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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.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

Different types of cells in the eye express specific keratins at various stages of development.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

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

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Keratinocyte growth factor significantly alters skin and tissue development.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Keratin 15 affects cell behavior and characteristics in skin cells.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

Septin4 helps kill colon cancer cells by working with the protein BAX.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

BIK1 gene helps plants resist some pathogens but makes them more vulnerable to others.

Brepocitinib effectively reduces inflammation and improves symptoms in cicatricial alopecia with good safety.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

OR2AT4 helps reduce aging and cell damage in human skin cells.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

RXR agonists may promote hair growth in humans.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

CRH can cause hair loss by promoting cell death in hair growth cells.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Cepharanthine and berbamine may affect SK channels, influencing their therapeutic effects.