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ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

rhKGF2 significantly promotes hair growth and follicle development.

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

A gene mutation in mice causes severe skin disorder similar to a human condition.

Blocking the KATP channel may help treat migraines.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Keratinocyte Growth Factor-Hair Serum may help prevent hair loss during chemotherapy, but more research is needed.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

The EG7 foam dressing improved wound healing and reduced inflammation better than other treatments.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Keratin heterodimers are preferred for their specific and structural advantages.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

CIP/KIP proteins help stop cell division and support hair growth.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A 9-year-old girl with a healthy immune system was successfully treated for a severe fungal scalp infection caused by Microsporum audouinii.

The fuzzy gene is crucial for controlling hair growth cycles.