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FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

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

Two new gene clusters important for hair formation were found on human chromosome 11.

K25, K27, and K28 are found in all inner root sheath layers of hair, while K26 is only in the cuticle.

New compounds show promise for treating benign prostate hyperplasia with fewer side effects.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

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

Higher CRBP1 levels are linked to more severe alopecia areata.

Mutations in specific llama genes may affect fiber quality for textiles.

SRD5A2 methylation in blood can predict how well someone will respond to finasteride treatment.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

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

p2y5, now called LPA6, is a receptor important for human hair growth.

A missing mK6irs1 gene causes hair loss in mice.

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

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.