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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

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

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Suppressing ODC activity reduces tumor growth in hair follicles.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

ILC1-like cells can cause alopecia areata by themselves.

Keratoacanthomas and squamous cell carcinomas have similar keratin patterns, making them hard to tell apart.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

Activating β-catenin in certain skin cells speeds up hair growth in mice.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

ELL is crucial for gene transcription related to skin cell growth.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

CD4+ skin cells may be precursors to basal cell carcinoma.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

EGFR deficiency in skin causes hair follicle issues and inflammation.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.