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Träfflista för sökning "WFRF:(Vivian U.) srt2:(2017)"

Sökning: WFRF:(Vivian U.) > (2017)

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Numrering	Referens	Omslagsbild	Hitta
1.	Ahmad, T, et al. (författare) In-hospital clinical outcomes after upper gastrointestinal surgery: Data from an international observational study 2017 Ingår i: European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. - : Elsevier BV. - 1532-2157 .- 0748-7983. ; 43:12, s. 2324-2332 Tidskriftsartikel (refereegranskat)
2.	Ahmad, T, et al. (författare) Use of failure-to-rescue to identify international variation in postoperative care in low-, middle- and high-income countries: a 7-day cohort study of elective surgery 2017 Ingår i: British journal of anaesthesia. - : Elsevier BV. - 1471-6771 .- 0007-0912. ; 119:2, s. 258-266 Tidskriftsartikel (refereegranskat)
3.	Sharma, Rohan, et al. (författare) Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjogrens Syndrome 2017 Ingår i: Arthritis & Rheumatology. - : WILEY. - 2326-5191 .- 2326-5205. ; 69:11, s. 2187-2192 Tidskriftsartikel (refereegranskat)abstract Objective. Sjogrens syndrome (SS) and systemic lupus erythematosus (SLE) are related by clinical and serologic manifestations as well as genetic risks. Both diseases are more commonly found in women than in men, at a ratio of similar to 10 to 1. Common X chromosome aneuploidies, 47,XXY and 47,XXX, are enriched among men and women, respectively, in either disease, suggesting a dose effect on the X chromosome. Methods. We examined cohorts of SS and SLE patients by constructing intensity plots of X chromosome single-nucleotide polymorphism alleles, along with determining the karyotype of selected patients. Results. Among similar to 2,500 women with SLE, we found 3 patients with a triple mosaic, consisting of 45,X/46,XX/47,XXX. Among similar to 2,100 women with SS, 1 patient had 45,X/46,XX/47,XXX, with a triplication of the distal p arm of the X chromosome in the 47,XXX cells. Neither the triple mosaic nor the partial triplication was found among the controls. In another SS cohort, we found a mother/daughter pair with partial triplication of this same region of the X chromosome. The triple mosaic occurs in similar to 1 in 25,000-50,000 live female births, while partial triplications are even rarer. Conclusion. Very rare X chromosome abnormalities are present among patients with either SS or SLE and may inform the location of a gene(s) that mediates an X dose effect, as well as critical cell types in which such an effect is operative.

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Typ av publikation: tidskriftsartikel (3)

Typ av innehåll: refereegranskat (3)

Författare/redaktör: Bai, Y. (2); Brown, J. (2); Chen, C. (2); Chen, H. (2); Chen, S. (2); Francis, D. (2); visa fler...; Huang, Y. (2); Li, B. (2); Li, H. (2); Liu, B. (2); Liu, M. (2); Liu, Y. (2); March, L. (2); Pinder, A. (2); Sanchez, A. (2); Silva, J. (2); Walker, R. (2); Wang, F. (2); Wang, J. (2); Webb, S. (2); White, S. (2); Williams, S. (2); Wilson, A. (2); Xu, L. (2); Yang, Y. (2); Zhang, H. (2); Zhang, J. (2); Zhang, L. (2); Zhu, Y. (2); Brenner, L. (2); Simon, D. (2); Zhou, C. (2); Brown, G. (2); Ellis, K. (2); Rose, A. (2); Zhao, L. (2); Ahmad, A. (2); He, M. (2); Ryan, P. (2); Schmitz, M. (2); Zhao, T. (2); Gupta, A. (2); Joseph, J. (2); Kennedy, J. (2); Li, J. (2); Yuan, J. (2); Zhang, Q. (2); Ren, Y. (2); Martin, J. (2); Alexander, M. (2); visa färre...

Lärosäte: Karolinska Institutet (3); Uppsala universitet (1); Linköpings universitet (1); Lunds universitet (1)

Språk: Engelska (3)

Forskningsämne (UKÄ/SCB): Medicin och hälsovetenskap (3)

År: 2017 (3)Ta bort avgränsningen

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