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Journal Abstract Search

581 related items for PubMed ID: 30949161

  • 1.
    ; . PubMed ID:
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  • 2. FCGR2/3 polymorphisms are associated with susceptibility to Kawasaki disease but do not predict intravenous immunoglobulin resistance and coronary artery aneurysms.
    Uittenbogaard P, Netea SA, Tanck MWT, Geissler J, Buda P, Kowalczyk-Domagała M, Okarska-Napierała M, van Stijn D, Tacke CE, US Kawasaki Disease Genetics Consortium, Burgner DP, Shimizu C, Burns JC, Kuipers IM, Kuijpers TW, Nagelkerke SQ.
    Front Immunol; 2024; 15():1323171. PubMed ID: 39359734
    [Abstract] [Full Text] [Related]

  • 3. FCGR2C genotyping by pyrosequencing reveals linkage disequilibrium with FCGR3A V158F and FCGR2A H131R polymorphisms in a Caucasian population.
    Lejeune J, Piègu B, Gouilleux-Gruart V, Ohresser M, Watier H, Thibault G.
    MAbs; 2012; 4(6):784-7. PubMed ID: 23032993
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  • 5. FCGR Genetic Variation in Two Populations From Ecuador Highlands-Extensive Copy-Number Variation, Distinctive Distribution of Functional Polymorphisms, and a Novel, Locally Common, Chimeric FCGR3B/A (CD16B/A) Gene.
    Moraru M, Perez-Portilla A, Al-Akioui Sanz K, Blazquez-Moreno A, Arnaiz-Villena A, Reyburn HT, Vilches C.
    Front Immunol; 2021; 12():615645. PubMed ID: 34108956
    [Abstract] [Full Text] [Related]

  • 6. Genetic Variation in Low-To-Medium-Affinity Fcγ Receptors: Functional Consequences, Disease Associations, and Opportunities for Personalized Medicine.
    Nagelkerke SQ, Schmidt DE, de Haas M, Kuijpers TW.
    Front Immunol; 2019; 10():2237. PubMed ID: 31632391
    [Abstract] [Full Text] [Related]

  • 7. Genetic variations in low-to-medium-affinity Fcγ receptors and autoimmune neutropenia in early childhood in a Danish cohort.
    Kløve-Mogensen K, Steffensen R, Masmas TN, Glenthøj A, Jensen CF, Haunstrup TM, Ratcliffe P, Höglund P, Hasle H, Nielsen KR.
    Int J Immunogenet; 2023 Apr; 50(2):65-74. PubMed ID: 36754570
    [Abstract] [Full Text] [Related]

  • 8. An HIV Vaccine Protective Allele in FCGR2C Associates With Increased Odds of Perinatal HIV Acquisition.
    Ebonwu J, Lassaunière R, Paximadis M, Goosen M, Strehlau R, Gray GE, Kuhn L, Tiemessen CT.
    Front Immunol; 2021 Apr; 12():760571. PubMed ID: 34917081
    [Abstract] [Full Text] [Related]

  • 9. A Case-Control Study on Association of Ulcerative Colitis with FCGR2A Gene Polymorphisms in Chinese Patients.
    Xia SL, Lin DP, Lin QR, Sun L, Wang XQ, Hong WJ, Lin ZJ, Du CC, Jiang Y.
    Genet Test Mol Biomarkers; 2018 Oct; 22(10):607-614. PubMed ID: 30260678
    [Abstract] [Full Text] [Related]

  • 10. Transient and chronic childhood immune thrombocytopenia are distinctly affected by Fc-γ receptor polymorphisms.
    Schmidt DE, Heitink-Pollé KMJ, Laarhoven AG, Bruin MCA, Veldhuisen B, Nagelkerke SQ, Kuijpers TW, Porcelijn L, van der Schoot CE, Vidarsson G, de Haas M.
    Blood Adv; 2019 Jul 09; 3(13):2003-2012. PubMed ID: 31270082
    [Abstract] [Full Text] [Related]

