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Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Sgk3 kinase is essential for normal hair growth in mice.

Mutations in hKAP1 genes may cause hereditary hair disorders.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

p63 controls Satb1 to help skin develop properly.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

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

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

AGC2-1 protein is essential for root hair growth in Arabidopsis.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

Stat3 affects skin cancer development by altering keratinocyte stem cell behavior.

PAR-1 may play a role in hair growth regulation in human hair follicles.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

PTCH gene mutations contribute to basal cell carcinoma development.

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.

A mix of specific inhibitors and a growth factor helps keep hair growth cells from losing their properties in the lab.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

H3K4me3 helps control RSPO3 to influence hair growth and development.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

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

Substance P helps restore skin thickness and cell renewal when sensory nerves are reduced.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.