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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Ichthyoses are skin disorders causing scales, with treatment depending on type and severity.

ESR2 gene linked to female-pattern hair loss.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Experts met to improve care for ichthyosis patients in Spain.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

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

Genetic defects and UV radiation cause skin damage and aging.

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

Eicosanoids are crucial for skin health, and targeting their pathways may help treat skin conditions.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Understanding skin structure and development helps diagnose and treat skin disorders.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Certain fats in the skin help control inflammation and health, and changing these fats through diet or supplements might treat skin inflammation.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Using micro skin tissue columns improves skin wound healing and reduces scarring.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Testosterone therapy can help improve sexual desire and function in postmenopausal women but may cause side effects and is not FDA-approved for this use.