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Women with non-classical congenital adrenal hyperplasia have higher levels of certain steroids, which can be reduced by treatment.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

Infliximab can cause SAPHO syndrome, which may improve with Spesolimab and methotrexate.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

TNFα and interleukin-1 blockers reduce skin inflammation from EGFR antibody therapy.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

VEGFR-2 activation is likely involved in hair follicle growth, survival, and development.

Keratinocyte growth factor promotes hair growth and reduces hair loss from chemotherapy.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Lrig1 could be a marker for advanced sebaceous carcinoma.

A unique case of skin cancer showed unusual calcification, possibly linked to calcium-binding proteins.

A patient with multiple sclerosis developed skin reactions after Daclizumab treatment, requiring more data on the drug's effects.

Increased Stat3 activity reduces hair follicle stem cells and boosts other stem/progenitor cells.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The treatment combining laser and fetal fibroblasts effectively reduces scarring.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

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

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

Longer treatment with vismodegib lowers relapse risk in basal cell carcinoma.

Recombinant Human Annexin A5 may help treat localized scleroderma by reducing skin thickening and inflammation.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

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