[1] |
Ronco P, Debiec H. Pathophysiological advances in membranous nephropathy: time for a shift in patient's care [J]. Lancet, 2015, 385(9981): 1983-1992.
|
[2] |
Whiting P, Rutjes AW, Reitsma JB, et al. The development of QUADAS: a tool for the quality assessment of studies of diagnostic accuracy included in systematic reviews [J]. BMC Med Res Methodol, 2003, 3(1): 25.
|
[3] |
Wang J, Cui Z, Lu J, et al. Circulating antibodies against thrombospondin type-1 domain-containing 7A in Chinese patients with idiopathic membranous nephropathy [J]. Clin J Am Soc Nephrol, 2017, 12(10): 1642-1651.
|
[4] |
温丽颖,李绍梅,闫喆,等.M型磷脂酶A2受体及1型血小板反应蛋白7A域在成人原发性膜性肾病的表达及其意义[J].中华肾脏病杂志,2016,32(8):561-567.
|
[5] |
Lin L, Wang WM, Pan XX, et al. Biomarkers to detect membranous nephropathy in Chinese patients [J]. Oncotarget, 2016, 7(42): 67868-67879.
|
[6] |
Zhang D, Zou J, Zhang C, et al. Clinical and histological features of phospholipase A2 receptor-associated and thrombospondin type-1 domain-containing 7A-associated idiopathic membranous nephropathy: a single center retrospective study from China [J]. Med Sci Monit, 2018, 24: 5076-5083.
|
[7] |
Hayashi N, Okada K, Matsui Y, et al. Glomerular mannose-binding lectin deposition in intrinsic antigen-related membranous nephropathy [J]. Nephrol Dial Transplant, 2017, 33(5): 832-840.
|
[8] |
Tomas NM, Beck LH Jr, Meyer-Schwesinger C, et al. Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy [J]. N Engl J Med, 2014, 371(24): 2277-2287.
|
[9] |
Iwakura T, Ohashi N, Kato A, et al. Prevalence of enhanced granular expression of thrombospondin type-1 domain-containing 7A in the glomeruli of Japanese patients with idiopathic membranous nephropathy [J]. PLoS One, 2015, 10(9): e0138841.
|
[10] |
L′Imperio V, Pieruzzi F, Sinico RA, et al. Routine immunohistochemical staining in membranous nephropathy: in situ detection of phospholipase A2 receptor and thrombospondin type 1 containing 7A domain [J]. J Nephrol, 2018, 31(4): 543-550.
|
[11] |
Sharma SG, Larsen CP. Tissue staining for THSD7A in glomeruli correlates with serum antibodies in primary membranous nephropathy: a clinicopathological study [J]. Mod Pathol, 2017, 31(4): 616-622.
|
[12] |
Larsen CP, Cossey LN, Beck LH. THSD7A staining of membranous glomerulopathy in clinical practice reveals cases with dual autoantibody positivity [J]. Mod Pathol, 2016, 29(4): 421-426.
|
[13] |
Hoxha E, Beck LH Jr, Wiech T, et al. An indirect immunofluorescence method facilitates detection of thrombospondin type 1 domain-containing 7A-specific antibodies in membranous nephropathy [J]. J Am Soc Nephrol, 2016, 28(2): 520-531.
|
[14] |
Zhang X, Liu S, Tang L, et al. Analysis of pathological data of renal biopsy at one single center in China from 1987 to 2012 [J]. Chin Med J (Engl), 2014, 127(9): 1715-1720.
|
[15] |
Beck LH Jr, Bonegio RG, Lambeau G, et al. M-type phospholipase A2 receptor as target antigen in idiopathic membranous nephropathy [J]. N Engl J Med, 2009, 361(1): 11-21.
|
[16] |
Beck LH Jr. PLA2R and THSD7A: disparate paths to the same disease [J]. J Am Soc Nephrol, 2017, 28(9): 2579-2589.
|
[17] |
Seifert L, Hoxha E, Eichhoff AM, et al. The most N-terminal region of THSD7A is the predominant target for autoimmunity in THSD7A-associated membranous nephropathy [J]. J Am Soc Nephrol, 2018, 29(5): 1536-1548.
|
[18] |
Francis JM, Beck LH Jr, Salant DJ. Membranous nephropathy: a journey from bench to bedside [J]. Am J Kidney Dis, 2016, 68(1): 138-147.
|
[19] |
Ren S, Wu C, Zhang Y, et al. An update on clinical significance of use of THSD7A in diagnosing idiopathic membranous nephropathy: a systematic review and meta-analysis of THSD7A in IMN [J]. Ren Fail, 2018, 40(1): 306-313.
|
[20] |
周广宇,刘锋,张文龙.M型磷脂酶A2受体基因单核苷酸多态性与膜性肾病的相关性[J].中华医学遗传学杂志,2013,30(6):706-710.
|
[21] |
Stahl PR, Hoxha E, Wiech T, et al. THSD7A expression in human cancer [J]. Genes Chromosomes Cancer, 2017, 56(4): 1-55.
|
[22] |
Tomas NM, Hoxha E, Reinicke AT, et al. Autoantibodies against thrombospondin type 1 domain-containing 7A induce membranous nephropathy [J].J Clini Invest, 2016, 126(7): 2519-2532.
|