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A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Hair growth and health are influenced by factors like age, environment, and nutrition, and are controlled by various molecular pathways. Red light can promote hair growth, and understanding these processes can help treat hair-related diseases.

Women's hair loss can be due to hormonal changes and various conditions, with treatments focusing on stopping progression and managing symptoms.

Skin aging reflects overall body aging and can indicate internal health conditions.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Disrupting Smad4 in mouse skin causes early hair follicle stem cell activity that leads to their eventual depletion.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Disrupting Stat3 in hair follicle stem cells greatly reduces skin tumor formation.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Finasteride can cause lasting sexual dysfunction, depression, and other side effects, needing more research for treatment.

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

Genetic defects and UV radiation cause skin damage and aging.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Changing allopregnanolone levels in baby rats affects their adult behavior and alcohol use.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Cocaine impairs male sexual behavior and alters testosterone metabolism in the brain.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

The skin's internal clock affects healing, cancer risk, aging, immunity, and hair growth, and disruptions can harm skin health.