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Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

SOX4 is crucial for the development of melanoma.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The PML protein helps prevent skin cancer in mice.

Blocking mTORC1 reduces skin tumor growth in mice.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

ABCG2 protein marks stem-like skin cells in human epidermis.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A gene mutation causes monilethrix in a Chinese family.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

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

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

A new mutation in the HR gene causes hair loss in a specific family.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

NDP-MSH protects brain cells and reduces inflammation in Parkinson's disease by activating MC1R and involving Tregs.