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New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

The review recommends hormone replacement therapy for women with premature ovarian insufficiency to manage symptoms and protect health, with specific approaches for different groups.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

AR polyglycine repeat doesn't cause baldness.

Apoptosis is crucial for healthy skin and treating skin diseases.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

SHBG may be a useful early indicator and treatment target for PCOS.

Researchers found 15 new genetic links to skin traits in Japanese women.

Male pattern hair loss caused by follicular miniaturization; early diagnosis and treatment can reduce psychological burden.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Skin stem cells maintain and repair the outer layer of skin, with some types being essential for healing wounds.

Female pattern hair loss is common, linked to polycystic ovarian syndrome, and treated with topical Minoxidil.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Vitamin D receptor is crucial for starting hair growth after birth.

Hair can regrow after certain stem cells are lost because other stem cells can take over their role.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Keratins are important for skin cell health and their problems can cause diseases.

Finasteride can reduce fertility in some men, but stopping it increases sperm count.

AMH helps estimate ovarian reserve but doesn't predict pregnancy chances; age is more important.

Cancer treatments often cause hair disorders, significantly affecting patients' quality of life, and better management methods are needed.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

The study suggests smoking is common in HS patients but its role is unclear, and more research is needed to understand HS causes.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.