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Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Scarring alopecia affects different hair follicle stem cells than nonscarring alopecia, and the infundibular region could be a new treatment target.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Mutations in the KRT85 gene cause hair and nail problems.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The composition with carnitine, thioctic acid, and saw palmetto extract may effectively reduce inflammation in hair follicle cells.

Telogen is an active phase with important biological processes, not a resting phase.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

No link found between aromatase gene and female hair loss.

Finasteride side effects in young men may be linked to specific gene variations.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Certain gene variations are linked to better memory in healthy Chinese women.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Different body parts have varying levels of certain hair follicle markers.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.