autosomal recessive congenital ichthyosis.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

Key genes and pathways influence wool traits in Merino sheep.

Identified genes linked to male-pattern baldness may help develop new treatments.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

Certain genes influence the direction of hair whorls on the scalp.

Wool traits in sheep are controlled by many genes and environmental factors.