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Genetic factors and diet significantly increase the risk of male pattern baldness.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

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

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

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

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

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

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

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

Men who start balding at age 20 may have a higher chance of getting aggressive prostate cancer.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

CT60 polymorphism might increase the risk of Alopecia Areata.

Certain gene variations may increase the risk and severity of alopecia areata.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

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.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

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

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Certain gene variations are found in people with polycystic ovary syndrome.

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

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

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.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.