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Highly active but fewer CD14+CD16- monocytes are found in Alopecia Areata patients, regardless of severity.

An elderly woman with cancer improved after treatment for a rare skin condition with coiled hairs.

Most children with skin inflammation taking methotrexate had lab abnormalities, but liver issues often improved without changing the medication dose.

Early diagnosis and proper treatment improve outcomes for methylmalonic acidemia.

A potential genetic link between Werner syndrome and kidney disease was suggested.

Immortalized hair follicle cells could be useful for regenerative medicine and treating inflammation and oxidative stress.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Glioblastoma cells can make androgens, which might help the tumor grow.

The 2012 criteria are better for diagnosing atypical lupus cases.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

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

A boy had a rare scalp condition with thickened skin and different-colored hair.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Lupus can be a rare cause of high calcium levels in the blood.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

Immunological treatment improved both neuropathy and alopecia.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

Lack of a certain enzyme causes hair to grey early by damaging stem cells, but an antioxidant can help prevent this.

Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

Werner's syndrome causes early aging and increases cancer risk, requiring early diagnosis and symptom management.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

MEX3A is crucial for maintaining intestinal stem cells in mice.