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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Ectoin helps prevent cortisone-induced skin problems and supports skin health.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

Obstructive sleep apnea can be hereditary and linked to a genetic mutation in the COL1A2 gene.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

The study found specific skin cells and genes that may affect the quality of cashmere in Liaoning Cashmere Goats.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

CLE14 peptide promotes root hair growth in Arabidopsis.

BLMP-1 is important for regular molting and gene expression cycles in worms.

Twelve key genes may improve cashmere production by influencing hair follicle cycles.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

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

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

c-Kit is important for heart regeneration and cancer development.

MYC protooncogenes may be important for hair growth, but more research is needed.

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

Defects in certain proteins cause major heart abnormalities during early development.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

Skin cysts might help advance stem cell treatments to repair skin.