Search

everythinglearnresearchcommunity

for

Search:↓

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Alopecia areata patients have higher levels of IL-6 and TNF-α.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Alopecia areata and vitiligo share immune system dysfunction but differ in specific immune responses and affected areas.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Case-only trees and random forests improve predictions of treatment effects in clinical trials.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.