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A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

Cyclosporine effectively treated a woman's stubborn skin condition.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

TGF-alpha affects skin thickness, hair growth, and may contribute to psoriasis and papilloma formation.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Severe CCCA may be biologically and clinically different from milder forms.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

A new method can almost perfectly distinguish adenomyosis from similar conditions using blood tests.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

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.