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Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

TGF-β2 helps activate hair follicle stem cells by counteracting BMP signals.

Eating too much or too little vitamin A can cause hair loss.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

People with alopecia have shorter hair follicles and more c-kit, a stem cell factor receptor, which could predict how the condition progresses.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

The study concluded that careful examination is key to differentiate between lipidized fibrous histiocytoma and juvenile xanthogranuloma.

RHUPUS should be considered in children with deforming arthritis.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

A Thai Bangkaew dog with diabetes and pancreatic issues improved with insulin, enzymes, and vitamins.

Some young Angus cattle had skin problems due to not enough vitamin A, which got better after they were given more vitamin A.

Skin symptoms are important for diagnosing and managing juvenile-onset systemic lupus erythematosus and usually get better with treatment.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Early diagnosis and treatment of systemic-onset juvenile idiopathic arthritis are crucial for improvement.

Some children with localized scleroderma are rarely resistant to methotrexate, and no common profile for resistance was found.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

PFOS exposure disrupts hormone levels and enzyme activities in juvenile frogs, affecting males and females differently.

Mycophenolate mofetil is effective for treating severe lupus nephritis in children.

A gene mutation in mice causes skin defects and early death.

FoxN1 overexpression in young mice harms immune cell and skin development.

Treatment during development affects hormone balance and sexual behavior in male rats.

Some treatments like methotrexate with prednisone might help juvenile morphea, but more research is needed to confirm.

Juvenile-onset lupus patients have more severe symptoms and need stronger treatment.