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Journal Abstract Search
136 related items for PubMed ID: 36754570
1. 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]
2. Association between human leukocyte antigens (HLAs) and human neutrophil antigens (HNAs) and autoimmune neutropenia of infancy in Danish patients. Nielsen KR, Bojsen SR, Masmas TN, Fjordside AL, Baech J, Haunstrup TM, Steffensen R. Pediatr Allergy Immunol; 2021 May; 32(4):756-761. PubMed ID: 33421202 [Abstract] [Full Text] [Related]
3. FCGR2B gene polymorphism rather than FCGR2A, FCGR3A and FCGR3B is associated with anti-GBM disease in Chinese. Zhou XJ, Lv JC, Yu L, Cui Z, Zhao J, Yang R, Han J, Hou P, Zhao MH, Zhang H. Nephrol Dial Transplant; 2010 Jan; 25(1):97-101. PubMed ID: 19640933 [Abstract] [Full Text] [Related]
4. Extensive Ethnic Variation and Linkage Disequilibrium at the FCGR2/3 Locus: Different Genetic Associations Revealed in Kawasaki Disease. Nagelkerke SQ, Tacke CE, Breunis WB, Tanck MWT, Geissler J, Png E, Hoang LT, van der Heijden J, Naim ANM, Yeung RSM, Levin ML, Wright VJ, Burgner DP, Ponsonby AL, Ellis JA, Cimaz R, Shimizu C, Burns JC, Fijnvandraat K, van der Schoot CE, van den Berg TK, de Boer M, Davila S, Hibberd ML, Kuijpers TW, International Kawasaki Disease Genetics Consortium. Front Immunol; 2019 Jan; 10():185. PubMed ID: 30949161 [Abstract] [Full Text] [Related]
7. HNA-1d: a new human neutrophil antigen located on Fcγ receptor IIIb associated with neonatal immune neutropenia. Reil A, Sachs UJ, Siahanidou T, Flesch BK, Bux J. Transfusion; 2013 Oct; 53(10):2145-51. PubMed ID: 23347194 [Abstract] [Full Text] [Related]
9. Fcgamma receptor gene polymorphisms in Japanese patients with systemic lupus erythematosus: contribution of FCGR2B to genetic susceptibility. Kyogoku C, Dijstelbloem HM, Tsuchiya N, Hatta Y, Kato H, Yamaguchi A, Fukazawa T, Jansen MD, Hashimoto H, van de Winkel JG, Kallenberg CG, Tokunaga K. Arthritis Rheum; 2002 May; 46(5):1242-54. PubMed ID: 12115230 [Abstract] [Full Text] [Related]
10. Analysis of Fcgamma receptor haplotypes in rheumatoid arthritis: FCGR3A remains a major susceptibility gene at this locus, with an additional contribution from FCGR3B. Morgan AW, Barrett JH, Griffiths B, Subramanian D, Robinson JI, Keyte VH, Ali M, Jones EA, Old RW, Ponchel F, Boylston AW, Situnayake RD, Markham AF, Emery P, Isaacs JD. Arthritis Res Ther; 2006 May; 8(1):R5. PubMed ID: 16356189 [Abstract] [Full Text] [Related]
12. Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes. Franke L, el Bannoudi H, Jansen DT, Kok K, Trynka G, Diogo D, Swertz M, Fransen K, Knevel R, Gutierrez-Achury J, Ärlestig L, Greenberg JD, Kremer J, Pappas DA, Kanterakis A, Weersma RK, van der Helm-van Mil AH, Guryev V, Rantapää-Dahlqvist S, Gregersen PK, Plenge RM, Wijmenga C, Huizinga TW, Ioan-Facsinay A, Toes RE, Zhernakova A. Eur J Hum Genet; 2016 Feb; 24(2):263-70. PubMed ID: 25966632 [Abstract] [Full Text] [Related]
13. Association of Fcγ receptor IIB polymorphism with cryptococcal meningitis in HIV-uninfected Chinese patients. Hu XP, Wu JQ, Zhu LP, Wang X, Xu B, Wang RY, Ou XT, Weng XH. PLoS One; 2012 Feb; 7(8):e42439. PubMed ID: 22879986 [Abstract] [Full Text] [Related]
14. Genetic polymorphisms in IL-2, IL-10 and FOXP3 are associated with autoimmune neutropenia in early childhood and autoantibody specificity in a Danish cohort. Kløve-Mogensen K, Steffensen R, Masmas TN, Glenthøj A, Jensen CF, Ratcliffe P, Höglund P, Hasle H, Nielsen KR, Haunstrup TM. Scand J Immunol; 2024 Aug; 100(2):e13374. PubMed ID: 38750640 [Abstract] [Full Text] [Related]
16. Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus. Mueller M, Barros P, Witherden AS, Roberts AL, Zhang Z, Schaschl H, Yu CY, Hurles ME, Schaffner C, Floto RA, Game L, Steinberg KM, Wilson RK, Graves TA, Eichler EE, Cook HT, Vyse TJ, Aitman TJ. Am J Hum Genet; 2013 Jan 10; 92(1):28-40. PubMed ID: 23261299 [Abstract] [Full Text] [Related]
17. Functional Fcgamma receptor polymorphisms are associated with human allergy. Wu J, Lin R, Huang J, Guan W, Oetting WS, Sriramarao P, Blumenthal MN. PLoS One; 2014 Jan 10; 9(2):e89196. PubMed ID: 24586589 [Abstract] [Full Text] [Related]
18. 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 Jan 10; 10():2237. PubMed ID: 31632391 [Abstract] [Full Text] [Related]
19. High-resolution HLA genotyping identifies risk alleles in both class I and II for primary autoimmune neutropenia in early childhood in a Danish cohort. Kløve-Mogensen K, Haunstrup TM, Masmas TN, Glenthøj A, Höglund P, Hasle H, Nielsen KR, Steffensen R. HLA; 2024 Mar 10; 103(3):e15429. PubMed ID: 38450943 [Abstract] [Full Text] [Related]
20. Copy number, linkage disequilibrium and disease association in the FCGR locus. Niederer HA, Willcocks LC, Rayner TF, Yang W, Lau YL, Williams TN, Scott JA, Urban BC, Peshu N, Dunstan SJ, Hien TT, Phu NH, Padyukov L, Gunnarsson I, Svenungsson E, Savage CO, Watts RA, Lyons PA, Clayton DG, Smith KG. Hum Mol Genet; 2010 Aug 15; 19(16):3282-94. PubMed ID: 20508037 [Abstract] [Full Text] [Related] Page: [Next] [New Search]