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The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Skin grafts from related donors significantly healed chronic wounds in patients with a severe skin condition over a year.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

A gene mutation causes woolly hair in a Syrian patient.

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.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

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

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

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

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

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

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.