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Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Deleting Crif1 in mouse skin disrupts skin balance and hair growth.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Electrochemotherapy successfully treated skin tumors in cats without recurrence.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Meis2 is essential for whisker development, independent of nerve involvement.

γδ T cells adapt uniquely to different tissues in mice.

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

Sheep have 17 keratin genes, similar to humans, but with different expression patterns affecting wool and hair.

Regulatory T cells are essential for normal and improved wound healing in mice.

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

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

Mouse models help understand alopecia areata and find treatments.

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

KY19382 helps regrow hair and create new hair follicles.

PTCH gene mutations contribute to basal cell carcinoma development.

Quercetin effectively treated and prevented hair loss in mice.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Activating PKCα in skin causes cell death and inflammation through different pathways.

Microneedle therapy combined with Hwangryeonhaedoktang solution improved hair growth in mice better than microneedle therapy alone.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

mTORC2 is crucial for healthy skin barrier by regulating lipids and filaggrin.