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Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Keratin 15 expression in skin cells is regulated by two mechanisms involving PKC/AP-1 and FOXM1.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

The compound 4c showed strong potential as an anticancer agent.

Krox20 is important for cell differentiation in the brain and hair follicles.

CK15 is not a reliable marker for stem cells in damaged hair follicles from patients with CCCA.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

The prototype for analyzing skin aging works technically and clinically.

Different forms of FGF5 either promote or inhibit hair growth.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Deleting Crif1 in mouse skin disrupts skin balance and hair growth.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Impaired ABCA5 activity disrupts cholesterol balance in hair follicle cells, affecting hair growth.

CHI3L1 and CXCL5 proteins help promote hair growth.

K31 can identify clear secretory cells in human sweat glands.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Two new gene clusters important for hair formation were found on human chromosome 11.

NFIB and STAT5 work together to control specific genetic programs in cells.

Two new gene clusters important for hair formation were found on human chromosome 11.

A new mouse mutation causes skin and hair defects due to a gene change.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.