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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

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

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

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

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Regulatory T cells are essential for normal and improved wound healing in mice.

Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

Zinc supplementation may help improve treatment outcomes for chronic hepatitis C.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

The document concludes that patients with skin of color need specialized dermatological care and education to manage unique skin conditions effectively.

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

Different types of Armillaria fungus have a high genetic variety when partnering with Polyporus umbellatus mushrooms in China.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Lactate production is important for activating hair growth stem cells.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

α3β1-integrin is crucial for maintaining normal hair follicle shape and function but not needed for the development of the surrounding skin.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

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

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

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

Progesterone and its byproducts control a specific receptor in the brain independently of progesterone receptors, affecting conditions related to the menstrual cycle.