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The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Overexpression of activin A in mice skin causes skin thickening, fibrosis, and improved wound healing.

Mice without certain skin proteins had abnormal skin and hair development.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

RT1640 treatment reverses gray hair and promotes hair growth in mice.

Excess androgens may cause PCOS, not just be a symptom.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Inflammation plays a key role in activating skin stem cells for hair growth and wound healing, but more research is needed to understand how it directs cell behavior.

Hair growth environment recreated with challenges; stem cells make successful skin organoids.

Hormonal therapies are safe and effective for treating adult women's acne.

Chicken feather gene mutation helps understand human hair disorders.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

PCOS is a complex disorder in women that can lead to various health risks and requires personalized treatment.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

Activin A and follistatin control when hair cells develop in mouse ears.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The new hair graft device is faster, more efficient, and reduces damage to hair follicles.

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

A group has developed therapies that show promise for treating cancer and various other conditions.

Nuclear hormone receptors play a significant role in skin wound healing and could lead to better treatment methods.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.