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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.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

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

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

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.

A gene variation is linked to hair thickness in Asians.

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

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

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

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

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.

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

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.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

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.

A woman with severe hair loss was successfully treated with the drug adalimumab.

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

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.