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In Italian patients with lupus, the most common skin issue was chronic cutaneous lupus, especially discoid lesions, and nonspecific skin problems occurred in about a third of those with systemic lupus, mainly during active disease.

Probiotic bacteria improved skin and hair health in aged mice.

The conclusion is that FFA and LPP have similar scalp biopsy features, making them hard to distinguish histologically, and FFA may be a specific kind of scarring hair loss.

The document describes how to tell different types of non-scarring hair loss apart by looking at hair and scalp tissue under a microscope.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

New treatments targeting specific genes show promise for treating keratin disorders.

The document concludes that hair is complex, with a detailed growth cycle, structure, and clinical importance, affecting various scientific and medical fields.

Researchers found that hair shedding happens mostly when new hair is growing and involves a unique process.

The document concludes that proper diagnosis and a combination of medical, hair-care, and surgical treatments are important for managing alopecia in black women.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

No treatment fully prevents hair loss from chemotherapy yet.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Hair elemental analysis could be useful for health and exposure assessment but requires more standardization and research.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Grafted rodent and human cells can regenerate hair follicles, but efficiency decreases with age.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Trichoscopy helps diagnose and monitor alopecia areata by looking at a combination of specific hair and scalp features.

Using nanostructured lipid carriers to deliver spironolactone could improve treatment for hair loss.

Targeted cancer therapies often cause skin reactions, so dermatologists must manage these effects.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mutant mice help researchers understand hair growth and related genetic factors.

Mannosylerythritol lipids are good for skin and hair care products.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

Hair shedding is an active process that could be targeted to treat hair loss.

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.

Chitosan nanoparticles improve minoxidil delivery to hair follicles for better alopecia treatment.

A20 protein is crucial for normal skin and hair development.