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The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

High TSPEAR levels in colorectal cancer predict worse outcomes.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

AGD1's PH domain is essential for its role in root hair growth and polarity.

PAR-1 may play a role in hair growth regulation in human hair follicles.

Hsc70 protein may influence hair growth by responding to androgens.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

20(S)-Protopanaxadiol-aglycone may help prevent and treat prostate cancer by reducing androgen receptor activity.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A peptide from hair follicle stem cells promotes hair growth by activating specific skin cells.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Mutations in hKAP1 genes may cause hereditary hair disorders.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

H3K4me3 helps control RSPO3 to influence hair growth and development.