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The following term was not found in PubMed: 013449002.1
Page 1
Xeroderma Pigmentosum.
Kraemer KH, DiGiovanna JJ, Tamura D. Kraemer KH, et al. 2003 Jun 20 [updated 2022 Mar 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Jun 20 [updated 2022 Mar 24]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301571 Free Books & Documents. Review.
The most common causes of death are skin cancer, neurologic degeneration, and internal cancer. The median age at death in persons with XP with neurodegeneration (29 years) was found to be younger than that in persons with XP without neurodegeneration (37 years). ... …
The most common causes of death are skin cancer, neurologic degeneration, and internal cancer. The median age at death in persons with XP …
Phase III trial comparing capecitabine plus cisplatin versus capecitabine plus cisplatin with concurrent capecitabine radiotherapy in completely resected gastric cancer with D2 lymph node dissection: the ARTIST trial.
Lee J, Lim DH, Kim S, Park SH, Park JO, Park YS, Lim HY, Choi MG, Sohn TS, Noh JH, Bae JM, Ahn YC, Sohn I, Jung SH, Park CK, Kim KM, Kang WK. Lee J, et al. J Clin Oncol. 2012 Jan 20;30(3):268-73. doi: 10.1200/JCO.2011.39.1953. Epub 2011 Dec 19. J Clin Oncol. 2012. PMID: 22184384 Clinical Trial.
The XP/XRT/XP arm received two cycles of XP followed by 45-Gy XRT (capecitabine 1,650 mg/m2 per day for 5 weeks) and two cycles of XP. RESULTS: Of 458 patients, 228 were randomly assigned to the XP arm and 230 to the XP/XRT/XP arm. …
The XP/XRT/XP arm received two cycles of XP followed by 45-Gy XRT (capecitabine 1,650 mg/m2 per day for 5 weeks) and tw …
Xeroderma pigmentosum-Cockayne syndrome complex.
Natale V, Raquer H. Natale V, et al. Orphanet J Rare Dis. 2017 Apr 4;12(1):65. doi: 10.1186/s13023-017-0616-2. Orphanet J Rare Dis. 2017. PMID: 28376890 Free PMC article. Review.
There are four groups in XP-CS, and classification was available for 42 patients. Twenty-one were in the XP-G complementation group, 13 in XP-D, 5 in XP-B, and 3 in XP-F. ...However, one intriguing finding was that cancer incidence was lower in …
There are four groups in XP-CS, and classification was available for 42 patients. Twenty-one were in the XP-G complementation …
Xylan Plastic.
Jia S, Lv Z, Rao J, Lü B, Chen G, Bian J, Li M, Peng F. Jia S, et al. ACS Nano. 2023 Jul 25;17(14):13627-13637. doi: 10.1021/acsnano.3c02327. Epub 2023 Jul 13. ACS Nano. 2023. PMID: 37439501
Dynamic mechanical analysis (DMA) characterizations confirmed that XP is thermoplastic and can be hot formed. Additionally, the reversible hydrogen bond interaction between xylan chains could be simply regulated by water molecules, rendering XP readily transformed a …
Dynamic mechanical analysis (DMA) characterizations confirmed that XP is thermoplastic and can be hot formed. Additionally, the rever …
Sunlight, Vitamin D, and Xeroderma Pigmentosum.
Martens MC, Emmert S, Boeckmann L. Martens MC, et al. Adv Exp Med Biol. 2020;1268:319-331. doi: 10.1007/978-3-030-46227-7_16. Adv Exp Med Biol. 2020. PMID: 32918226 Review.
As UV radiation plays a critical role in the photosynthesis of vitamin D, stringent sun protection, as recommended for xeroderma pigmentosum (XP) patients, may impact their vitamin D levels.XP is a rare autosomal recessive disorder with a worldwide prevalence of 1 i …
As UV radiation plays a critical role in the photosynthesis of vitamin D, stringent sun protection, as recommended for xeroderma pigmentosum …
[Xeroderma pigmentosum].
