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

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

The document concludes that targeting the androgen receptor may be a promising breast cancer treatment, especially for certain types.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Androgens play a key role in hair growth and disorders like baldness and excessive hairiness.

Different drugs can treat high male hormone levels in women, but they have various effects and some may harm a fetus.

Androgens play a role in female sexual function, and testosterone therapy can help women with low sexual desire, but more research is needed on treatments and long-term safety.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document concludes that pig iPSCs show promise for transplant therapies and the field is advancing in controlling cell behavior for biology and medicine.

PPAR agonists show promise for skin conditions but need more research before being a main treatment.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Protein microarrays are highly sensitive tools useful for disease diagnosis and studying proteins.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

The E2 protein affects gene activity in hair follicles of mice.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

Histone modification is key in treating chronic inflammatory skin diseases.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Hormones and metabolism play a complex role in prostate enlargement, and more research is needed to improve diagnosis and treatment.

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

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Epigenetic mechanisms control skin development by regulating gene expression.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.