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The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

The symposium highlighted the importance of understanding disease mechanisms for targeted dermatology treatments.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Recent selection on immune response genes was identified across seven ethnicities.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

No clear link between androgen receptor variation and hair loss, but more research needed.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Some wound-healing cells can turn into fat cells around new hair growth in mice.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Lgr5 is a marker for active, self-renewing stem cells in the intestine and skin, important for tissue maintenance.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

Women with telogen effluvium have lower levels of iron, folate, and vitamin B12.

Researchers found a new mutation causing total hair loss from birth.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

FPHL causes hair loss in women due to genetics and hormones; minoxidil and anti-androgens are treatments, and early intervention is advised.