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Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Patients with acute and subacute skin lupus respond faster to belimumab than those with chronic skin lupus.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A special hydrogel helps heal skin without scars and regrows hair.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Low Vitamin D is common in people with Alopecia Areata, but its impact on the condition needs more research.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Hair follicles produce IL-7, which is essential for certain skin lymphoma cells to survive.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

Beard hair follicles have more androgen receptors than non-balding scalp hair follicles.

Low-oxygen conditions and ECM degradation products increase the healing abilities of perivascular stem cells.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Measuring the distance from the anus to the clitoris may moderately help diagnose polycystic ovary syndrome, especially in certain cases.

Henna dye improves hair cuticle and thickness but effects vary by hair type and health.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Foxn1 is important for fat development, metabolism, and wound healing in skin.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

A protein called MPZL3 in mitochondria slows down hair growth and could be a target for treating hair growth disorders.

Polycystic Ovary Syndrome (PCOS) symptoms vary globally, with bloating, high cholesterol, and glucose levels being common; the current diagnostic criteria may need refining.

Trichoscopy helps detect early complications in hair transplants and ensures quality in the procedure.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

FGF13 gene changes cause excessive hair growth in a rare condition.

Magnesium oxide-infused membranes help heal wounds faster by reducing inflammation and promoting skin and hair follicle growth.

The study created a tool that mimics natural cell signals, which increased cell growth and could help with hair regeneration research.