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A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

FMH foods may help manage post-acute COVID-19 symptoms safely and easily.

The new assay can help develop products for hair re-growth.

The HCR gene contributes to psoriasis risk.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

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

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

CTCF protein is essential for skin and hair follicle development in mice.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

CDP is crucial for lung and hair follicle cell development.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

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

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

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