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Hair loss in male pattern baldness is linked to changes in specific genes and proteins that affect hair growth and scalp health.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

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

A new method helps find proteins in hair to identify fetal growth issues.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

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

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

Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

HOXC13 is essential for hair and nail development by regulating Foxn1.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

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

Sonic hedgehog signaling is crucial for hair growth and maintaining hair follicle identity.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

TNFα, IFNγ, and Substance P significantly affect prolactin levels in human skin, suggesting new treatments for skin and hair conditions.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

A new method improves protein extraction from hair, helping identify potential biomarkers for fetal growth issues.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Human dermal fibroblast proteins help restore nerves during healing.

Phospholipids help plant proteins move by regulating receptor interactions.

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

Protein microarrays are highly sensitive tools useful for disease diagnosis and studying proteins.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.