NER in mammalian cells
A disease in humans known as Xeroderma Pigmentosum XP
is a rare inherited disease of humans which, among other
things, predisposes the patient to
 pigmented lesions on areas of the skin exposed to the sun
and
 an elevated incidence of skin cancer.
It turns out that XP can be caused by mutations in any one of
several genes - all of which have roles to play in NER.
James Cleaver went around and collected cells from hundreds
of these patients.  He then figured out that the disease was
made up of eight genes named XP-A through XP-G plus one
called XP-V for variant.