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Glutathione helps Arabidopsis roots adapt to low phosphate by regulating a specific growth pathway.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Daughters of women with PCOS generally experience normal puberty but may have more body hair and different body fat distribution.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Finasteride use may lead to less alcohol consumption in men with lasting sexual side effects.

ESR2 gene variations may be linked to female pattern hair loss.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.

Stump-tailed macaque best for researching hair loss causes and treatments.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

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

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

Insulin resistance is linked to high male hormone levels in women, often seen in those with PCOS.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Ozone therapy might improve cancer treatment and reduce its side effects.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The environment around melanocyte stem cells is key for hair regeneration and color, with certain injuries affecting hair color and potential treatments for pigmentation disorders.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Finasteride can cause sexual problems and depression in young men.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

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

AR gene not major factor in female hair loss; different from male hair loss.