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Xeroderma,
xerosis or
xerosis cutis, or
simply dry skin, is a skin
condition characterized by
excessively dry skin. The term
derives from Gr**** ξηρός...
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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...
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syndrome (RTS), ****ayne
syndrome (CS),
xeroderma pigmentosum (XP),
trichothiodystrophy (TTD),
combined xeroderma pigmentosum-****ayne
syndrome (XP-CS)...
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Vitamin A
deficiency (VAD) or
hypovitaminosis A is a lack of
vitamin A in
blood and tissues. It is
common in
poorer countries,
especially among children...
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hereditary Xeroderma Xeroderma pigmentosum Xeroderma pigmentosum, type 1
Xeroderma pigmentosum, type 2
Xeroderma pigmentosum, type 3
Xeroderma pigmentosum...
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common adverse effects are dry lips (cheilitis), dry and
fragile skin (
xeroderma), dry eyes and an
increased susceptibility to sunburn.
Uncommon and rare...
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diseases caused by lack of or
malfunctioning of DNA
ligase is as follows.
Xeroderma pigmentosum,
which is
commonly known as XP, is an
inherited condition...
- in XPG. The
amino acid
linking the N- and I-regions are not conserved.
Xeroderma pigmentosum (XP) is a
human autosomal recessive disease, characterised...
-
diseases that
result from in-born
genetic mutations of NER proteins.
Xeroderma pigmentosum and ****ayne's
syndrome are two
examples of NER ****ociated...
