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A rare case shows a possible link between Neurofibromatosis type 1 and Becker nevus due to genetic mutations.

Activated β-catenin affects hair growth and skin thickness, and changes are reversible.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

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

ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes that lead to more hair follicles entering resting phases.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Male rats have more somatostatin neurons than females due to testosterone converting to estrogen during early development.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

ZNF750 helps keep hair follicles healthy and prevents skin inflammation.

AP-1 controls tumor cell type by affecting key signaling pathways.

Fibronectin is essential for hair follicle regeneration by supporting stem cells.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

PP2Acα is essential for proper hair and skin development.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

Notch signaling is crucial for specifying niche cells in Drosophila testis.

Nestin-expressing progenitor cells become outer root sheath keratinocytes.

Targeting NCoR1 can help treat heart enlargement and dysfunction.

Nfib in hair follicle stem cells boosts melanocyte stem cell growth and differentiation.