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Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

CXCR2 in skin cells promotes tumor growth.

IGN genes may regulate hair growth and could be targeted for hair-loss treatments.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

Planarians regenerate using conserved gene expression mechanisms, with runt-1 crucial for cell type specification.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A gene mutation causes monilethrix in a Chinese family.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Sheep cells were successfully modified to include a spider silk protein gene.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

FGFR2 signaling controls Merkel cell formation in different skin regions.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

ELL is crucial for gene transcription related to skin cell growth.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Targeting SOX proteins may improve cancer treatment by restoring immune function.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

Trichotillomania may have a genetic link to psychiatric disorders.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.