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SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Whiskers can form without sensory nerves or Foxd1, thanks to Meis2 in mesenchymal cells.

The Yorkshire terrier has a genetic hair loss condition not improved by treatment.

Hair breaks differently when wet or dry and is affected by its condition and treatments like perms and bleaching.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

A mutation in the KRT74 gene causes tightly curled hair.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Trichodaganomania involves biting one's hair and needs combined psychological and medical treatment.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The conclusion is that self-concept, shame, and emotion regulation are key factors in hoarding disorder, body dysmorphic disorder, and trichotillomania, and should be targeted in treatment and research.

Tissue stiffness affects hair follicle regeneration, and Twist1 is a key regulator.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Telogen effluvium is a condition that causes temporary hair loss due to stress or shock to the body.

Hair proteins have weak spots in their α-helical segments.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

Healthy hair is crucial to avoid dryness, weakness, and breakage.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A gene deletion causes the "hairless" trait in Iffa Credo rats.