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The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Oral antiandrogens effectively treat female hair loss, with better results in higher hair loss grades.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Researchers identified genes and proteins that may influence wool thickness in sheep.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

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

Hair follicles offer promising targets for delivering drugs to treat hair and skin conditions.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

A specific gene mutation causes congenital hair loss.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

No clear link between androgen receptor variation and hair loss, but more research needed.

Vitamin A may influence hair loss conditions like alopecia, but more research is needed to understand how.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Father's finasteride use may affect son's fertility and testicular function.

A gene mutation in Lama3 is linked to a common type of hair loss.