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New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

AR polyglycine repeat doesn't cause baldness.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

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 certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Aromatase gene variation may increase female hair loss risk.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

DHT, a testosterone byproduct, causes male pattern baldness.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Parthenolide promotes hair growth in mice and may influence pathways related to male pattern baldness.

Men with Kennedy disease have less chance of hair loss.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Experts agree that PCOS affects women's health in complex ways, but more research is needed to understand and treat it effectively.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

PDGFA/AKT signaling is important for the growth and maintenance of certain skin fat cells.

The document concludes that accurate diagnosis of different types of hair loss requires careful examination of hair and scalp tissue, considering both clinical and microscopic features.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.