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Follistatin helps hair growth and cycling, while activin prevents it.

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.

After menopause, women lose a lot of skin collagen, but estrogen replacement might improve skin health.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Toxic epidermal necrolysis is a severe skin condition often caused by drugs, with complex treatment and a high risk of death, but survivors usually heal without scars.

Alopecia areata can cause unpredictable hair loss, and treatments like corticosteroids and minoxidil may help but have varying side effects.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Msx2 and Foxn1 are both crucial for hair growth and health.

The document concludes that accurate diagnosis is crucial for effectively treating common scalp disorders, which often have similar symptoms.

Cats with atopic dermatitis often have severe, year-round itching and respond well to certain treatments.

Mitoxantrone with a corticosteroid helps manage symptoms for some advanced prostate cancer patients but doesn't extend life.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Brain hormones significantly affect hair color and could potentially be used to prevent or reverse grey hair.

Oral retinoids can cause side effects ranging from mild to severe, including birth defects, and require careful monitoring and contraception.

The conclusion is that acne, alopecia, and hyperhidrosis are common skin issues with various treatments available, and accurate diagnosis is key for effective management.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Hair analysis for drugs needs a better understanding of how drugs enter hair, considering factors like hair structure and pigmentation.

People with late-stage HIV-1 often experience a specific type of hair loss linked to multiple factors, including nutritional issues and immune responses.

Topical immunotherapy, especially with DPCP, is effective for treating severe alopecia areata.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Hair treatments like bleaching increase friction by exposing tiny pores on the hair surface.

Different ethnicities and treatments affect human hair strength and structure.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Ketoconazole cream is effective for skin conditions like seborrheic dermatitis and may help with hair loss and other skin issues, with generally mild side effects.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Hair proteins have weak spots in their α-helical segments.