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Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

CD98hc's role in skin health decreases with age.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Researchers can now observe live cell processes in the Drosophila midgut for extended periods.

FoxN1 overexpression in young mice harms immune cell and skin development.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

IL-1 receptor absence in mice leads to skin cysts and changes in immune response after UVB exposure.

Alk1 in specific cells is crucial for proper nerve branching and hair function.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Versican in dermal papilla cells is crucial for healthy hair growth.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

ALX4 is crucial for normal craniofacial and hair development, with specific roles in different cell types.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Testosterone reduces key molecules needed for early pregnancy in rats.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

FoxN1 gene is crucial for proper thymus structure and normal skin appearance.

Cannabidivarin (CBDV) may help brain cell growth and survival through the TRPV1 receptor.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.