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The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

HXBSM boosts blood vessel growth and hair growth in mice.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

LHX2 is crucial for development, tissue repair, and preventing diseases.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A genetic marker linked to a type of hair loss was found in most patients studied.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

HAP stem cells can repair nerves and spinal cords by becoming Schwann cells.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

hsa_circ_0001079 may help diagnose and treat hair loss.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Mutations in hKAP1 genes may cause hereditary hair disorders.

LHX2, with other markers, can identify hair placodes in rats.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Increasing TSPO in the brain reduces anxiety and depression.