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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

CRISPR/Cas systems show promise for cancer treatment by targeting miRNAs, but delivery and specificity challenges remain.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

Keratin 15 affects cell behavior and characteristics in skin cells.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Gene expression affects fur development in rex rabbits.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Blocking Rab27a slows hair growth, while blocking Rab27b encourages it.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

The new particle system could be a promising treatment for diseases related to the 5-α reductase enzyme.

ceRNA networks offer potential treatments for skin aging and wound healing.

FOXN1 duplication can cause excessive hair growth.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.