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A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

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

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

Caffeine can protect scalp hair follicles from damage caused by UV radiation.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Apoptosis is essential for human skin development and forming a functional epidermis.

Lactate production is important for activating hair growth stem cells.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.