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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

CYP11A1 is crucial for skin health and disease by producing important steroids.

CYP2B12 enzyme in skin cells converts arachidonic acid into specific bioactive lipids.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Modulating Cytochrome P450 activity could help develop new skin disease treatments.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

Astilbin can potentially calm overactive immune responses, like in Type 1 Diabetes, by suppressing certain cell activities and reducing inflammation.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

New genes and pathways are important for testosterone production and male sexual development.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Early diagnosis and personalized treatment for PCOS are crucial, especially for young women in West Bengal, India.

Maternal exposure to artificial food coloring may increase skin disease risk in rat offspring.

The skin acts like an endocrine organ, making hormones that affect skin diseases and respond to stress.

Inhaled substances in e-cigarettes can cause hormone imbalances similar to congenital adrenal hyperplasia.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Polycystic ovary syndrome causes high male hormone levels, leading to symptoms like excess hair, acne, and fertility problems.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Botanical extracts from peas and chia seeds improved scalp health and protected hair from pollution.

Congenital Adrenal Hyperplasia is mainly caused by enzyme deficiencies, leading to varying symptoms like hormone imbalances and physical changes.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.