Takeuchi S. Takeuchi S. Nihon Rinsho. 2000 Jul;58(7):1496-500. Nihon Rinsho. 2000. PMID: 10921330 Review. Japanese.
There are eight different complementation groups in XP; groups A through G and a variant(XP-V). XP-A through XP-G have a defect in nucleotide excision repair(NER), while XP-V has a defect in translesion DNA synthesis. ...In this review, the pres …
There are eight different complementation groups in XP; groups A through G and a variant(XP-V). XP-A through XP- …
Meta-analysis of three randomized trials of capecitabine plus cisplatin (XP) versus S-1 plus cisplatin (SP) as first-line treatment for advanced gastric cancer.
Nishikawa K, Kawakami H, Shimokawa T, Fujitani K, Tamura S, Endo S, Kobayashi M, Kawada J, Kurokawa Y, Tsuburaya A, Yoshikawa T, Sakamoto J, Satoh T; for HERBIS-2, HERBIS-4A, XParTS I. I. study investigators. Nishikawa K, et al. Int J Clin Oncol. 2023 Nov;28(11):1501-1510. doi: 10.1007/s10147-023-02402-1. Epub 2023 Aug 27. Int J Clin Oncol. 2023. PMID: 37634209
For the differentiated type, OS was significantly longer in the SP group (13.2 months) than in the XP group (11.1 months) (HR, 0.549; P = 0.019). For the undifferentiated type, OS was similar in the SP group (14.2 months) and in the XP group (12.4 months) (HR, 0.868 …
For the differentiated type, OS was significantly longer in the SP group (13.2 months) than in the XP group (11.1 months) (HR, 0.549; …
Genetic insight into putative causes of xanthelasma palpebrarum: a Mendelian randomization study.
Hu W, Liu Y, Lian C, Lu H. Hu W, et al. Front Immunol. 2024 Mar 27;15:1347112. doi: 10.3389/fimmu.2024.1347112. eCollection 2024. Front Immunol. 2024. PMID: 38601164 Free PMC article.
Xanthelasma palpebrarum (XP) is the most common form of cutaneous xanthoma, with a prevalence of 1.1%~4.4% in the population. ...In conclusion, this study identified plasma cholesterol, LDL-C, and 12 circulating proteins to be putative causal factors for XP, highlig …
Xanthelasma palpebrarum (XP) is the most common form of cutaneous xanthoma, with a prevalence of 1.1%~4.4% in the population. ...In c …
Xeroderma pigmentosum: beyond skin cancer.
Lichon V, Khachemoune A. Lichon V, et al. J Drugs Dermatol. 2007 Mar;6(3):281-8. J Drugs Dermatol. 2007. PMID: 17373189 Review.
Xeroderma pigmentosum (XP) is a rare, autosomal-recessive inherited disease that is found worldwide at a frequency of approximately 1:250,000. ...We present a review of the history, clinical manifestations, pathogenesis, diagnosis, and treatment of XP....
Xeroderma pigmentosum (XP) is a rare, autosomal-recessive inherited disease that is found worldwide at a frequency of approximately 1 …
Xeroderma Pigmentosum: A Model for Human Premature Aging.
Rizza ERH, DiGiovanna JJ, Khan SG, Tamura D, Jeskey JD, Kraemer KH. Rizza ERH, et al. J Invest Dermatol. 2021 Apr;141(4S):976-984. doi: 10.1016/j.jid.2020.11.012. Epub 2021 Jan 9. J Invest Dermatol. 2021. PMID: 33436302 Free PMC article. Review.
Poikiloderma, atypical lentigines, and skin cancers, the primary cutaneous features of XP, occur in the general population but at a much older age. Patients with XP also exhibit ocular changes secondary to premature photoaging, including ocular surface tumors and pt …
Poikiloderma, atypical lentigines, and skin cancers, the primary cutaneous features of XP, occur in the general population but at a m …
8,680 results