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The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

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

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Haplogroup X found in Altaian population supports Amerindian origin.

Some people have a genetic variation that makes them less effective at breaking down drugs.

CT60 polymorphism might increase the risk of Alopecia Areata.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

A gene variation is linked to hair thickness in Asians.

Lymphatic vessels are essential for hair follicle growth and skin regeneration.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Gene differences may affect baldness treatment response in Korean men.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

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

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Certain gene variations may increase the risk of hair loss in Egyptians.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

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