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The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

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.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Trichohyalin is a versatile protein involved in hair and skin structure.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

A new mutation in the HR gene causes hair loss in a specific family.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

MOF controls skin development by regulating genes for mitochondria and cilia.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

Monilethrix is linked to a gene cluster on chromosome 12.

Researchers found a new mutation causing total hair loss from birth.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

A pathway helps maintain long telomeres in both stem and cancer cells.

The HR protein's role as a repressor is essential for controlling hair growth.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A peptide from hair follicle stem cells promotes hair growth by activating specific skin cells.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.