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ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

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

Targeting the TNFRSF1B gene may help treat hair loss.

Inhibiting SFRP1 may help treat hair loss.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Actin filaments help stabilize and reshape cell membranes.

CD206+ macrophages are crucial for hair growth in alopecia areata treatment.

Malassezia restricta may be linked to intestinal diseases like Crohn's and ulcerative colitis.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

R-Spondin-1 is important for skin health and could help diagnose and treat various skin conditions.

Loss of Rap1 protein speeds up heart aging in mice.

Collagen XVII and CD151 affect cell movement, with CD151 inhibiting migration when bound to integrins.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

ARHGEF3 is essential for proper hair follicle development in mice.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

A specific type of immune cells, called CD301b-expressing macrophages, are crucial for skin repair processes.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.