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Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

T cells with memory features grow in number and gather around hair follicles when there are not enough immune cells.

MPA increases cancer spread by boosting Eph A2 activity.

An intact skin barrier is crucial to prevent infection in cases of tether-induced tenosynovitis.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

Tenascin is present in normal skin and certain skin tumors but not in sebaceous glands or their tumors.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Nestin helps identify certain melanoma cells in nodular melanoma.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Activated ras can protect kidney cells from a certain substance that causes cell death.

Robertsonian translocation can cause recurrent miscarriages.

An 8-year-old boy with hair-pulling disorder had a bald patch that was confirmed not to be a fungal infection and was treated with therapy.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Temozolomide can cause severe bone marrow suppression, leading to life-threatening complications.

The nodule on the woman's back was a benign hair follicle tumor, not cancer, but needed removal.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Some drugs for inflammation may cause psoriasis-like hair loss.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

TQC shows promise for better hair regrowth in treating hair loss.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.