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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

Relapsing hepatitis A can cause prolonged abnormal liver tests even without symptoms.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

DDR-II hair follicle cells don't respond to 1, 25-dihydroxyvitamin D3, aiding diagnosis.

A girl developed vitiligo and psoriasis after hepatitis B treatment, and stopping the treatment didn't help.

DM and AA may share a common cause.

CD4 T cells need IFN-γ to cause hair loss in alopecia areata.

Mutations in the LIPH gene cause woolly hair in a child.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

Plasmacytoid dendritic cells, which overproduce IFN-α, may play a crucial role in starting alopecia areata, an autoimmune disease causing hair loss.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Gamma/delta T cells help defend skin against heavy metals.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

RXRα is crucial for proper immune response and links diet to immune function.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

Farudodstat may help prevent hair loss in alopecia areata by stopping immune attacks on hair follicles.

CD8+ T cells re-expressing CD45RA may predict treatment resistance in severe alopecia areata.

Dermoscopy helped diagnose discoid lupus erythematosus in two patients without needing skin biopsies.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

A man got six skin cancers within a year after a cell transplant for leukemia but was cancer-free 32 months later; skin checks are important post-transplant.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Hispanic patients in the USA have lower survival rates for melanoma compared to non-Hispanic Whites.