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A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Targeting Sirt1 can reduce androgen levels and slow glioblastoma growth.

PFOS exposure disrupts hormone levels and enzyme activities in juvenile frogs, affecting males and females differently.

N-WASP is essential for healthy skin and preventing inflammation.

Serotonin helps wounds heal faster.

TAp63 and NRF2 work together to manage oxidative stress, preventing premature aging and aiding skin functions.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Dermal EZH2 controls skin cell growth and differentiation in mice.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Jag2 is essential for proper skin cell differentiation and organization.

Spiny mice have resilient, large mitochondria that help them regenerate tissue.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

The B2C promoter works in sheep cells but not in mouse embryos.

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

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

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.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Suppressing ODC activity reduces tumor growth in hair follicles.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.