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Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

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.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Vitamin D receptor and hairless protein are essential for hair growth.

Vitamin D receptor is crucial for starting hair growth after birth.

GKLF/KLF4 and Sp1 control Keratin 19 gene activity, influencing cancer-related changes.

Researchers found two new genetic variants linked to Alzheimer's disease.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

A specific gene mutation causes congenital hair loss.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

MEX3A is crucial for maintaining intestinal stem cells in mice.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

Different keratins have unique expression patterns in mouse skin cells.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

TGM3 is important for skin and hair structure and may help diagnose cancer.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

Mutations in the KRT16 gene can cause skin and nail disorders.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

Hairless protein can block vitamin D activation in skin cells.

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

IL-18 signaling helps mature Tregs move into the thymus.

Targeting the TNFRSF1B gene may help treat hair loss.