The 32 references in paper E. Petrosyan K., A. Tsygin N., A. Shestakov E., V. Nosikov V., Э. Петросян К., А. Цыгин Н., А. Шестаков Е., В. Носиков В. (2006) “ГЕНЕТИЧЕСКИЕ МАРКЕРЫ НЕФРОТИЧЕСКОГО СИНДРОМА У ДЕТЕЙ // GENETIC MARKERS OF NEPHROTIC SYNDROME IN CHILDREN” / spz:neicon:nefr:y:2006:i:3:p:48-54

1
Churg J, Habib R, and White R.H. Pathology of the nephrotic sendrome in children: a report for the International Study of Kidney Disease in Children. Lancet I 1970; 1299-1302
(check this in PDF content)
2
White RH, Glasgow EF, Mills RJ. Clinicopathological study of nephrotic syndrome in childhood. Lancet I 1970; 1353-1359
(check this in PDF content)
3
Kobayashi Y, Arakawa H, Suzuki M et al. Polymorphisms of interleukin-4-related genes in Japanese children with minimal change nephrotic syndrome. Am J Kidney Dis 2003; 42: 271-276
(check this in PDF content)
4
Acharya B, Shirakawa T, Pungky A et al. Polymorphism of the IL-4, IL-13 and signal transducer and activator transcription 6 genes in Indonesian children with minimal change nephrotic syndrome. Am J Nephrol 2005; 25: 30-35
(check this in PDF content)
5
Parry RG, Gillespie KM, Parhnam A et al. Interleukin-4 and interleikin-4 receptor polymorphism in minimal change nephropathy. Clin Sci 1999; 96: 665-668
(check this in PDF content)
6
Glassock RJ, Adler SG, Ward HJ et al. Primary glomerular diseases. In: The Kidney. BM.Brenner, FC.Rector, eds., W.B.Saunders Co., Philadelphia, 1991; 1182-1279
(check this in PDF content)
7
Shirata I, Hosser H, Kimura K et al. The development of focal segmental glomerulosclerosis in Masugi nephritis is based on progressive podocyte damage. Virchows Arch 1996; 429: 255-273
(check this in PDF content)
8
Shankland SJ, Floege J, Thomas SE et al. Cyclin kinase inhibitors are increased during experimental membranous nephropathy: Potential role in limiting glomerular epithelial cell proliferation in vivo. Kidney Int 1997; 52: 404-413
(check this in PDF content)
9
Kestila M, Lenkkeri U, Mannikko M et al. Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome. Mol Cell 1998; 1:575-582
(check this in PDF content)
10
Lahdenkari AT, Kestila M, Holmberg C et al. Nephrin gene (NPHS1) in patients with minimal change nephritic syndrome (MCNS). Kidney Int 2004; 65: 1856-1863
(check this in PDF content)
11
Huber TB, Simons M, Hartleben B et al. Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to the lipid raft microdomains. Hum Mol Genet 2003; 12:3397-3405
(check this in PDF content)
12
Weber S, Gribouval O, Esquivel EL et al. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephritic syndrome and low post-transplant recurrence. Kidney Int 2004; 66:571-579
(check this in PDF content)
13
Рябов СИ. Нефротический синдром. Гиппократ, СПб.,1992; 352
(check this in PDF content)
14
Шулутко БИ. Вторичные нефропатии. Медицина, М., 1987;208
(check this in PDF content)
15
Fuchshuber A, Mehls O. Familial steroid-resistant nephrotic syndromes: recent advances. Nephrol Dial Transplant 2000; 15: 1897-1900
(check this in PDF content)
16
Ahmad H, Tejani A. Predictive value of repeat renal biopsies in children with nephrotic syndrome. Nephron 2000; 84: 342-346
(check this in PDF content)
17
Wernerson A, Duner F, Pettterson E et al. Altered ultructural distribuition of nephrin in minimal change nephrotic syndrome. Nephrol Dial Transplant 2003; 18: 70-76
(check this in PDF content)
18
Regele HM, Fillipovic E, Langer B et al. Glomerular expression of dystroglycans is reduced in minimal change nephrosis but not in focal segmental glomerulosclerosis. J Am Soc Nephrol 2000; 11: 403-412
(check this in PDF content)
19
Schmid H, Henger A, Cohen CD et al. Gtne expression profiles of podocyte-associated molecules as diagnostic markers in acquired proteinuric diseases. J Am Soc Nephrol
(check this in PDF content)
20
3; 14: 2958-2966 20. Romaggnani S. Th1/Th2 paradigm. Immunol Today 1997; 18: 293-266
(check this in PDF content)
21
Heinzman A, Jerkic SP, Ganter K et al. Genetic variants of IL-13 signalling and human asthma and atopy. Hum Mol Genet 2000; 9: 549-559
(check this in PDF content)
22
Kruse S, Japha T, Tedner M et al.The polymorphism S503P and Q576R in interleukin-4 receptor a gene are associated with atopy and influence the signal transduction. Immunology 1999; 96: 365-371
(check this in PDF content)
23
Liu X, Beaty TH, Deindl P. Association between total serum IgE levels and the 6 potentially functional variants within the genes IL-4, IL-13 and IL-4RA in German children: The German Multicenter Atopy Study. J Allergy Clin Immunol 2003;112: 382-388
(check this in PDF content)
24
Arima K, Imeshita-Suyama R, Sakata Y et al. Upregulation of IL-13 concentration in vivo by the IL-13 variant associated with bronchial asthma. J Allergy Clin Immunol 2002; 105: 980-987
(check this in PDF content)
25
Kawashima T, Noguchi E, Arinami T et al. Linkage and association of an interleukin-4 gene polymorphism with atopic dermatitis in Japanese families. J Med Genet 1998; 35: 502­ 504
(check this in PDF content)
26
Doublier S, Ruotsalainen V, Salvidio G et al. Nephrin redistribution on podocytes is a potential mechanism for proteinuria in patients with primary acquired nephrotic syndrome. Am J Pathol 2001; 158:1723-1731
(check this in PDF content)
27
Furness PN, Hall LL, Shaw JA, Pringle JH. Glomerular expression of nephrin is decreased in acquired human nephrotic syndrome. Nephrol Dial Transplant 1999; 14: 1234-1237
(check this in PDF content)
28
Kim BK, Hong HK, Kim JH, Lee HS. Differential expression of nephrin in acquired human proteinuric diseases. Am J Kidney Dis 2002; 40: 964-973
(check this in PDF content)
29
Kawachi H, Koike H, Kurihara Het al. Cloning of rat nephrin: expression in developing glomeruli and in proteinuric states. Kidney Int 2000; 57: 1949-1961
(check this in PDF content)
30
Luimula P, Ahola H, Wang SX et al. Nephrin in experimental glomerular disease. Kidney Int 2000; 58: 1461­ 1468
(check this in PDF content)
31
Yuan H, Takeuchi E, Taylor GA et al. Nephrin dissociates from actin, and its expression is reduced in early experimental membranous nephropathy. J Am Soc Nephrol 2002; 13: 946­ 956
(check this in PDF content)
32
Lahdenkari AT, Suvanto M, Kajantie E et al. Clinical features and outcome of chilhood minimal change nephrotic syndrome: is genetics involved? Pediatr Nephrol 2005; 20: 1073­ 1080 Поступила в редакцию 21.04.2006 г.
(check this in PDF content)