-
1
-
-
7444265771
-
Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States
-
Kitiyakara C, Eggers P, Kopp JB. Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States. Am J Kidney Dis 2004; 44: 815-825
-
(2004)
Am J Kidney Dis
, vol.44
, pp. 815-825
-
-
Kitiyakara, C.1
Eggers, P.2
Kopp, J.B.3
-
2
-
-
0033152045
-
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity
-
Winn MP, Conlon PJ, Lynn KL, et al. Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity. Genomics 1999; 58: 113-120
-
(1999)
Genomics
, vol.58
, pp. 113-120
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
3
-
-
0029055191
-
Clinical and pathologic features of familial focal segmental glomerulosclerosis
-
Conlon PJ, Butterly D, Albers F, et al. Clinical and pathologic features of familial focal segmental glomerulosclerosis. Am J Kidney Dis 1995; 26: 34-40
-
(1995)
Am J Kidney Dis
, vol.26
, pp. 34-40
-
-
Conlon, P.J.1
Butterly, D.2
Albers, F.3
-
4
-
-
0026332442
-
Sickle cell glomerulopathy with focal segmental glomerulosclerosis
-
Verani RR, Conley SB. Sickle cell glomerulopathy with focal segmental glomerulosclerosis. Child Nephrol Urol 1991; 11: 206-208
-
(1991)
Child Nephrol Urol
, vol.11
, pp. 206-208
-
-
Verani, R.R.1
Conley, S.B.2
-
5
-
-
0032922319
-
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental Glo-merulosclerosis
-
Winn MP, Conlon PJ, Lynn KL, et al. Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental Glo-merulosclerosis. Kidney Int 1999; 55: 1241-1246
-
(1999)
Kidney Int
, vol.55
, pp. 1241-1246
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
6
-
-
33645946089
-
Mutational and biological analysis of alpha-actinin-4 in focal segmental glomerulosclerosis
-
Weins A, Kenlan P, Herbert S, et al. Mutational and biological analysis of alpha-actinin-4 in focal segmental glomerulosclerosis. J Am Soc Nephrol 2005; 16: 3694-3701
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 3694-3701
-
-
Weins, A.1
Kenlan, P.2
Herbert, S.3
-
7
-
-
77649221501
-
Functional analysis of promoter mutations in the ACTN4 and SYNPO genes in focal segmental glomerulosclerosis
-
Dai S, Wang Z, Pan X, et al. Functional analysis of promoter mutations in the ACTN4 and SYNPO genes in focal segmental glomerulosclerosis. Nephrol Dial Transplant 2010; 25: 824-835
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 824-835
-
-
Dai, S.1
Wang, Z.2
Pan, X.3
-
8
-
-
0034034757
-
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant ne-phrotic syndrome
-
Boute N, Gribouval O, Roselli S, et al. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant ne-phrotic syndrome. Nat Genet 2000; 24: 349-354
-
(2000)
Nat Genet
, vol.24
, pp. 349-354
-
-
Boute, N.1
Gribouval, O.2
Roselli, S.3
-
9
-
-
39049163551
-
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome
-
Hinkes B, Vlangos C, Heeringa S, et al. Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome. J Am Soc Nephrol 2008; 19: 365-371
-
(2008)
J Am Soc Nephrol
, vol.19
, pp. 365-371
-
-
Hinkes, B.1
Vlangos, C.2
Heeringa, S.3
-
10
-
-
0036897388
-
NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele
-
Tsukaguchi H, Sudhakar A, Le TC, et al. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. J Clin Invest 2002; 110: 1659-1666
-
(2002)
J Clin Invest
, vol.110
, pp. 1659-1666
-
-
Tsukaguchi, H.1
Sudhakar Le A, T.C.2
-
11
-
-
0034051681
-
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclero-sis
-
Kaplan JM, Kim SH, North KN, et al. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclero-sis. Nat Genet 2000; 24: 251-256
-
(2000)
Nat Genet
, vol.24
, pp. 251-256
-
-
Kaplan, J.M.1
