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Early hair loss in men may signal broader health issues similar to PCOS in women.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Women with PCOS face higher risks of diabetes and heart disease, and these risks increase with obesity.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Men can have genetic risks for PCOS-related traits like obesity and diabetes.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

AR polyglycine repeat doesn't cause baldness.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

The free androgen index varies among women with different types of PCOS.

Burn scars form abnormally due to changes in wound healing, and more research is needed to improve treatments.

Polycystic Ovary Syndrome (PCOS) symptoms vary globally, with bloating, high cholesterol, and glucose levels being common; the current diagnostic criteria may need refining.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Magnesium oxide-infused membranes help heal wounds faster by reducing inflammation and promoting skin and hair follicle growth.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

Regulatory T-cells are important for healing and regenerating tissues in various organs by controlling immune responses and aiding stem cells.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Hyaluronic acid increases collagen synthesis safely, while poly-L-lactic acid may cause complications by affecting fibroblasts.

Trichoscopy helps detect early complications in hair transplants and ensures quality in the procedure.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A new gene variant causes glucocorticoid resistance in a mother and son.

Careful light microscopy is crucial for detecting mild cases of pili annulati, which weakens hair and varies widely in expression.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.