  • 11. [Meta-analyses of the associations of genome-wide association study- linked gene loci with Kawasaki disease].
    Peng Q, Chen CH, Wu Q, Yang Y.
    Zhonghua Er Ke Za Zhi; 2013 Aug 09; 51(8):571-7. PubMed ID: 24225286
    [Abstract] [Full Text] [Related]

  • 12. Nonallelic homologous recombination of the FCGR2/3 locus results in copy number variation and novel chimeric FCGR2 genes with aberrant functional expression.
    Nagelkerke SQ, Tacke CE, Breunis WB, Geissler J, Sins JW, Appelhof B, van den Berg TK, de Boer M, Kuijpers TW.
    Genes Immun; 2015 Sep 09; 16(6):422-9. PubMed ID: 26133275
    [Abstract] [Full Text] [Related]

  • 13. Association of FCGR2A and FCGR2A-FCGR3A haplotypes with susceptibility to giant cell arteritis.
    Morgan AW, Robinson JI, Barrett JH, Martin J, Walker A, Babbage SJ, Ollier WE, Gonzalez-Gay MA, Isaacs JD.
    Arthritis Res Ther; 2006 Sep 09; 8(4):R109. PubMed ID: 16846526
    [Abstract] [Full Text] [Related]

  • 14. Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease.
    Kwon YC, Kim JJ, Yun SW, Yu JJ, Yoon KL, Lee KY, Kil HR, Kim GB, Han MK, Song MS, Lee HD, Ha KS, Sohn S, Ebata R, Hamada H, Suzuki H, Ito K, Onouchi Y, Hong YM, Jang GY, Lee JK, Korean Kawasaki Disease Genetics Consortium.
    PLoS One; 2017 Sep 09; 12(9):e0184248. PubMed ID: 28886140
    [Abstract] [Full Text] [Related]

  • 15. [Single nucleotide polymorphism of FCGR2A gene in Han Chinese children with Kawasaki disease].
    Ji YX, Zhang HY, Lin SX.
    Zhongguo Dang Dai Er Ke Za Zhi; 2013 Mar 09; 15(3):196-200. PubMed ID: 23498761
    [Abstract] [Full Text] [Related]

  • 16. A genetic variant rs1801274 in FCGR2A as a potential risk marker for Kawasaki disease: a case-control study and meta-analysis.
    Duan J, Lou J, Zhang Q, Ke J, Qi Y, Shen N, Zhu B, Zhong R, Wang Z, Liu L, Wu J, Wang W, Gong F, Miao X.
    PLoS One; 2014 Mar 09; 9(8):e103329. PubMed ID: 25093412
    [Abstract] [Full Text] [Related]

  • 17. Association of FCGR2A rs1801274 polymorphism with susceptibility to autoimmune diseases: A meta-analysis.
    Zhang C, Wang W, Zhang H, Wei L, Guo S.
    Oncotarget; 2016 Jun 28; 7(26):39436-39443. PubMed ID: 27270653
    [Abstract] [Full Text] [Related]

  • 18. Distinct haplotype profiles and strong linkage disequilibrium at the MDR1 multidrug transporter gene locus in three ethnic Asian populations.
    Tang K, Ngoi SM, Gwee PC, Chua JM, Lee EJ, Chong SS, Lee CG.
    Pharmacogenetics; 2002 Aug 28; 12(6):437-50. PubMed ID: 12172212
    [Abstract] [Full Text] [Related]

  • 19. Variability at the FCGR locus: characterization in Black South Africans and evidence for ethnic variation in and out of Africa.
    Lassaunière R, Tiemessen CT.
    Genes Immun; 2016 Mar 28; 17(2):93-104. PubMed ID: 26673965
    [Abstract] [Full Text] [Related]

  • 20. Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients.
    Chatzikyriakidou A, Aidinidou L, Giannopoulos A, Papadopoulou-Legbelou K, Kalinderi K, Fidani L.
    Cardiol Young; 2015 Apr 28; 25(4):681-3. PubMed ID: 24775607
    [Abstract] [Full Text] [Related]

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