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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The study suggests that a specific type of immune cell, memory-like NK cells, may increase during active hair loss in Alopecia areata.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Mutations in the DSG4 gene cause specific hair and scalp issues.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Targeting specific T cells may help treat alopecia areata.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

miR-200c-3p could help diagnose and treat alopecia areata.

Tph cells are linked to the severity of systemic lupus erythematosus.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

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

A man developed autoimmune issues after a transplant, improved with treatment, but died from leukemia relapse.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

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

No clear link between specific gene and hair loss in Mexican brothers.

The CD4 protein may play a role in the behavior of certain skin cells, affecting their growth, movement, and differentiation.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Male pattern baldness is likely caused by multiple genes, not just 5α-reductase genes.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

A man got six skin cancers within a year after a cell transplant for leukemia but was cancer-free 32 months later; skin checks are important post-transplant.

A mutation in the human hairless gene causes alopecia universalis.