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Cell division orientation varies by body site and is linked to epidermal thickness and cell density.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

Switching flying squirrels' diet from seeds to mouse chow restored their hair.

Human prostate cells produce more WISP1/CCN4 when there's not enough oxygen.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

Wnt-signaling is regulated differently in skin cells and immune responses during wound healing.

Overactive Stat3 in mouse skin causes hair loss and cell structure damage.

KY19382 speeds up wound healing by activating a specific cell signaling pathway.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A wireless, battery-free system uses Wi-Fi signals to enhance wound healing and enable smart healthcare at home.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Hair patterns in mice are controlled by both a global system dependent on Fz6 and a local self-organizing system.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Both genetic and hormonal factors are crucial for bird sex differentiation, and disturbances can cause sex reversal.

Researchers created a fully functional, bioengineered skin system with hair from stem cells that successfully integrated when transplanted into mice.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Slug (Snai2) helps regulate hair growth timing in mice.

A gene mutation in Lama3 is linked to a common type of hair loss.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

NLRP3 helps control inflammation and repair in wound healing, making it a potential target for treatment.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.