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Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

A mutant FERONIA gene affects root hair growth at high temperatures.

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

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Targeting THY1 can improve skin repair and healing.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

L-threonate may help prevent balding by blocking a key hair loss factor.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Keeping human skin stem cells is easier with low temperatures and mTOR inhibition.

L-threonate may help prevent balding by blocking a key protein.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

New mutations in the hairless gene may cause hair loss and affect bone development.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

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

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

ATR04-484 ointment shows promise for treating skin issues from cancer therapies.