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

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

A new gene mutation causes a rare type of hair loss.

A new gene mutation causes insulin resistance in a girl and her mother.

A genetic marker linked to a type of hair loss was found in most patients studied.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

The vector successfully directed specific gene expression in hair follicles.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

A gene mutation causes monilethrix in a Chinese family.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

NFIC helps rat dental cells grow and turn into bone-like cells.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A new gene mutation is linked to monilethrix in the studied family.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Mice with more Flightless I protein grew back their claws better after amputation.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

New genetic mutations linked to rare skin disorders were found in three newborns.

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

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

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

The hr gene is linked to hair loss in Valle del Belice sheep.

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

A gene mutation in mice causes skin defects and early death.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.