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The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Lifestyle factors like BMI at young adulthood can increase cancer risk in women with Lynch Syndrome, but diet and height don't seem to affect this risk.

STK11 gene polymorphism does not predict metformin response in PCOS.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Certain variations in the vitamin D receptor gene are linked to an increased risk of polycystic ovary syndrome.

Birth control pills change the activity of certain inflammation and blood clotting genes in women with PCOS.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

Short photoperiods improve cashmere growth and quality in goats by changing hormone levels and gene expression.

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.

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

Doctors need more training in skin cancer screening, a new treatment is effective for a skin condition, better diagnosis methods for skin cancer are available, hair loss in women may be linked to hormones and cholesterol, certain skin care products might cause hair loss, babies' skin gets weaker after birth, and a gene mutation might be linked to eczema.

Scientists created a new 3D skin model from cells of plucked hairs that works like real skin and is easier to get.

A new non-invasive method can analyze skin mRNA to understand skin diseases better.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

New technologies in acupuncture and biosensors show promise for better medical treatments and healing.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Improving artificial vascular grafts requires better materials and surface designs to reduce blood clotting and support blood vessel cell growth.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Skin aging is due to impaired stem cell mobilization or fewer responsive stem cells.

The document concludes that understanding hair follicle cell cycles is crucial for hair growth and alopecia research, and recommends specific techniques and future research directions.

Sex hormones, especially estradiol, can change chicken feather shapes and colors.