Search

everythinglearnresearchcommunity

for

Search:↓

A woman's hair loss and skin discoloration were found to be caused by a rare case of leprosy on the scalp, not alopecia-vitiligo overlap.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Nucleic acid polymers can enhance antiviral responses and improve treatment outcomes for chronic hepatitis B.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A woman with lupus had blood cell destruction, treated successfully with medication.

Lichen planus commonly affects middle-aged adults, often involves limbs and mucosal areas, and can be linked to immune diseases.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

A gene mutation in mice causes permanent hair loss and skin issues.

Higher IL-37 levels are linked to more severe alopecia areata, but the gene variation doesn't affect disease risk.

The dense fine speckled pattern in ANA tests is common in autoimmune diseases, challenging previous beliefs that it was unrelated.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Certain gene variations are linked to alopecia areata.

People with celiac disease have a higher risk of developing alopecia areata.

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

Two specific genetic markers increase the risk of hair loss in Asian populations.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Higher IL-17A and IL-23 levels are linked to alopecia areata severity and could help in tracking and treating the disease.

Both Th1 and Th2 immune responses are increased in alopecia areata, with Th2 response more strongly linked to how severe the disease is.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

Increased Toll-like receptors in blood cells may contribute to alopecia areata and could be a target for new treatments.