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Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Androgenetic alopecia involves genetics, hormones, and can be treated with medications or surgery.

The conclusion is that hair growth can be improved by activating hair cycles, changing the surrounding environment, healing wounds to create new hair follicles, and using stem cell technology.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The document concludes that the effectiveness of platelet rich plasma in aesthetic surgery is unclear due to inconsistent reporting and lack of objective measures in studies.

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

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Finasteride for hair loss may cause persistent sexual symptoms, depression, anxiety, and lower quality of life.

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

COVID-19 might affect male fertility, but more research is needed to understand the full impact.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

FLRG and follistatin have different roles in wound healing.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Feed restriction in sheep leads to finer wool fibers but may reduce wool quality.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

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

Certain microRNAs are more common in balding areas and might be involved in male pattern baldness.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

Calcium is important for stem cell function and maintenance, especially in blood and skin cells.

Hyaluronic acid-based HA2 hydrogel helps heal skin wounds better with less scarring.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.