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The interdigital gland of Vembur sheep shows sex-based differences in size and chemical makeup, possibly affecting communication and disease protection.

A gene mutation in Lama3 is linked to a common type of hair loss.

Smilax aristolochiifolia is declining in Puebla, Mexico, needing conservation efforts.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Four new FGF5 gene variants cause long hair in dogs.

Olive oil helps Malassezia globosa overgrow, worsening atopic dermatitis in mice.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

The spiny mouse can fully regenerate skin after burns, unlike the lab mouse.

Early diagnosis and treatment can effectively manage mite infestations in goats.

The study showed that brown planaria can be used to cheaply test if local plants can stop cell growth.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Stress is likely causing hair loss in Formosan macaques.

Enlarged sweat gland ducts may indicate scarring hair loss.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Researchers found genes linked to hair loss in male giant pandas.

Nevus comedonicus can appear later in life and affect both eyelids.

Trichoblastomas in rabbits are linked to uncontrolled embryonic hair growth and have distinct histological features.

A new gene causes hairlessness and skin cysts in rats.

Hairless mice lose hair by 3-4 weeks, develop thicker, folded skin, and show pigmentation differences.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

Pseudopelade can affect both the scalp and beard, causing hair loss.

Alopecia mucinosa is a challenging condition with unclear diagnosis and treatment.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

The southern elephant seal's skin layer helps waterproof the skin by being tightly connected to hair shafts.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

Ultrasonography improves pilomatricoma diagnosis accuracy.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.