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The study developed a 3D model that closely imitates remaining ovarian cancer after treatment and identified a potential drug targeting resistant cancer cells.

Overexpression of a specific receptor in mice skin causes skin thinning, early skin barrier formation, eye issues, and hair loss.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Kdm6b is crucial for skin cell differentiation.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

DKK proteins could help diagnose and treat various non-cancerous diseases.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Hair repigmentation can indicate malignancy and should be investigated.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

A man had a rare skin cancer that looked like a bald spot.

A substance called DKK-1 increases in balding areas and causes hair cells to die when exposed to DHT.

The donkey had a severe disease affecting multiple organs and was euthanized.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

A 70-year-old woman with a malignant adrenal tumor improved after surgery and radiotherapy.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Many women with melasma also have metabolic syndrome.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Specific mutations in a receptor cause facial abnormalities and hair loss.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Folliculotropic mycosis fungoides has a worse prognosis than other types, with survival rates varying significantly based on subtype and organ involvement.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.