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The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The humanized AA mouse model is better for testing new alopecia areata treatments.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Hsc70 protein may influence hair growth by responding to androgens.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

CD90 is present on specific cells in dog hair follicles.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

HLD10 can include increased body hair and Mongolian spots.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

CD90 is abundantly present on stem-like cells in dog hair follicles.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

HSPC016 gene is important for hair growth.

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

High levels of HSP70 and IL-15 are linked to more severe alopecia areata.

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.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.