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ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

Bendamustine combined with tucidinostat may effectively treat adult T-cell leukemia.

Polydopamine is promising for personalized medicine and biomedical technology due to its strong adhesion and biocompatibility.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

The hydrogel dressing RD@PVA helps heal diabetic wounds by reducing stress and improving blood vessel growth.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Low-dose oral and topical minoxidil are recommended for managing hair loss in transplant patients, with specific dosing and timing guidelines.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

Minoxidil helps restore thymus size in 22q11.2 deletion syndrome.

ADM scaffolds help skin heal by promoting a healing-type immune response.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Longer immunotherapy treatment may improve outcomes for Merkel cell carcinoma patients.

Disruptions in mammary stem cell division can lead to cancer, but targeting these processes might help treat breast cancer.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Corticosteroids, especially prednisone, improve short-term muscle strength in Duchenne muscular dystrophy but have manageable side effects.

wAMD patients have higher oxidative stress, suggesting antioxidant treatment may help.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Adding dutasteride to therapy may improve treatment for advanced salivary duct cancer.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The combination of Lucilia sericata larva secretions and Achillea sintenisii extract significantly improves wound healing in diabetic rats.