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Neurosteroids like neuro-estrogen and neuro-androgen are crucial for brain function and can improve cognition and protect against aging-related decline.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

p120-catenin helps control skin inflammation by regulating cadherin levels.

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

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

CCC1 is essential for ion balance and proper plant cell function.

Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

Trps1 is essential for proper hair follicle development.

Human hair follicles produce and respond to erythropoietin, helping protect against stress.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

Hair follicle development involves specific cells and genes, crucial for understanding severe skin diseases like harlequin ichthyosis.

2-Hydroxy-1,4-naphthoquinone is a strong 5α-reductase inhibitor.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Microneedle technology is beneficial for drug delivery and could make vaccinations cheaper and more accessible.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

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

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.