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The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

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

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

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

Male pattern hair loss may be linked to the developmental origins of hair follicles.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Minoxidil may work for hair loss by reducing androgen sensitivity and altering hormone-related enzymes.

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

Estrogens generally inhibit hair growth and improve skin quality, but their exact effects on hair follicles are complex and not fully understood.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

DHT, a testosterone byproduct, causes male pattern baldness.

Iron deficiency might contribute to hair loss in women.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Certain gene variations might be linked to severe acne in women but not in men.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.