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Oral and topical tranexamic acid effectively and safely improve melasma.

Mannosylerythritol lipids are good for skin and hair care products.

Mammary stem cells drive mammary gland growth by branching and cell mixing.

Ethinylestradiol/Chlormadinone Acetate is a safe and effective birth control pill that also helps regulate menstrual cycles, reduces period pain, and treats certain skin and hair conditions.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

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Ethinylestradiol/chlormadinone acetate may be an effective and well-tolerated treatment for skin conditions caused by excess androgens.

Matriptase is crucial for skin, hair, and immune cell health, and its imbalance can lead to cancer.

Sulfur mustard damages hair follicles and sebaceous glands in mice.

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

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Benign follicular mucinosis involves immune cells attacking hair follicles.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

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

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Neuromyotonia and morphoea can occur together in the same body areas.

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A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

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

Skin cancer often starts from Lgr5+ progenitor cells.

PRAME is often present in Paget disease and could help in diagnosis, but more research is needed.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Specific keratin gene mutations can cause monilethrix.

Mesenchymal MEIS2 is essential for whisker development without needing sensory nerves.