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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Certain immune cells may cause hair loss by reacting to stressed hair follicles.

miR-200c-3p could help diagnose and treat alopecia areata.

A patient with advanced kidney cancer and no hepatitis C developed skin inflammation due to a drug called interferon alpha-2a.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Trichohyalin in hair can trigger immune attacks in alopecia areata.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Hsc70 protein may influence hair growth by responding to androgens.

High DKK1 levels predict worse survival in head and neck cancer.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Human Beta Defensin 1 levels do not predict the risk or severity of Alopecia Areata.

BIVV009 is a safe treatment for bullous pemphigoid that reduces C3 deposition without harmful side effects.

Dandruff is linked to changes in the immune system of hair follicles and skin.

EDA2R gene linked to hair loss.

Targeting IL-15 may help treat Alopecia Areata.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

The study identified key immune cell differences between mild and severe alopecia areata.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

KLHL24-mutant stem cells help understand skin and heart disease.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.