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The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

The glucocorticoid receptor helps protect skin from tumors and other issues.

RCS-01 therapy is safe and may improve skin structure by affecting gene expression.

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

ERULUS is crucial for root hair growth by controlling calcium levels.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

CRISPR-Cas9 can successfully edit genes in large mammals like Cashmere goats.

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

B-Raf and C-Raf are essential for maintaining melanocyte stem cells to prevent hair graying.

Activating cannabinoid receptor 1 may help manage psoriasis by reducing certain keratins.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Researchers found a non-functional sheep keratin gene due to mutations.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

Toll-like receptor 3 helps repair the skin barrier after UV damage.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

Neutrophils are key in causing chronic itch in atopic dermatitis, and blocking CXCR3 could reduce this itch.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Removing SIX1 in fat cells reduces skin fibrosis.

CRISPR-Cas9 successfully edited genes in Cashmere goats, affecting hair growth.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

Neutrophils are important for causing chronic itch in atopic dermatitis, and blocking the CXCR3 receptor may reduce this itch.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

The Arabidopsis rhd2 mutant is more sensitive to drought because of changes in cell membrane proteins and cell structure.