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HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

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

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

HLA can be linked to autoimmune hepatitis.

HLD10 can include increased body hair and Mongolian spots.

LHX2 is crucial for development, tissue repair, and preventing diseases.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Mutations in the LIPH gene cause woolly hair in a child.

hHbl gene is active in hair shaft cells and some pilomatricomas.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Lhx2 helps retinal cells respond to signals for eye development.

Human hair has a protective lipid layer that can be damaged by moisture and treatments, affecting hair growth and health.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Lipase H is important for hair follicle function and shaping hair fibers.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

HAPLN1 can promote hair growth and may help treat hair loss.

LIPH mutations cause woolly hair in some Chinese people.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

LHX2, with other markers, can identify hair placodes in rats.

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

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.