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Implanted special stem cells from hair follicles helped heal wounds faster and with less scarring in mice.

Increasing type 17 collagen reduces aging signs in skin cells caused by UV light.

RCS-01 cell therapy is safe and improves skin gene expression.

Foxc1 and COL17A1 are crucial for maintaining healthy hair follicles and preventing hair loss.

Mice without collagen VI have slower hair growth normally but faster regrowth after injury.

Centipeda minima and brevilin A protect skin cells from damage and aging.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

A specific gene mutation causes severe skin and nail issues and hair loss.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Two new gene mutations cause a rare hair disorder.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A new mouse mutation causes skin and hair defects due to a gene change.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A new gene mutation is linked to monilethrix in the studied family.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Mutations in the hHb6 gene cause the hair disorder monilethrix.