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New genes and pathways are important for testosterone production and male sexual development.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Malnutrition severely harms growth and development in young baboons.

Nonantibiotic macrolides show promise for treating various inflammatory skin conditions.

Testosterone is crucial for development, growth, and various body functions in mammals.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

Eclipta alba has many health benefits and contains compounds with potential for drug development.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Finasteride, when given in high oral doses to pregnant monkeys, caused genital abnormalities in male fetuses, but not in female fetuses or those exposed to intravenous finasteride.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Severe acne in a young girl may indicate underlying hormonal issues.

Most pregnant women experience skin darkening and hair changes, with these effects usually going away after giving birth.

Neuregulin3 affects cell development in the skin and mammary glands.

A hair tightly wrapped around a toddler's toe caused severe crying and was treated by surgery.

Hair is a complex organ, and understanding its detailed structure and growth phases is crucial for analyzing substances within it.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Natural herbal compounds might treat certain medical conditions by reducing DHT levels, but more research is needed to confirm their effectiveness and safety.

D-004 may be a natural alternative to finasteride for treating enlarged prostate and male baldness.