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A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Microsporum gypseum fungus breaks down keratin in hair by digesting it enzymatically, starting with less keratinized parts.

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

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

A new diagnostic model can help better diagnose and understand Alopecia Areata.

Four antibodies were developed to help study hair follicle cell differentiation.

MOF controls skin development by regulating genes for mitochondria and cilia.

Blocking autophagy worsens lipid buildup and dysfunction in brain cells after injury.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

Steroid injections improved symptoms and hair regrowth in a woman with a reaction to permanent makeup.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

Basement membrane supports fibroblast aggregation, aiding hair follicle development.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Gamma/delta T cells help defend skin against heavy metals.

MMP-9 increase in hair follicles may lead to hair loss.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Increased cell death and reduced cell growth in hair follicles contribute to baldness.

The research suggests that immune cells and a specific type of cell death called ferroptosis are involved in Frontal fibrosis alopecia.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

The modified osmium method improves hair cortex staining for better visualization.

Certain astrocytes can protect the brain and improve recovery after a stroke, and a hair loss drug might reduce cancer spread.

Progesterone affects GABA_A receptor function by altering δ subunit levels.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.