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Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Whn is essential for hair growth, and its malfunction causes hair loss.

Certain genes are linked to the risk of developing Alopecia Areata.

The N gene affects the protein makeup of mouse hair.

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

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

HuR is essential for Treg function and preventing autoimmunity.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

DNA methylation controls lncRNA2919, which negatively affects hair growth.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

Different keratins have unique expression patterns in mouse skin cells.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Protein ubiquitylation is crucial for controlling stem cell functions and could be targeted for cancer treatment.

Keratin 17 is crucial for cell growth in wound healing by aiding protein synthesis.

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

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Dermal EZH2 controls skin cell growth and differentiation in mice.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

Altering SSAT affects fat metabolism and body fat in mice.