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New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

Rat dermal papilla cells have unique genes crucial for hair growth.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Apoptosis is crucial for healthy skin and treating skin diseases.

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

Chemotherapy damages hair follicles, causing hair loss and other cellular changes.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

UV radiation causes skin cancer, but sunscreens and certain drugs can help prevent it.

Haplogroup X found in Altaian population supports Amerindian origin.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Dexamethasone speeds up hair loss in mice, while cyclosporin A slows it down.

Liposomes can safely and effectively deliver substances to mouse hair follicles, potentially useful for human hair treatments.

Cellular senescence has both cancer-blocking and cancer-promoting effects, and targeting senescent cells may improve health and lifespan.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Using two drugs together, Flutamide and 4-MA, is more effective for blocking male hormones than using each one alone.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Skin stem cells are maintained by signals from nearby cells and vary in their ability to renew and mature.

Male hormones control a specific gene in hamster skin, with different hormones having varying effects.

New technologies help us better understand how skin microbes affect skin diseases.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

MicroRNAs are crucial in controlling cell signaling, affecting cancer and tissue regeneration.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Visible light can damage skin and most sunscreens don't block it well; more research is needed on its effects and protection methods.

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

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