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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

Proper hair care can prevent and stop hair breakage in people with acquired trichorrhexis nodosa.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

Weak cell junctions disrupt hair follicle stem cell rest.

Transglutaminase-3 is often reduced in esophageal cancer.

TQC shows promise for better hair regrowth in treating hair loss.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Cetuximab can cause eyelash growth, which is rare but manageable.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

A rare scalp tumor was removed from a 49-year-old woman, with a good outlook if benign but needing careful monitoring if malignant.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

TRH stimulates human hair growth and extends the hair growth phase.

Egfl6 is not needed for zebrafish face development.

A baby boy's toe was saved from damage caused by hair strangulation by quick surgical treatment.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Monilethrix is linked to a gene cluster on chromosome 12.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.