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Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

Longer CAG repeats in gene linked to more severe hair loss in females.

A male with aromatase deficiency improved bone health with estradiol treatment.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

No link found between specific genes and female pattern hair loss.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

CAG repeat length in the AR gene is not linked to PCOS risk in Iranian women.

Certain gene variations may increase the risk of hair loss in Egyptians.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

miR-200c-3p could help diagnose and treat alopecia areata.

TAp63 and NRF2 work together to manage oxidative stress, preventing premature aging and aiding skin functions.

ZDHHC17 methylation may help treat or identify facial skin aging.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

COL17A1 is crucial for preventing hair graying and loss by supporting hair and pigment stem cells.

Genetic variations may affect how well finasteride works for BPH patients.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.