Search

everythinglearnresearchcommunity

for

Search:↓

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Betamethasone dipropionate reduced skin thickness, fish oil increased it, and combined treatment had no significant effect.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

Hair growth and development are controlled by specific signaling pathways.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Weight loss and metformin don't significantly change vaspin levels in women with PCOS.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Light microscopy is useful for diagnosing different hair disorders.

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

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Researchers found a gene mutation responsible for a rare hair loss condition.

The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

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

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.