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

A rare gene variant causes hair and nail issues in a family.

The Eda gene helps regulate the hair cycle in goats.

BMPR1a-ECD reduces wrinkles much more effectively than retinoic acid.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

PDRN helps repair tissue and improve wound healing with a high safety profile.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Niacin deficiency makes rats more sensitive to cancer-causing chemicals.

A new nanocage system protects hair cells and reduces hearing loss effectively.

A20 protein is crucial for normal skin and hair development.

17β-estradiol boosts APE1/Ref-1 secretion in cells and mice via a calcium-dependent pathway.

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.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Ptprq has multiple forms that change during inner ear development.

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

A gene mutation causes curly hair and hair loss in rats.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.