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α-Phellandrene may help prevent hair loss by increasing growth factors and cell growth in hair cells through a specific signaling pathway.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

HPV genes and estradiol increase a cancer-related signaling pathway, which may be targeted for cervical cancer treatment.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Mutations in the KRT16 gene can cause skin and nail disorders.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

MCSP may help identify and regulate skin stem cells, affecting hair growth and regeneration.

Different types of cells in the eye express specific keratins at various stages of development.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

MEF2C is crucial for normal hair cycle progression.

EZH2 is essential for hair growth and skin cell development.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

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

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

Mouse and human skin development share similar fibroblast timelines.

A baby girl had two brain-related growths removed and is developing normally.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

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

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

Dermal papilla cell vesicles can boost hair growth genes in fat stem cells.

A truncated protein linked to breast cancer may change cell adhesion.

FoxN1 overexpression in young mice harms immune cell and skin development.