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The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

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

Blocking the ATX-LPA pathway may improve insulin sensitivity and mitochondrial function in obesity.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

A new hydrogel with stem cells from the human umbilical cord speeds up healing in diabetic wounds.

Nitric Oxide has potential in medicine, especially for infections and heart treatments, but its short life and delivery challenges limit its use.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Using Platelet-Rich Plasma and Adipose-Derived Mesenchymal Stem Cells together can improve healing, including wound healing, bone regeneration, and hair growth.

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.

Camellia japonica extract may improve scalp health and promote hair growth.

Selenium is essential for health, but too much or too little can cause problems; blood selenium levels are a good measure of intake.

Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Hair follicle development in cashmere goats involves dynamic changes in proteins and metabolites, with key roles for oxytocin, MAPK, and Ca2+ pathways.

Many women who have used performance-enhancing drugs in Finland show high rates of mental health and substance use issues, and most have normal red blood cell counts.

Taurine is important for many body functions and its deficiency can cause health problems.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Beta-blockers and anti-anginal medications have various side effects and interactions that require careful monitoring and individualized treatment.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

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

Anorexia and bulimia lead to serious health problems and increased risk of death, requiring aggressive treatment.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

Lamins are vital for cell survival, organ development, and preventing premature aging.