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Colorectal cancer cells can adapt without losing their traits or drug sensitivity.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Hoxc13 and hair keratin are needed for forming rough skin on frog mating pads.

Keratin proteins are crucial for hair growth and structure.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Keratins K6 and K16 are expressed more freely in regenerating mouse skin than K1 and K10.

Two new gene clusters important for hair formation were found on human chromosome 11.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

KLHL24-mutant stem cells help understand skin and heart disease.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

The study suggests that the arrector pili muscle is important for hair health and its damage might contribute to hair loss.

Glycyrrhizinic acid spray showed limited effectiveness in treating anogenital warts in HIV patients with low CD4 levels.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Mice with the naked gene have missing or abnormal hair cells.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Certain gene variations are linked to the thickness of cashmere goat hair.

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

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The Naked gene in mice causes abnormal sebaceous glands and disrupts hair follicle organization.