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Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

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

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

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

UV light helped human hair transplants survive in mice without broad immunosuppression.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

The Fas/FasL pathway may play a role in alopecia areata.

Vδ1+ T-cells in the skin contribute to hair loss in alopecia areata and could be targeted for treatment.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Trichohyalin in hair can trigger immune attacks in alopecia areata.

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

A man developed facial skin lesions after a stem cell transplant, which improved with specific treatments.

TH antibodies in vitiligo and AA patients recognize the same protein parts.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Blocking the CCR5 receptor may be a new way to treat hair loss from alopecia areata.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

CT60 polymorphism might increase the risk of Alopecia Areata.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.