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A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

AIMP1 can boost hair growth by increasing stem cell activity.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

HPV8 E6 gene causes growth of certain skin stem cells.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Fatty acid transport protein 4 is essential for skin and hair development.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

Cathepsin L deficiency causes hair and skin issues in mice.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

N1-acetylspermidine promotes hair follicle stem cell self-renewal.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

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

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

RXRα is crucial for proper immune response and links diet to immune function.

WNT10A gene mutations cause short anagen hair syndrome.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Consider NF1 in newborns with rare congenital anomalies.

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

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.