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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

MC-1R in skin cells may influence inflammation and collagen production.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

Lower MC2R expression may contribute to alopecia areata.

BRG1 is essential for skin cells to move and heal wounds properly.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

MPA increases cancer spread by boosting Eph A2 activity.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.