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Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

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

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Farudodstat may help prevent hair loss in alopecia areata by stopping immune attacks on hair follicles.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

CDH3-related disease causes worsening eye and hair issues.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Somatic BHD mutations are rare in Japanese renal tumors.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Farudodstat may help treat alopecia areata by protecting hair follicles.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

ICAM-1 helps regulate hair growth cycles and skin remodeling.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

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

Farudodstat may effectively treat alopecia areata without harmful side effects.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Farudodstat may effectively treat alopecia areata without harming hair follicles.

The Hair Cell Analysis Toolbox automates and improves the analysis of cochlear hair cells using machine learning.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.