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

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

Researchers found a genetic region that influences the number of coat layers in dogs.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

The ZIP13 variant is linked to abnormal hair quality.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Sciellin is a protein that helps form protective layers in skin, hair, and nails.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

The Wave complex controls skin growth by suppressing certain signals.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Krox20 is crucial for hair growth and maintaining skin stem cells.

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

A new tool accurately identifies human cornea cell states and key factors.

The EDA pathway plays a key role in bone development by interacting with other signaling pathways.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Dopaminergic neurons in the gut have distinct subtypes, some releasing both dopamine and acetylcholine.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Overexpressing CtBP1 in skin cells causes skin and hair problems.