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Activating mitophagy may help manage a key immune response involved in the hair loss condition alopecia areata.

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

LPA 4 helps control blood and lymph vessel development in zebrafish.

OsUEV1B protein is essential for controlling phosphate levels in rice.

PRAME is often present in Paget disease and could help in diagnosis, but more research is needed.

Targeting LPA could help treat skin disorders.

CAP1 helps Arabidopsis plants grow better under ammonium stress.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Phospholipase C-δ1 is crucial for normal hair development.

Enzymes that change arginine to citrulline are important for skin barrier and hair formation, and their malfunction can lead to skin conditions and hair disorders.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Loss of Rap1 protein speeds up heart aging in mice.

Two distinct pathways direct proteins to vacuoles in Arabidopsis, affecting root hair growth and protein targeting.

BAF200 is essential for proper heart and coronary artery formation.

p120-catenin helps control skin inflammation by regulating cadherin levels.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

PBX1 helps reduce aging and cell death in hair follicle stem cells by decreasing DNA damage, not by improving DNA repair.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.