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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

K6hf is a unique protein found only in a specific layer of hair follicles.

Some families have a genetic condition where they are born with irregular scalp defects.

The B2C promoter works in sheep cells but not in mouse embryos.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

SELP::KP improves hair strength, elasticity, and health, making it a promising hair cosmetic.

Researchers found genes in sheep that may affect hair growth and wool quality.

The new Mercedes flap variant effectively closed medium-sized scalp defects in a single operation with good cosmetic results and no complications.

Early diagnosis, genetic testing, and personalized care are essential for managing tuberous sclerosis.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

PLIN2 affects hair growth in cashmere goats, potentially improving cashmere quality.

Cutting and implanting hair follicles can create finer, more natural-looking hairlines, with about half of the implanted hairs growing back.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

SFRP2 and PTGDS may be key factors in female hair loss.

Thicker hair grows faster; hair loss patients have slower growth.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Removing Lrig1-positive stem cells in mice causes temporary loss of sebaceous glands.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

CTCF protein is essential for skin and hair follicle development in mice.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.