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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.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The 4C32 gene may help in mouse skin development and differentiation.

Different forms of the Vitamin D receptor can impact metabolic and hormone issues in Polycystic Ovary Syndrome.

The piRNA pathway genes are crucial in early development and may influence sex differentiation through hormone regulation.

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Methamphetamine affects gene expression in rat whisker follicles, with key genes linked to addiction.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Rat dermal papilla cells have unique genes crucial for hair growth.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

A rabbit gene important for hair development was identified and detailed.

Activin B can boost hair growth by promoting cell proliferation and cell cycle progression.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

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

Effective delivery of gene editors is crucial for safe and successful gene editing in healthcare and agriculture.

Different keratins have unique expression patterns in mouse skin cells.

These gene variations are not linked to alopecia areata in Egyptians.

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

VEGF-A is crucial for normal skin function and may be linked to psoriasis.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The Eda gene helps regulate the hair cycle in goats.

ATP-sensitive potassium channels are important for hair growth.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

The UHS promoter is specific to mouse hair follicles.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

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