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The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

The p53 protein helps control hair follicle shrinking by promoting cell death in mice.

A new mouse mutation causes skin and hair defects due to a gene change.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

Akt2 and SGK3 are both important for normal hair growth and development.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

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

The research identified specific genes that are active in the cells crucial for hair growth.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Mutations in hKAP1 genes may cause hereditary hair disorders.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Targeting the p63 gene could help treat skin diseases.

A new gene, JMJD1C, may affect testosterone levels in men.

Lack of cystatin M/E causes thin hair and dry skin.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Sp6 promotes tooth development by reducing follistatin levels.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

cDermo-1 causes dense skin, feathers, and scales in chickens.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Mutations in the SNRPE gene cause hereditary hair loss.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Controlling Tslp can improve health in AEC syndrome patients.

A new genetic mutation was found causing hair and eye issues in a boy.