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Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

Many people diagnosed with androgenic alopecia might actually have hidden scarring or inflammation.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Diabetes causes lasting cell dysfunctions, leading to serious complications even after blood sugar is controlled.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

The patient showed signs of liver disease due to alcohol use but didn't need treatment for Dupuytren’s contracture.

The newborn's skin condition improved over time, leaving only lighter skin patches.

Defective repair processes may cause immune activation and inflammation in psoriatic disease.

The document concludes that using gadolinium-based contrast agents during MRI can be linked to Nephrogenic Systemic Fibrosis in patients with severe kidney disease.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Chemotherapy causes hair loss by damaging hair follicles and stem cells, with more research needed for prevention and treatment.

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

Long-standing benign tumors can become cancerous, especially in people with weakened immune systems.

Other common signs, not just the well-known immune cells around hair bulbs, are important for diagnosing hair loss from alopecia areata.

Polyamines help fix DNA damage accurately in cells.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Treatment can improve survival and symptoms in dogs with Cushing's disease, but outcomes are unpredictable.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

The authors suggest that a new type of hair loss exists, which is different from alopecia areata.

Immune checkpoint inhibitors used in cancer therapy can cause hair loss, and understanding this can help manage the side effect.

Alfredo Rebora suggests a simpler classification for hair loss and a new test for easier diagnosis.

Cyproterone helps women with hair loss caused by genetics. More research is needed to confirm the best dose.

Micro-CT helps identify suitable areas for surgical procedures based on blood vessel distribution in hypospadias-affected rats.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Dissecting cellulitis may have genetic links and can cause permanent hair loss.