-
Xeroderma pigmentosum (XP) is a
genetic disorder in
which there is a
decreased ability to
repair DNA
damage such as that
caused by
ultraviolet (UV) light...
- XPB (xeroderma
pigmentosum type B) is an ATP-dependent DNA
helicase in
humans that is a part of the
TFIIH transcription factor complex. The 3D-structure...
-
Xeroderma Xeroderma pigmentosum Xeroderma pigmentosum, type 1
Xeroderma pigmentosum, type 2
Xeroderma pigmentosum, type 3
Xeroderma pigmentosum, type 5 Xeroderma...
- (RTS), ****ayne
syndrome (CS),
xeroderma pigmentosum (XP),
trichothiodystrophy (TTD),
combined xeroderma pigmentosum-****ayne
syndrome (XP-CS), restrictive...
- by lack of or
malfunctioning of DNA
ligase is as follows.
Xeroderma pigmentosum,
which is
commonly known as XP, is an
inherited condition characterized...
- that
result from in-born
genetic mutations of NER proteins.
Xeroderma pigmentosum and ****ayne's
syndrome are two
examples of NER ****ociated diseases....
- (Pigmented
layer labeled at
bottom right.)
Details Identifiers Latin stratum pigmentosum retinae, pars
pigmentosa retinae MeSH D055213 TA98 A15.2.04.008 TA2 6782...
-
result in
three different disorders: the cancer-prone
syndrome xeroderma pigmentosum complementation group D,
photosensitive trichothiodystrophy, and ****ayne...
-
mutant individuals often show the
severe clinical symptoms of
xeroderma pigmentosum, a
condition involving extreme sensitivity to
sunlight and a high incidence...
-
amino acid
linking the N- and I-regions are not conserved.
Xeroderma pigmentosum (XP) is a
human autosomal recessive disease,
characterised by a high...
