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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Phospholipase C-δ1 is crucial for normal hair development.

Activating β-catenin in certain skin cells speeds up hair growth in mice.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

A peptide in shampoo can promote hair growth and improve hair condition.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

A DNA aptamer helps promote hair growth by enhancing a key cell growth signal in hair follicle cells.

DGAT1 enzyme is crucial for healthy skin and hair by regulating retinoid levels.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

A new genetic mutation was found causing hair and eye issues in a boy.

Activating β-catenin can turn skin cells into hair follicles.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

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

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

Cantú syndrome is caused by mutations in the ABCC9 gene.

Mutations in specific genes cause different types of ectodermal dysplasias.

FOXN1 duplication can cause excessive hair growth.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

Increased ODC expression makes normally tumor-resistant mice more prone to tumor development.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

HDAC1 is crucial for skin development and preventing tumors.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.