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Studying rare genetic disorders can help us understand and treat common diseases better.

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

The study suggests that changes in immune system receptors and their interaction with a cell component may be important in the development of a type of hair loss condition.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

TRPS1 is crucial for bone, kidney, and hair follicle development.

TSPO might help treat anxiety and depression.

Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Calcium blockers may help prevent hearing loss by protecting hair cells.

Corin helps control salt and sweat release in sweat glands.

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

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

μ-opiate receptors in skin cells may affect skin health and healing.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

The combined treatment effectively managed severe skin issues in Olmsted syndrome.

Vitamin D3 and its receptor help protect skin from UVB-related cancer.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

Solute binding to hair keratin is mainly driven by hydrophobic interactions and changes with pH.

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.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Dopaminergic neurons in the gut have distinct subtypes, some releasing both dopamine and acetylcholine.

Vitamin D receptor helps prevent skin tumors.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

Vitamin D receptor may help protect against UV-induced skin cancer.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

New compounds similar to cromakalim were less effective at inhibiting insulin release but improved in solubility and one acted as a calcium entry blocker, not a potassium channel opener.