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Immunofluorescence tomography is a cost-effective method for creating detailed 3-D images of tissues.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Parathyroid hormone-related protein helps control hair growth phases in mice.

A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Hair transplantation successfully treated hair loss in a patient with Trichorhinophalangeal syndrome.

Women with PCOS have higher body fat and skinfold thickness, especially in the H-O-POM phenotype.

Normal hair density and diameter ratios were established to help diagnose adult hair loss.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Oligomenorrhea is the strongest predictor of PCOS severity.

Marsupial hair structure and keratin distribution are similar to placental mammals.

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

A girl had rickets due to a gene mutation affecting vitamin D response.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Mitochondria change shape to meet energy needs during cell movement.

PHAs are promising biodegradable materials for medical and dental uses.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

Thorough hair examination is crucial for accurate diagnosis and treatment.

An 8-year-old boy's early puberty was caused by a rare hormone-secreting brain tumor, which was successfully treated with surgery.

The document's conclusion cannot be summarized as it is not provided in a language I can understand.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

Modified steroidal inhibitors showed promise in treating hormone-dependent cancers.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Best results found using acetonitrile, water, and trifluoroacetic acid or methanol mixture.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

A specific gene mutation causes congenital hair loss.

Researchers made new compounds that could potentially be developed into anticancer drugs.