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Low testosterone in men is a risk factor for a specific heart rhythm issue, and testosterone treatment may help prevent it.

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

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

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

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.

Many women with hard-to-treat acne also have PCOS.

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

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

Researchers found two genes that may explain why some Casertana pigs don't have hair.

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.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Elevated CO2 can lessen the negative impact of water shortage on soybean roots and affects specific genes.

The document concludes that more research is needed to fully understand the causes of PCOS.

Scalp biopsies from dermatomyositis patients show chronic hair loss without scarring, with mucin and blood vessel changes being very common.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

FoxN1 overexpression in young mice harms immune cell and skin development.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

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.