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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Keratin proteins in hair are complex and come from multiple gene families.

A KRT32 gene variant causes loose anagen hair syndrome.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Hair loss gene linked to prostate issues.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

A truncated protein linked to breast cancer may change cell adhesion.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Runx1 helps control the KAP5 gene in human hair follicles.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

The document introduced a new naming system for keratin-associated proteins to improve clarity and communication across species.

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

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

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Two new gene mutations cause a rare hair disorder.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

EDA2R gene linked to hair loss.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A specific gene change is linked to severe hair loss.