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Shrinking of oil glands in the skin is a key sign of hair loss linked to TNF inhibitor drugs and may improve if the treatment is stopped.

PHGDH promotes cancer growth by aiding cell proliferation and tumor progression.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

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A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Sox13 is a useful marker for early hair follicle development but not essential for hair growth.

Choosing the right recall period for patient feedback is important for accurate data and depends on the disease, symptom changes, and patient impact.

Ancient South American mummies' hair shows high sulfur, calcium, and potassium levels.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Certain inhibitors applied to the skin can promote hair growth by maintaining a key hair growth signal.

New mouse models help study melanocytic cells for melanoma research.

Hair loss (telogen effluvium) happens before male pattern baldness.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Disrupted stem cell signals in hairpoor mice cause hair loss.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

PRP-based treatments can increase hair density, but results vary among individuals.

A specific enzyme is crucial for the bean plant's relationship with certain beneficial soil bacteria and fungi.

The study found that minor protein differences between curved and straight Japanese hair are unlikely to significantly affect hair structure.

The dermal sheath's contraction is crucial for hair follicle regression and stem cell relocation.

A reliable method was developed to measure Tamsulosin and Finasteride in tablets accurately.

Human hair follicles may provide a noninvasive way to diagnose diseases and have potential in regenerative medicine.

Nestin is found in hair follicle progenitor cells, linking them to neural stem cells.

Familial sexual precocity in girls may be more common than previously thought.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Frontal fibrosing alopecia can mimic traction alopecia but has distinct features like facial papules and eyebrow thinning.

The P&P Hairline Laser is a new, hands-free device that improves hairline symmetry in hair restoration surgery and can create a symmetrical hairline in less than a minute.