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Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Desmocollin 1 is essential for strong skin and proper skin function.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

A new method quickly and efficiently isolates hair follicle stem cells from adult mice, promoting hair growth.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

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

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Epidermis and dermis cells together can regenerate hair follicles.

Engineered exosomes with EGF and FGF improved hair growth in mice with hair loss.

Activin A and Follistatin affect how mouse hair follicles grow.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

The K5 promoter controls gene expression in skin cells, with specific DNA segments crucial for targeting and regulation.

A specific molecular switch, driven by MAPK/ERK signaling, helps spiny mice heal wounds by regenerating skin instead of forming scars.

The p53 protein helps control hair follicle shrinking by promoting cell death in mice.

Jagged1 and Epidermal Growth Factor together significantly increased hair growth in mice with androgen-suppressed hair.

Transplanted whisker follicles caused long hair growth on the spinal cords of mice.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The HCR gene contributes to psoriasis risk.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

FGF and EGF are crucial for hair follicle development and growth.