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TGM3 is important for skin and hair structure and may help diagnose cancer.

A rare benign skin nodule was found on the buttock, a unique location for this condition.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Tufted folliculitis is common in patients with folliculitis decalvans.

Long-term use of minoxidil may cause hair follicles to transform into noticeable terminal hairs, leading to trichostasis spinulosa.

Engineered skin can grow chimeric hair follicles only with mouse dermal papilla cells.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

EGFR inhibitors can cause unusual localized hair growth.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Nested PCR can reliably identify fungal infections when traditional methods fail.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

Low-cost dermoscopes can effectively diagnose early female pattern hair loss.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

A method was developed to grow millions of hair cells from a single hair for research and storage.

Trichotillomania is an obsessive-compulsive disorder causing hair pulling, needing complex treatment to prevent serious issues.

Trichotillomania, a disorder where people compulsively pull out their own hair, often starts around age 12, is more common in adult females, and can be treated with behavior therapy and medication.

Trichotillomania is a chronic hair-pulling disorder, more common in females, treated with therapy and sometimes medication.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A gene mutation in mice causes permanent hair loss and skin issues.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

A deep learning model accurately predicts male hair loss types using scalp images.

A young girl developed unusually long eyelashes with a hair loss condition without other health issues or medication causes.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

TG5 helps maintain hair follicle health, while TG3 aids in hair shaft development.