| URN | urn:agi-Regulation:inout-urn:agi-llid:7507:out-urn:agi-meshdis:Xeroderma%20Pigmentosum::unknown |
|---|---|
| References | 7 |
| Connectivity | 2 |
| Effect | unknown |
| Original # of References | 7 |
| TextRef | info:pmid/2234061#abs:8 |
|---|---|
| PubYear | 1990 |
| MedlineTA | Nature |
| MedLine Reference | 2234061:7 |
| Sentence | These results indicate that a defective XPAC gene causes group A Xeroderma pigmentosum. |
| TextMods | 65: 'XP' -> 'Xeroderma pigmentosum' |
| TextRef | info:pmid/10699759#abs:5 |
|---|---|
| PubYear | 2000 |
| MedlineTA | J Dermatol Sci |
| Organ | Skin |
| MedLine Reference | 10699759:4 |
| Sentence | xeroderma pigmentosum involves seven genes of the nucleotide excision repair system (XPA through G). |
| TextMods | 0: 'XP ' -> 'xeroderma pigmentosum ' 50: 'NER ' -> 'nucleotide excision repair ' |
| TextRef | info:pmid/9439661#abs:3 |
|---|---|
| PubYear | 1997 |
| MedlineTA | Hum Genet |
| MedLine Reference | 9439661:2 |
| Sentence | Squamous cell carcinomata also develop as one of the complications of xeroderma pigmentosum, and one of the xeroderma pigmentosum genes (XPA) maps within the MSSE interval. |
| TextRef | info:pmid/9256505#body:30 |
|---|---|
| PubYear | 1997 |
| MedlineTA | Proc Natl Acad Sci U S A |
| Organ | Nerve |
| MedLine Reference | 9256505:1029 |
| Sentence | Xeroderma pigmentosum can be caused by mutations in any one of seven genes, XPA through XPG (1). |
| TextMods | 0: 'XP ' -> 'Xeroderma pigmentosum ' |
| TextRef | info:pmid/18285820#body:179 |
|---|---|
| PubYear | 2008 |
| MedlineTA | EMBO J |
| Organ | Eye |
| MedLine Reference | 18285820:1178 |
| Sentence | xeroderma pigmentosum is caused by mutations of the nucleotide excision repair gene XPA, XPB (ERCC3), XPC, XPD (ERCC2), XPE (DDB2), or XPF; XPG. |
| TextMods | 0: 'XP ' -> 'xeroderma pigmentosum ' 52: 'NER ' -> 'nucleotide excision repair ' |
| TextRef | info:pmid/10024877#body:82 |
|---|---|
| PubYear | 1999 |
| MedlineTA | Mol Cell |
| MedLine Reference | 10024877:1081 |
| Sentence | In contrast, nucleotide excision repair defects generally are nonlethal, and mutations in any of the 7 key genes XPA to XPG can be the cause of the inherited cancer-prone disease xeroderma pigmentosum in man. |
| TextMods | 13: 'NER ' -> 'nucleotide excision repair ' |
| TextRef | info:pmid/19934020#body:46 |
|---|---|
| PubYear | 2009 |
| MedlineTA | J Exp Med |
| Organ | Skin |
| MedLine Reference | 19934020:1045 |
| Sentence | xeroderma pigmentosum may also be caused by defects in other genes in the nucleotide excision repair pathway (XPA, XPB/ERCC3, XPC, XPE/DDB2, XPF/ERCC4, or XPG/ERCC5) or in the polymerase eta gene (xeroderma pigmentosum variant; Masutani et al., 1999; Lehmann, 2003; Kraemer et al., 2007). |
| TextMods | 0: 'XP ' -> 'xeroderma pigmentosum ' 74: 'NER ' -> 'nucleotide excision repair ' 197: 'XP ' -> 'xeroderma pigmentosum ' |