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Lack of sleep in mice leads to prostatitis by reducing certain hormones and activating an inflammatory pathway, which can be temporarily fixed with normal sleep.

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.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Sebum helps protect human skin from microbes.

Late dumping syndrome after fundoplication can be diagnosed with an oral glucose tolerance test and managed with diet changes.

A 31-year-old man has a chronic skin condition with red plaques, hair loss, and swollen lymph nodes.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Cells that move well may improve hair loss treatments by entering hair follicles.

Increasing TSPO in the brain reduces anxiety and depression.

Blocking Prostaglandin D₂ may help treat hair loss.

Lower doses of dexamethasone can safely reduce high DHEAS levels in women with androgenic disorders.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

The injectable hydrogel effectively speeds up chronic wound healing.

New technologies improve diagnosis and treatment of digestive disorders.

Dermatoscopy and videodermatoscopy are useful and reliable for tracking treatment progress in various skin conditions.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

People with Down's syndrome often have more skin problems due to a weak immune system.

The treatment led to significant hair regrowth in a lupus patient.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

Finasteride reduces certain behaviors caused by D1-like receptor agonists but not by D2-like receptor agonists in mice.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Dermatologic surgery has greatly improved with new techniques over the years.

Next-Generation Sequencing improves forensic analysis by providing detailed genetic information quickly.

Dihydrotestosterone can be made from dehydroepiandrosterone in skin cells without needing testosterone.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.