Search

everythinglearnresearchcommunity

for

Search:↓

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

The enzymes 5α-reductase and 3α/β-hydroxysteroid oxidoreductase help create brain-active substances from progesterone and testosterone, which could be used for treatment, but more research is needed to ensure their safety and effectiveness.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

No link found between specific genes and female pattern hair loss.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Hair follicle regeneration may slow tumor growth.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Manage side effects of hepatitis C treatment with dose changes and medications, which may improve patient adherence and treatment success.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Overexpressing Tβ4 in goats' hair follicles increases cashmere production and hair follicle growth.

Diagnosing hyperandrogenism in women is complex and requires accurate testing methods and consideration of SHBG levels.

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

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

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

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Sorafenib can cause facial acne-like eruptions, which improve after reducing the dose or stopping the drug.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Embryonic and adult stem cells are valuable for improving skin grafts and cell therapy.

Gene differences may affect baldness treatment response in Korean men.

The document concludes that treatments for female hair loss and excessive hair growth are temporary and not well-studied.

Thai rice bran extracts, especially from Tubtim Chumphae rice, can significantly reduce the activity of hair loss genes, with x-tocopherol showing potential as an anti-hair loss product.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.