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Immune checkpoint inhibitors can increase the risk of autoimmune skin diseases, especially bullous pemphigoid.

Hair follicles help skin immune recovery after UVB exposure.

Activating TLR5 in the gut can extend lifespan and improve health in aged mice.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

COVID-toes show a unique immune response over time, different from vaccine-related chilblains.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

Anifrolumab significantly improved skin lesions and hair regrowth in severe discoid lupus.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

The study identified key immune cell differences between mild and severe alopecia areata.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Two microRNAs affect hair follicle development in sheep by targeting specific genes.

Double stranded RNA helps skin wounds heal by coordinating specific proteins and signaling pathways.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

p120-catenin helps control skin inflammation by regulating cadherin levels.

FGF13 gene changes cause excessive hair growth in a rare condition.

CDP is crucial for lung and hair follicle cell development.

CLEC10A and interleukin-42 can help identify PCOS patients' response to Metformin treatment.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Oral tofacitinib can treat both psoriasis and alopecia universalis by normalizing inflammatory pathways.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Dandruff is linked to changes in the immune system of hair follicles and skin.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

DNA methylation changes are linked to skin diseases with inflammation.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.