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Applying a DNA vaccine to skin with active hair growth boosts immune response and protection against anthrax in mice.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

A 3-year-old boy had a rare hairball condition usually seen in teenage girls.

Human hair follicles can be used to create stem cells that might help clone hair for treating hair loss or helping burn patients.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Alopecia areata greatly affects people's life quality, mental health, and work life.

Transgender youth have more sleep disorders, but gender-affirming therapy may help reduce them.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Trichotillomania treatment is most successful with a mix of behavioral therapy, medication, and social support.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

High DHA levels delay wound healing and worsen skin repair quality.

Some antiseizure medications can cause cosmetic problems like hair loss, excessive hair growth, acne, and gum overgrowth.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Exosomes from dermal papilla cells help hair follicle stem cells grow and survive.

Adipose-derived stem cells help heal burns but need more research.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

The study found that androgen receptors in skin cells mainly affect the focal adhesion pathway and control the caveolin-1 gene, with implications for new treatments for related diseases.

HA-stimulated stem cell vesicles improved hair growth in male mice with androgenetic alopecia.

Human hair keratin might be good for filtering out harmful substances from water.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Targeting lipid metabolism can help treat advanced, resistant cancers.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.

Diphenyl cresyl phosphate has low toxicity but can harm the liver, kidneys, adrenal glands, and testicles at high doses.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

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