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A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Melatonin affects when and how certain genes work during the different stages of goat hair growth.

EGFR deficiency in skin causes hair follicle issues and inflammation.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

MTS24 marks a new type of skin cell that helps hair growth and repair.

Keratin hydrogels can be customized for better tissue healing.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

RCS-01 therapy is safe and may improve skin structure by affecting gene expression.

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

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

BRG1 is essential for skin cells to move and heal wounds properly.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The B2C promoter works in sheep cells but not in mouse embryos.

ABCG2 protein marks stem-like skin cells in human epidermis.