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Blue-light activation of TrkA improves hair-follicle stem cells' ability to become neurons and glial cells.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Three genes in Arabidopsis are important for plant growth and development by affecting sugar attachment to proteins.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Hoxc genes control hair growth through Wnt signaling.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

Human thymus has stem cells that can self-renew and maintain their identity.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

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

The hHa7 gene is regulated by androgens in certain body hair, not scalp hair.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

CCC1 is essential for ion balance and proper plant cell function.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Dynlt3 is important for melanosome transport and skin coloration.