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Mouse hair follicle cells briefly grow during the early hair growth phase, showing that these cells are important for starting the hair cycle.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

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

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Sebaceous gland organoids could improve skin regeneration and treatment.

Collagenous gastritis is a rare condition causing chronic diarrhea and weight loss, often misdiagnosed due to nonspecific symptoms.

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

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Retinoic acid causes gland formation instead of hair in mouse skin by altering epidermal and dermal interactions.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

The research found that specific stem cells maintain skin gland openings and that disrupting their activity can cause blockages or early cancer signs, indicating a need for targeted treatments.

A woman with dermatomyositis improved after treatment for neck panniculitis, suggesting similar treatment for related conditions.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

The study found stem cells in minor salivary glands that can differentiate and are involved in tumor formation when exposed to tobacco.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Muscle around hair follicles controls hair loss by releasing a signal that causes cell death.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

A man had a black pore on his cheek, which was removed and found to be a hair follicle tumor.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Mesenchymal stiffness affects sweat gland cell development.

A rare skin growth in a baby was successfully removed without coming back.

Keratoacanthomas on lips may originate differently than those on skin.

A man with skin and hair symptoms improved partially with specific treatment.

An elderly man with skin amyloidosis and abnormal blood proteins was monitored without finding widespread disease after 18 months.

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