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The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Two gene areas linked to male pattern baldness found, more research needed.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Alfacalcidiol and metformin together lowered testosterone in women with PCOS, but did not significantly improve acne, hair growth, or pregnancy rates.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

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

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

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

Placental growth factor may help treat hair loss.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

No link found between new male baldness genes and female hair loss.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

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

Early hair loss links to metabolic issues in young Indian men.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

No link found between aromatase gene and female hair loss.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

MC4R gene variants not linked to female hair loss.