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The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

PRP treatment can safely improve short-term vision in acute NAION patients.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Genetic defects and UV radiation cause skin damage and aging.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

FGF5 gene mutations cause long hair in domestic cats.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Disabling the FGF5 gene in sheep leads to longer wool.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

Many women with polycystic ovary syndrome have normal blood sugar, but some may have higher blood sugar levels or diabetes, especially if they are older, overweight, and have certain hormone levels.