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Mice with human skin protein K8 had more skin problems and cancer.

Significant progress was made in understanding PXE, but effective treatments are still needed.

The document suggests creating a validated score to diagnose Cushing's Syndrome and considers plasma steroid profiling as a simpler diagnostic method.

A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

Macrophages help hair growth after injury through CX3CR1 and TGF-β1.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

People with Down's syndrome often have more skin problems due to a weak immune system.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Polycystic ovary syndrome (PCOS) lowers women's quality of life, especially mentally and socially, but nursing guidelines can improve their understanding of the condition.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A specific immune response helps control mite populations on the skin, maintaining healthy hair follicles.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Stem cells are crucial for wound healing and understanding their role could lead to new treatments, but more research is needed to answer unresolved questions.

Women with PCOS are more likely to have impaired glucose tolerance and type 2 diabetes, especially if they are Asian or obese.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

CDP is crucial for lung and hair follicle cell development.

Stem cell niches support, regulate, and coordinate stem cell functions.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

Exosomes could potentially enhance tissue repair and regeneration with lower rejection risk and easier production than live cell therapies.

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

New treatments targeting specific genes show promise for treating keratin disorders.

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

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Different body areas in mice produce different hair types due to interactions between skin layers.