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Dermatologists are crucial for managing skin side effects in metastatic melanoma patients using vemurafenib and ipilimumab.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Two new gene mutations cause a rare hair disorder.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

Platelet-rich fibrin may help reduce nonmelanoma skin cancer cell growth.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Certain genes are more active during wound healing in axolotl and Acomys, which could help develop materials that improve human wound healing and regeneration.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

BRG1 is essential for skin cells to move and heal wounds properly.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

PTCH gene mutations contribute to basal cell carcinoma development.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Brepocitinib effectively reduces inflammation and improves symptoms in cicatricial alopecia with good safety.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

BMP2 and BMP7 have opposite roles in feather formation.

The new chemotherapy combination of WP 631 and Epothilone B shows enhanced effectiveness against ovarian cancer but requires more research on its safety.

p120-catenin helps control skin inflammation by regulating cadherin levels.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

Normal human melanocytes can avoid cell death through multiple pathways.