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ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

L-threonate may help prevent balding by blocking a key hair loss factor.

Both HLA-B and MICA are independently linked to alopecia areata.

Inflammasome proteins can indicate the severity and treatment response of various diseases and injuries.

MEX3A is crucial for maintaining intestinal stem cells in mice.

Autophagy is important for determining the protein makeup of hair.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

RIPK1 inhibitors may help prevent alopecia areata by reducing immune cell activity.

Skin cancer often starts from Lgr5+ progenitor cells.

Caspases affect many cell functions and could help treat various diseases.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

MitoQ may help treat hair loss by boosting hair growth pathways.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Miz1 is essential for proper hair structure and growth.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A genetic variant in the KRT25 gene causes tightly curled hair.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.