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Treating psoriasis on the scalp, nails, and skin folds is challenging, often requiring systemic treatments for severe cases, with some success in topical and biologic treatments.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

One minoxidil-sensitive potassium channel exists in human hair follicles.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

The sebaceous gland has more roles than just producing sebum and contributing to acne, and new research could lead to better skin disease treatments.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

Treatments for permanent hair loss from scarring aim to stop further loss, not regrow hair, and vary by condition, with partial success common.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

The Wnt/β-catenin pathway helps tissue regeneration but can also cause fibrosis, and drugs that inhibit this pathway may aid in healing skin and heart tissues.

Improving skin barrier and using antifungal treatments can help manage dandruff.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

Wnt signaling helps control how brain stem cells divide and is important for brain repair after injury.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The Wnt/β-catenin pathway is important for tissue development and has potential in regenerative medicine, but requires more research for therapeutic use.

Using nanostructured lipid carriers to deliver spironolactone could improve treatment for hair loss.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Activating the Wnt/β-catenin pathway could lead to new hair loss treatments.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Mutant mice help researchers understand hair growth and related genetic factors.

NF-κB is crucial for zebrafish heart repair, affecting heart cell growth and repair processes.

Liposomes better deliver minoxidil for hair loss treatment than niosomes.

Treatments for melanin disorders exist, but more effective options needed.

Skin development in mammals is controlled by key proteins and signals from underlying cells, involving stem cells for maintenance and repair.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

Caffeine penetrates human skin in lab tests similarly to real-life conditions, but actual skin use is still essential for accurate results.