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The protein DDX6 helps keep skin cells renewing properly by controlling the production of certain other proteins and breaking down those that cause cells to mature too quickly.

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BI 2536 had limited effectiveness against several advanced cancers and caused significant side effects.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

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

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

The new keratin film without KAPs stains better and could help study keratin functions.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Interleukin 6 may help protect skin without causing inflammation.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

Trametinib can effectively treat severe kaposiform lymphangiomatosis when other treatments fail.

BFNB could be a promising treatment for hair growth.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

Keratin-associated proteins are crucial for hair strength and structure.

Inward rectifier potassium channels are important in many body functions and diseases, and could be potential drug targets.

Different combinations of human hair keratins affect how hair fibers form.

KGF and its receptor are found in enlarged prostate tissue and KGF strongly increases cell growth.

B6J mice live longer before 24 months, but B6N mice live longer after; both strains show weight gain, increased food and water intake, and health issues as they age.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

The N-K GM Series offers a new method to reduce aflatoxin poisoning and cancer, improving health and saving costs in affected regions.

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

Krox20 (Egr2) is important for the function of epithelial stem cells.

KFSD causes scarring hair loss and skin roughness, mainly in males.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.