Search

everythinglearnresearchcommunity

for

Search:↓

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

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

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

CD2 might be a new treatment target for patchy alopecia areata.

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

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

The skin of both rat strains showed similar lectin binding patterns.

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

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

A specific gene mutation causes different hair defects in Indian monilethrix families.

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

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Researchers found a new mutation causing total hair loss from birth.

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

Scientists discovered two versions of a new human hair keratin gene.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

Vitamin D receptor and hairless protein are essential for hair growth.

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

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

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

HVDRR is caused by VDR gene mutations, leading to vitamin D resistance, treatable with high calcium doses, but alopecia remains permanent.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

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

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

Mutations in the hHb6 gene cause the hair disorder monilethrix.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.