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TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

RNase L suppresses regeneration in mammals.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Ptprq has multiple forms that change during inner ear development.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

Understanding snoRNA regulation may help slow skin aging.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

A new gene mutation linked to a skin condition was found in a Spanish family.

NLRP1 helps melanoma tumors grow by boosting inflammasome activation and reducing caspase-3 activity.

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

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Mutations in the KRT16 gene can cause skin and nail disorders.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Lack of KSR1 stops certain skin tumors in mice.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

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

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

PDRN is effective and safe for healing wounds and skin issues.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Loss of Rap1 protein speeds up heart aging in mice.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.