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Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Phospholipase C-δ1 is crucial for normal hair development.

Trichothiodystrophy causes unusual hair and developmental issues.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Trichohyalin is a protein in hair follicles that helps form hair filaments.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Bcl-2 helps hair regeneration but can also increase cancer risk.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Controlling Tslp can improve health in AEC syndrome patients.

HOTTIP and miR-10b contribute to glioma therapy resistance by affecting cell behavior, suggesting they could be targets for treatment.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

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

TAT-GILZ peptide promotes hair growth by boosting stem cell activity.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

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