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

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

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

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Nociplastic type pain, common in Chronic Overlapping Pain Conditions, is a complex, heritable trait linked to 24 unique genetic factors and 127 genes, with potential shared mechanisms in cognitive, personality, and metabolic traits.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

A genetic variant linked to hair thinning in Japanese women was found.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

DNA analysis can help tailor alopecia treatment.

Early onset female hair loss is linked to lower hair density, scalp issues, and certain genetic factors.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

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.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Certain genes may influence hair loss differently in men and women.

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

Some early COVID-19 mutations in patients predicted future common virus mutations.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Certain IL-18 gene variations may increase the risk of alopecia areata.