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

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Genetic variations affecting skin structure play a key role in severe acne.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

Genetic discoveries are leading to new treatments for alopecia areata.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

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

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.

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.

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

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

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

Mitochondria may influence how cells respond to radiation, affecting nearby non-irradiated cells.

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

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

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

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

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

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

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

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.