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K39 and K40 are the last keratins expressed in hair development, completing the hair keratin catalog.

A new gene mutation causes a rare type of hair loss.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

The Apc gene is crucial for normal skin and thymus development.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

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

TRPV3 in skin cells causes inflammation and cell death.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

A specific gene mutation causes long hair in Angora rabbits.

Markers CRABP1, Nestin, and Ephrin B2 are present in skin cancer environments and may influence their development.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Some hair proteins are specific to hair, while others are also found in skin cells.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

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

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.