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A new DSG4 gene mutation causes hair defects in a young girl.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

K14 expression in young rats differs from adults.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

KRTAP28-1 gene can help breed sheep with finer wool.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

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.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Researchers found 15 new genetic links to skin traits in Japanese women.

Mutations in the P2RY5 gene cause hereditary woolly hair.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

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

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

A specific genetic deletion in goats affects cashmere yield and thickness.

Keratin 14 is uniquely found in a specific group of placental cells.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.