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

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

IL-19 and IL-24 help cells respond to DNA damage and could be targeted for cancer and age-related disease treatments.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

Lipase H is important for hair follicle function and shaping hair fibers.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

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

Scientists found out how a specific protein in human hair cuticles behaves and is structured.

Hairless protein can block vitamin D activation in skin cells.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

H3K4me3 helps control RSPO3 to influence hair growth and development.

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

A specific gene mutation causes congenital hair loss.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

PP405 may help hair growth by activating hair follicle stem cells.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

K6hf is a unique protein found only in a specific layer of hair follicles.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Tph cells are linked to the severity of systemic lupus erythematosus.