ఇచ్థియోసిస్ యొక్క తేలికపాటి రూపం చర్మం యొక్క అసాధారణ పొడి మరియు కరుకుదనం కలిగి ఉంటుంది,

Noun:

చర్మం కరుకుదనం, చర్మం, చర్మము శోధము,

xeroderma's Usage Examples:

He is credited with the description of xeroderma pigmentosum, a rare genetic disorder now known to be caused by defects in nucleotide excision repair (Ueber Xeroderma pigmentosum.

genes are absent, these mutations can lead to human syndromes, including xeroderma pigmentosum, Cockayne syndrome and Fanconi anemia.

The surface of the knuckles of a hand with xeroderma, showing skin cracking (generalized skin fissuring).

Xpa mutant individuals often show the severe clinical symptoms of xeroderma pigmentosum, a condition involving extreme sensitivity to sunlight and.

XPB (xeroderma pigmentosum type B) is an ATP-dependent DNA helicase in humans that is a part of the TFIIH transcription factor complex.

In humans, mutational defects in the ERCC5(XPG) gene can cause either the cancer-prone condition xeroderma pigmentosum (XP) alone, or in combination with the severe neurodevelopmental disorder Cockayne syndrome (CS) or the infantile lethal cerebro-oculo-facio-skeletal syndrome.

gene can result in three different disorders: the cancer-prone syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy.

Multiple investigations suggests that the xeroderma pigmentosum group A (XPA) and replication protein A (RPA), which are NER factors, are able to bind specifically as a complex to cross-linked triplex structures.

syndrome (RTS), Cockayne syndrome (CS), xeroderma pigmentosum (XP), trichothiodystrophy (TTD), combined xeroderma pigmentosum-Cockayne syndrome (XP-CS).

"Centrosome protein centrin 2/caltractin 1 is part of the xeroderma pigmentosum group C complex that initiates global genome nucleotide excision.

DeSanctis–Cacchione syndrome or Xeroderma pigmentosum is a Genetic disorder characterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring.

cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of.

also known as XPV, because loss of this gene results in the disease xeroderma pigmentosum.