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Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Scalp lesions in discoid lupus are more common in women and linked to other autoimmune diseases.

Human dermal γδT-cells respond to stress in hair follicles, contributing to hair loss.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

The hepatitis B vaccine did not cause hair loss in the tested mice.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

AR polyglycine repeat doesn't cause baldness.

A child's rare skin disease was triggered by chickenpox.

Innate lymphoid cells type 1 may contribute to alopecia areata by damaging hair follicles.

Alopecia Areata might be linked to Crohn's disease.

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

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Targeting the AhR pathway may help treat alopecia areata.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss in Discoid Lupus.

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

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.