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A dog in Germany was successfully treated for a rare bacterial infection without spreading it to humans.

Removing SIX1 in fat cells reduces skin fibrosis.

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

CD98hc's role in skin health decreases with age.

A rat had a cyst similar to a hair follicle structure.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Sensory neuron remodeling and Merkel-cell changes in the skin happen independently.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

A cat in Brazil was found with a severe skin condition linked to feline AIDS.

A fungal infection caused skin lesions in farmed mink kits, but they remained healthy.

A person with thyroid problems had rare, swollen, bald spots on their scalp caused by a condition usually found on the shins.

Malassezia-associated dermatitis can cause itching in cats with feline paraneoplastic alopecia.

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

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

A cat developed a skin lesion from a topical solution, which healed with minoxidil treatment.

The scraggly mutation causes hair loss and skin defects in mice.

Follicular mucinosis can be an early sign of aggressive mycosis fungoides.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Different melanocyte types in hair follicles either survive or die during the catagen phase.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

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