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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

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

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Reduced AR gene methylation may cause early pubic hair growth in girls.

UBC13 and UBC22 enzymes are important for plant growth and development in Arabidopsis thaliana.

TPA promotes hair growth by increasing stem cell activity and activating specific cell signals.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

HPV infection is linked to better survival in advanced anal cancer, higher radiation doses improve survival, especially in HPV-negative patients, and prostaglandin E₂ pretreatment can protect mouse hair follicles from radiation damage.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

MYB30 and EIN3 work against each other to control root hair growth and phosphorus uptake in plants when phosphate is low.

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

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

PROTACs show promise in cancer treatment by effectively degrading specific harmful proteins.

Gene variation affects prostate issues and hair loss.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

PPAR-γ signaling improves mitochondrial function in hair follicles, potentially affecting hair growth and aging.

Accurate protein modeling can help develop new treatments for prostate cancer and other diseases.

Mutations in the SNRPE gene cause hereditary hair loss.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

Compound 6 is a promising candidate for better wound healing.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.