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Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

A new mutation in the HR gene causes hair loss in a specific family.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

HLA can be linked to autoimmune hepatitis.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

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

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

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

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

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

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Hhip-Cre effectively targets dermal papilla cells for gene manipulation in hair biology.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

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

MOF controls skin development by regulating genes for mitochondria and cilia.

Vitamin D receptor and hairless protein are essential for hair growth.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

H2AK119ub helps keep hair follicle stem cells in a resting state, preventing early aging.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

A gene mutation causes monilethrix in a Chinese family.