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UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Certain genes can predict how well breast cancer patients respond to chemotherapy.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

Common Black hair care products may affect hormone levels and potentially impact health, especially in reproductive and metabolic areas.

Acetate helps reduce depression in rats with PCOS by lowering specific gene expression and DNA changes in the brain.

Key genes and pathways influence cashmere production in goats.

Genetic variants in specific genes cause a type of hair loss.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.

Mice with human gene experienced hair loss when treated with DHT.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Goat skin has more keratin genes, while the mammary gland has more immunity-related genes.

Prostate cancer is common, but risk can be reduced by avoiding smoking, unhealthy diet, inactivity, certain medications, and risky jobs.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Androgenetic alopecia is a common genetic and hormonal hair loss affecting many men and women.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

Alopecia is common in severe cases of autosomal recessive congenital ichthyosis.

SARS-CoV-2 may worsen IPF due to shared genes and pathways, suggesting potential drug targets.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

Bee venom helps hair grow and may work better than some common treatments.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.