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Certain immune cells in the skin release a protein that stops hair growth by keeping hair stem cells inactive.

A 308 nm excimer laser successfully treated a boy with a rare skin condition after about a year of weekly sessions.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

ME1 and PPAR signaling may influence hair loss in androgenetic alopecia.

Defective T cell metabolism can cause early skin aging and poor hair follicle stem cell function.

Hypothyroidism may worsen metabolic problems like insulin resistance and obesity in women with PCOS.

Replacing defective mesenchymal cells with normal ones fixes thymic growth issues in 22q11.2DS mouse models.

Tetrathiomolybdate reduces hair growth marker in skin cells by boosting harmful oxygen molecules, but effects can be reversed.

miR-486 may help prevent hair loss in alopecia areata.

Hydrophobic modifications make human hair less affected by water.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A new gene mutation causes a rare type of hair loss.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Methotrexate is not proven to maintain remission in ulcerative colitis.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

DM and AA may share a common cause.

Miniaturized hair follicles in androgenetic alopecia show abnormal mitochondrial activity and damage.

PCOS women have more severe metabolic issues and higher androgen levels than hyperandrogenic women without PCOS.

Pilomatricomas don't follow the usual hair follicle cell differentiation process.

Vitamin B12 deficiency can cause skin and hair color changes, which can be reversed with treatment.

The research found enzymes in Stephania epigaea that help make cepharanthine.

Artemis dysfunction might cause hair loss through telomere shortening.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

New method makes important drug ingredients more easily without needing extra purification steps.

A new mutation in mice causes crooked whiskers and messy hair.

A specific mutation in PA-PLA1α causes abnormal hair growth.

miRNAs are crucial for hair growth and skin health.

The study found that p63 needs signals from morphogens to help skin cells differentiate properly.