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A specific RNA can help hair growth in baldness by boosting stem cell activity.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

Hsc70 protein may influence hair growth by responding to androgens.

ILC1-like cells can cause alopecia areata by themselves.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

miR-148a and miR-10a affect hair growth in Hu sheep.

Ber‐EP4 marks cells related to the secondary hair germ in hair follicles.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

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

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

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

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

PPAR-γ may be a key target for treating alopecia areata and other skin conditions.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

The hairless protein is important for skin, hair, and may influence cancer development.

The UHS promoter is specific to mouse hair follicles.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

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

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

STAT5 activation is crucial for starting the hair growth phase.