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Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

New models predict male pattern baldness better than old ones but still need improvement.

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

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Certain genes may influence hair loss differently in men and women.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Men can have genetic risks for PCOS-related traits like obesity and diabetes.

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

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Experts discussed hair care, genetic hair defects, hair loss treatments, nail surgery, lupus treatments, skin infections, and cosmetic allergies.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

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

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.