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

The research found that a protein called PPARg is important for the formation and healing of sebaceous glands, which can regenerate independently from hair follicles.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

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

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Studying rare genetic disorders can help us understand and treat common diseases better.

Keratin proteins are crucial for hair structure and strength.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Mast cells likely promote skin scarring and fibrosis, but their exact role is still unclear.

Notch signaling disruptions can cause various skin diseases.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Estrogens and progesterone are key in regulating melasma pigmentation.

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.

Sirolimus and propranolol may reduce abnormal cell growth and improve lymphatic malformations in children.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.