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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Researchers found two new genetic variants linked to Alzheimer's disease.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

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 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.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

A specific gene mutation causes a severe skin disorder in a family.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

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

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.