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HHV-6 reactivation may be linked to psychiatric disorders and can improve with antiviral treatment.

Researchers created an efficient method to extract DNA from marmoset hair, reducing blood chimerism.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

Careful monitoring is crucial to prevent JC virus reactivation in lupus patients treated with rituximab.

Dog skin with hair loss, when transplanted to mice, regrew hair, suggesting the hair loss cause is likely body-wide, not skin-specific.

MEG3-miRNAs help control wool traits in young Tan sheep by regulating immune responses, but their decline with age leads to wool changes.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Some families have a genetic condition where they are born with irregular scalp defects.

Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

The naked mutation in mice causes hair loss and helps identify keratin genes.

A new DSG4 gene mutation causes hair defects in a young girl.

Experienced professionals can fix bad scalp micropigmentation with good results.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Certain factors can trigger hormonal imbalances and cyst formation, leading to Polycystic Ovarian Syndrome (PCOS).

Dermal EZH2 controls skin cell development and hair growth in mice.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Mixed Connective Tissue Disease can develop from overlapping symptoms of several autoimmune diseases, making diagnosis complex.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

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

A 14-year-old girl's black hair showed unique color changes, suggesting early greying.

Targeting specific molecular pathways may improve treatments for chemoresistant cancers.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

Steroid injections improved symptoms and hair regrowth in a woman with a reaction to permanent makeup.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A specific gene mutation causes Olmsted syndrome.

CD146 + mesenchymal stem cells are more effective for treating premature ovarian failure.