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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Krtap11-1 is important for hair strength and structure.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Lack of KSR1 stops certain skin tumors in mice.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Patched1 helps prevent tumors by controlling cell growth.

HPV type 56 can hide in hair follicles even without visible warts.

Sex and race affect immune responses and treatment outcomes in Hidradenitis suppurativa.

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

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

BMP receptor IA is essential for proper hair cell differentiation in mice.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.