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Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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

A specific gene mutation causes woolly hair and hair loss.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

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

A specific DNA region controls skin cell gene expression by working with certain proteins.

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Keratin 14 is uniquely found in a specific group of placental cells.

KRTAP6 genes affect wool quality in sheep.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

The 4C32 gene may help in mouse skin development and differentiation.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

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 genetic region, 17q21.31, is linked to higher ovarian cancer risk.

New compounds may help treat heart disease by activating specific potassium channels.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

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