Kim, S.H.2
North, K.N.3
-
12
-
-
20844461826
-
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
-
Winn MP, Conlon PJ, Lynn KL, et al. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science 2005; 308: 1801-1804
-
(2005)
Science
, vol.308
, pp. 1801-1804
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
13
-
-
35848939398
-
NPHS2 variation in sporadic focal segmental glomerulosclerosis
-
McKenzie LM, Hendrickson SL, Briggs WA, et al. NPHS2 variation in sporadic focal segmental glomerulosclerosis. J Am Soc Nephrol 2007; 18: 2987-2995
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2987-2995
-
-
McKenzie, L.M.1
Hendrickson, S.L.2
Briggs, W.A.3
-
14
-
-
58149332840
-
ACTN4 gene mutations and single nucle-otide polymorphisms in idiopathic focal segmental glomerulosclero-sis
-
Dai S, Wang Z, Pan X, et al. ACTN4 gene mutations and single nucle-otide polymorphisms in idiopathic focal segmental glomerulosclero-sis. Nephron Clin Pract 2009; 111: c87-c94
-
(2009)
Nephron Clin Pract
, vol.111
-
-
Dai, S.1
Wang, Z.2
Pan, X.3
-
15
-
-
0037407791
-
Focal and segmental glo-merulosclerosis in mice with podocyte-specific expression of mutant alpha-actinin-4
-
Michaud JL, Lemieux LI, Dube M, et al. Focal and segmental glo-merulosclerosis in mice with podocyte-specific expression of mutant alpha-actinin-4. J Am Soc Nephrol 2003; 14: 1200-1211
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 1200-1211
-
-
Michaud, J.L.1
Lemieux, L.I.2
Dube, M.3
-
16
-
-
0037283752
-
Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis
-
Komatsuda A, Wakui H, Maki N, et al. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis. Ren Fail 2003; 25: 87-93
-
(2003)
Ren Fail
, vol.25
, pp. 87-93
-
-
Komatsuda, A.1
Wakui, H.2
Maki, N.3
-
17
-
-
52449107801
-
Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclero-sis
-
Lowik M, Levtchenko E, Westra D, et al. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclero-sis. Nephrol Dial Transplant 2008; 23: 3146-3151
-
(2008)
Nephrol Dial Transplant
, vol.23
, pp. 3146-3151
-
-
Lowik, M.1
Levtchenko, E.2
Westra, D.3
-
18
-
-
33646406847
-
Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin
-
Huber TB, Kwoh C, Wu H, et al. Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin. J Clin Invest 2006; 116: 1337-1345
-
(2006)
J Clin Invest
, vol.116
, pp. 1337-1345
-
-
Huber, T.B.1
Kwoh, C.2
Wu, H.3
-
19
-
-
16644399642
-
Alpha-actinin-4-mediated FSGS: An inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein
-
Yao J, Le TC, Kos CH, et al. Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein. PLoS Biol 2004; 2: e167
-
(2004)
PLoS Biol
, vol.2
-
-
Yao, J.1
Le Tc Kos, C.H.2
-
20
-
-
10744226566
-
Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome
-
Ruf RG, Lichtenberger A, Karle SM, et al. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. J Am Soc Nephrol 2004; 15: 722-732
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 722-732
-
-
Ruf, R.G.1
Lichtenberger, A.2
Karle, S.M.3
-
21
-
-
69249231160
-
Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations
-
Caridi G, Gigante M, Ravani P, et al. Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations. Clin J Am Soc Nephrol 2009; 4: 1065-1072
-
(2009)
Clin J Am Soc Nephrol
, vol.4
, pp. 1065-1072
-
-
Caridi, G.1
Gigante, M.2
Ravani, P.3
-
22
-
-
0037351063
-
The genetic basis of FSGS and steroid-resistant nephro-sis
-
Pollak MR. The genetic basis of FSGS and steroid-resistant nephro-sis. Semin Nephrol 2003; 23: 141-146
-
(2003)
Semin Nephrol
, vol.23
, pp. 141-146
-
-
Pollak, M.R.1
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