There are partial holes in at at one end. You insert a small amount of dyed DNA (etc) containing solution each. Apply an electrical potential across the gel. DNA gradually moves along. Smaller DNA fragments move faster. So, at a given time, you can coarsely measure fragment size of a given sample. Your absolute scale is given by "standards", aka "ladders" that have samples of multiple, known sizes.
The paper authors cheated (allegedly) by copy + pasting images of the gel. This is what was caught, so it implies they may have made up some or all results in this and other papers.
The problem are the vertical labels
In Figure 1e it says: "MT1+2", "MT2" and "MT1"
In Figure 3a it says: "5'-CR1", "CR2" and "3'-UTR"
In Figure 3b it says: "CR2", "CR3" and "CR4"