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Standardized procedures are crucial for collecting and preparing biological samples to ensure accurate clinical metabolomics results.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Chemical hair straighteners can cause scalp and hair damage, but long-term effects are unclear.

Microneedle therapy combined with serum effectively increases hair count in people with hair loss, with no side effects.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Nanomaterials can improve hair care products and treatments, including hair loss and alopecia, by enhancing stability and safety, and allowing controlled release of compounds, but their safety in cosmetics needs more understanding.

Cannabinoids like CBD and THC may help treat non-cancer skin diseases, but more research is needed.

A woman's hair loss led to discovering she had lupus.

Blocking DPP4 can potentially speed up hair growth and regeneration, especially after injury or in cases of hair loss.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Different genes are linked to various types of hair loss.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Anti-keratin antibody from cow milk makes damaged hair stronger and less likely to break.

The antibacterial toner can effectively kill acne-causing bacteria by penetrating skin plugs.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

A 2-year-old girl had a hair disorder not shared by her identical twin.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

The research found specific genes and pathways that control fur development and color in young American minks.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

New eco-friendly method strengthens and sets hair using light and causes less damage.