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Researchers developed promising agents for prostate cancer imaging, with the best one showing high potential for clinical use.

Keratose, derived from human hair, is a non-toxic biomaterial good for tissue regeneration and integrates well with body tissues.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Asia has made significant progress in tissue engineering and regenerative medicine, but wider clinical use requires more development.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

EDA2R gene linked to hair loss.

Human skin cells produce proenkephalin, which changes with environmental factors and skin diseases.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

SAHA syndrome is a condition in women involving skin and hair issues, often related to hormonal imbalances, and is treated based on the underlying cause.

Advanced hydrogel systems with therapeutic agents could greatly improve acute and chronic wound treatment.

Korean Red Ginseng has beneficial components that help with stress, immunity, fatigue, memory, blood flow, and disease protection.

Red ginseng may improve immunity, fatigue, memory, blood circulation, and menopausal symptoms, and is generally safe to consume.

Macrophages are vital for skin healing, hair growth, salt balance, and cancer defense.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Scientists found a gene in mice that causes early hearing loss.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Chemokine signaling is important for hair development.

Finasteride helps treat hair loss and prostate enlargement by blocking a specific enzyme.

Manatee whiskers are specially adapted for touch in water.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Blocking the prolactin receptor might help treat various diseases, but more research is needed.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.