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Different types of atopic dermatitis were linked to specific genetic and immune changes, suggesting that severe cases might need stronger immune-targeting treatments.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Glycerol may improve wound healing and prevent keloids, a device can measure itch intensity, male pattern baldness is highly heritable, and fumaric acid esters may work for psoriasis by causing cell death in T cells.

Cross-section trichometry is an accurate method to measure hair loss and growth.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Hypothyroidism may cause certain types of hair loss.

The document concludes that more research is needed to fully understand the causes of PCOS.

Genetic differences may affect COVID-19 deaths; anti-androgens could be potential treatment.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

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

PCOS has a strong genetic basis, but more research is needed to fully understand it.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.