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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Actin filaments help stabilize and reshape cell membranes.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

DNA microarrays help study skin diseases and biology, leading to advancements in understanding and treatment.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.

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

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

TSC2 is crucial for proper hair follicle development and patterning.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Targeting the p300/AR axis may help treat polycystic ovary syndrome.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

SWI/SNF complexes are crucial for wound healing but not for hair growth.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

miR-140-y helps control feather growth in geese by affecting the Wnt signaling pathway.

Certain gene variations increase the risk of alopecia areata in Koreans.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.