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Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

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

SIPHL1 from tomato enhances plants' response to low phosphate levels.

TSPO might help treat anxiety and depression.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Scientists identified a group of human skin cells with high growth and regeneration potential.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Recent selection on immune response genes was identified across seven ethnicities.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

UHP-sCESr is as effective as HESr for treating BPH symptoms.

The HCR gene contributes to psoriasis risk.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Heat shock protein 27 is more present in the active growth phase of human scalp hair follicles.

The new method is 1000 times more sensitive for measuring hair growth.

Substance P may contribute to hair loss by increasing oxidative stress and mitochondrial activity in hair follicles.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

New genetic variants linked to albinism were found in Pakistani families.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A new method helps find proteins in hair to identify fetal growth issues.

Hantavirus survivors often face long-term health issues, needing ongoing care.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Understanding and managing side effects of hedgehog pathway inhibitors can improve treatment for advanced basal cell carcinoma.