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Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

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

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

Genes controlling hair growth and immune response are disrupted in male pattern baldness.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Androgens increase muscle mass by promoting myoblast growth through ornithine decarboxylase.

Monilethrix is linked to a gene cluster on chromosome 12.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

CD25+ CD4+ Tregs and certain plasma proteins are linked to hair loss.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

Adenine helps delay aging in human hair follicle cells.

OR2AT4 helps reduce aging and cell damage in human skin cells.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Mutations in the androgen receptor gene cause androgen insensitivity, leading to female traits in genetically male individuals.

The research found genes that may protect certain scalp cells from hair loss.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

Genetic discoveries are leading to new treatments for alopecia areata.