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Minoxidil decreases LH expression, while hydralazine has mixed effects on prolyl and lysyl hydroxylase activities.

Topical minoxidil may help improve hair growth in rare congenital hypotrichosis.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

The modified oriental prescriptions help hair growth and melanin production without irritating the skin.

Compounds from Monascus purpureus showed mild antifungal effects.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe symptoms and organ damage in mice.

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

Ets2 gene is crucial for placental development in mice.

Minoxidil does not work to inhibit lysyl hydroxylases in newborn mouse lungs.

Melatonin stops melanin production after tyrosinase action, with cyclic GMP mimicking this effect.

Alopecia mucinosa on the face can be linked to mycosis fungoides, a type of lymphoma.

Adding methionine to a low-protein diet helps Angora rabbits grow better fur.

Using fat-derived stem cells with the drug meglumine antimoniate can help control skin disease and reduce parasites in mice with leishmaniasis.

Biotin improved hair appearance in uncombable hair syndrome but didn't change hair structure.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

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

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

ACBP is crucial for healthy skin in mice.

Early diagnosis and treatment of myositis in SLE patients lead to positive outcomes.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Alopecia mucinosa is a challenging condition with unclear diagnosis and treatment.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Betamethasone activates and increases the growth of certain skin cells from hair follicles.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

A mutation in the Sgkl gene causes defective hair growth in mice.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.