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A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Low-penetration genes might help personalize colorectal cancer prevention.

AMPK activation may reduce melanoma risk in red-haired individuals.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

The rs1128977 gene variant may affect cholesterol and body measurements.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

Notch/RBP-J signaling is crucial for proper placement and timing of melanocyte development in hair follicles.

A mutation in mice causes hair loss and immune problems.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A new gene variant causes curly coats in some dog breeds.

The HCR gene contributes to psoriasis risk.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Mcl-1 can activate Wnt signaling in skin cells, promoting growth and possibly cancer.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

NFIB and STAT5 work together to control specific genetic programs in cells.

A new mouse mutation causes skin and hair defects due to a gene change.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

Trps1 is essential for proper hair follicle development.

A girl with Evans' syndrome had her low platelet count successfully treated with zanubrutinib.