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Farudodstat may effectively treat alopecia areata without harming hair follicles.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

Ion-paired risedronate significantly increases skin penetration without irritation compared to risedronate alone.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

Farudodstat may help treat alopecia areata by protecting hair follicles.

DGAT1 enzyme is crucial for healthy skin and hair by regulating retinoid levels.

Basal cell carcinomas have much higher levels of Vitamin D3 receptors compared to healthy skin.

A rare gene variant causes hair and nail issues in a family.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Dutasteride potentially improves cell survival and reduces retinal damage in retinitis pigmentosa.

Certain hormone levels can help diagnose P450 oxidoreductase deficiency.

A sick foal with Rhodococcus equi pneumonia was successfully treated for multiple complications with targeted therapy and careful monitoring.

Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

PDRN is effective and safe for healing wounds and skin issues.

TCDD changes skin cell growth and keratin production in mice.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

Increased 11β-HSD1 activity in skin may contribute to aging and could be targeted to reduce aging effects.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

More awareness and education on iron deficiency anemia are needed in Riyadh.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.