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Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Aryl hydrocarbon receptor overexpression found in miniaturized hair follicles in female hair loss.

CUX1 boosts sheep hair cell growth and affects curl patterns.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

ERULUS is crucial for root hair growth by controlling calcium levels.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Gene expression affects fur development in rex rabbits.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

Modified stem cells from umbilical cord blood can make hair grow faster.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The commentary explains that a balance of HR protein and putrescine is important for normal hair growth.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

Inhibiting ODC can prevent UV-induced skin cancer.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

uPA helps hair follicle cells grow.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

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

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Urokinase, a type of protein, helps skin cells multiply faster, especially in newborn mice.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Exosomes from stem cells can reduce UV-induced skin damage by lowering inflammation and oxidative stress.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.