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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.

Finasteride works better for baldness in people with shorter gene repeats.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

The conclusion introduces a new way to classify skin cysts using their shape and genetic markers.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Reduced AR gene methylation may cause early pubic hair growth in girls.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Certain gene variations are not a major cause of male infertility in Nigerian men.

COVID-19 may worsen with androgens; anti-androgen drugs could help.

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

A new gene, JMJD1C, may affect testosterone levels in men.

Hair follicle stem cells are a promising source for tissue repair and treating skin or hair diseases.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Women with hair loss have more androgen receptors in certain hair follicles.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Epidermal stem cells show promise for future dermatology treatments due to ongoing advancements.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.