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IL-17 and certain immune cells are linked to more severe alopecia areata.

FMF and mycosis fungoides are variants of the same disease, and bexarotene can be an effective treatment.

A new patch can deliver stable antibodies over time for potential HIV treatment.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Blocking IL-12 can help treat alopecia areata by preventing hair follicle immune issues.

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

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.

Melanocytes may trigger the immune response in alopecia areata, affecting hair regrowth.

A gene mutation causes monilethrix in a Chinese family.

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

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

MCHR2 gene duplications may be linked to alopecia areata.

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Somatostatin may help protect hair follicles from immune attacks.

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

Two main types of fibroblasts with unique functions and additional subtypes were identified in human skin.

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

Expanded CD8+ T cells are linked to Alopecia Areata and may cause relapse after treatment.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.

Enhancing Tregs can protect against alopecia areata.

The new Hairless R/J mice model improves imaging for tumor monitoring and cancer therapy evaluation.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

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

Some brain cancer cells avoid immune system detection, and certain treatments could target this to slow their growth; also, certain fat cell precursors help regenerate hair and skin after injury.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Specific keratin gene mutations can cause monilethrix.