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

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Fat-related cells are important for initiating hair growth.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Childhood obesity is rising globally due to various factors, and early prevention and healthy lifestyle changes are crucial.

Lgr5 is a marker for active, self-renewing stem cells in the intestine and skin, important for tissue maintenance.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

Anticancer drugs are increasingly found in surface waters, and their long-term environmental effects are not well understood, requiring better testing methods.

Hair regeneration needs dynamic cell behavior and mesenchyme presence for stem cell activation.

The circadian clock affects skin stem cell behavior, impacting aging and cancer risk.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Adult stem cells from rat whisker follicles can regenerate hair follicles and sebaceous glands.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

PCOS is a complex disorder in women that can lead to various health risks and requires personalized treatment.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

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.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Targeted cancer therapies often cause serious skin problems that need careful management.

The PDGF/PDGFR pathway is a potential drug target with mixed success in treating various diseases, including some cancers and fibrosis.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

Blocking COX, especially COX-2, in the skin can reduce inflammation and pain and may help prevent skin cancer.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.