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Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

There are two ways to start hair growth: one needs Stat3 and the other does not, but both need PI3K activation.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

FoxN1 overexpression in young mice harms immune cell and skin development.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

The enzyme sEH is important for hair growth and its inhibition could help treat hair loss.

Jarjeer has potential health benefits and may aid hair growth, but effects on humans are uncertain.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Raccoon dogs in Schleswig-Holstein, Germany, were found with sarcoptic mange, showing severe skin issues and potential for spreading the disease.

Spironolactone can cause side effects like high potassium levels and breast enlargement, and patients need careful monitoring.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Certain fungi and bacteria help orchid seeds germinate and plants grow better.

CCC1 is essential for ion balance and proper plant cell function.

CCC1 is essential for pH balance and normal cell function in plants.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

The supplement highlighted advancements and challenges in plastic and reconstructive surgery, including the impact of smoking, chemotherapy, and new treatments like Tafluprost for hair loss.

A gene mutation causes woolly hair in a Syrian patient.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

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

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

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

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

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.