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The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A man with testotoxicosis was fertile despite low FSH levels, suggesting high testosterone may allow sperm production without FSH.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

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

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 chapter explains the causes of excessive hair growth and masculinization in women and how to measure hormone levels related to these conditions.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

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

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

The document concludes that alopecia areata is an unpredictable autoimmune hair loss condition with no cure, but various treatments exist that require personalized approaches.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

Review finds no permanent solution for female hair loss.

Review determines effective, safe treatments for female hair loss.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Alopecia areata causes hair loss with varied treatment responses and frequent relapses.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

A specific genetic deletion in goats affects cashmere yield and thickness.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Addressing underrepresentation in Parkinson's research is crucial for better treatments and understanding.

Air Vice-Marshal Sir Ralph Jackson significantly advanced dialysis technology in the UK.

Vitiligo is often found with other autoimmune diseases, which is important to know to help patients.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.