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HDAC inhibitors help brain cells grow and improve brain function.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Mouse hair follicle stem cells have a flexible chromatin state that supports skin health and hair growth.

The hepatitis B vaccine did not cause hair loss in the tested mice.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

ILC1-like cells can cause alopecia areata by themselves.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

A hepatitis B patient lost hair in patches after starting and stopping a treatment with pegylated interferon alpha2a.

ZO-1 helps hair follicle stem cells renew better by changing their structure.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Hominis Placenta helps hair grow back by increasing cell growth and a specific growth factor.