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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

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

ZDHHC17 methylation may help treat or identify facial skin aging.

Two sisters had a rare hair condition without other usual symptoms.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

The mTOR signaling pathway might play a role in radiation dermatitis, but more research is needed.

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

A gene mutation causes monilethrix in a Chinese family.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

Chemical treatments and UV radiation severely damage the lipid layer on hair.

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

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

SQSTM1 gene issues may increase the risk of alopecia areata.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The Gsdma3 gene is essential for normal hair development in mice.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

The role of γδT-cells in causing alopecia areata remains unclear.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.