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Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Women with PCOS may take longer to get pregnant but can have a normal family size, and should manage their overall health to reduce long-term health risks.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

Androgen therapy can help with symptoms like low libido in women, but more research is needed to understand its long-term safety and effects on health.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Non-immune factors play a significant role in alopecia areata.

Bone marrow and umbilical cord stem cells can help grow new hair.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

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

Human hair loss may have evolved to help increase brain size.

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

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Bald areas have lower cell growth, more DNA damage, and increased cell death.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

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

Wnt3a activates certain genes in hair follicle cells, including a newly discovered one, EP2, which may affect hair growth.

Bioluminescence imaging can track hair follicle cells and help study hair regrowth.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Androgens and a high-fat diet may increase the risk of severe COVID-19 in women with PCOS by upregulating certain proteins in the heart and kidneys.

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

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.