-
1
-
-
0030687596
-
Changing etiologies of unexplained adult nephrotic syndrome: A comparison of renal biopsy findings from 1976-1979 and 1995-1997
-
M. Haas, S.M. Meehan, T.G. Karrison Changing etiologies of unexplained adult nephrotic syndrome A comparison of renal biopsy findings from 1976-1979 and 1995-1997 Am J Kidney Dis 30 1997 621 631
-
(1997)
Am J Kidney Dis
, vol.30
, pp. 621-631
-
-
Haas, M.1
Meehan, S.M.2
Karrison, T.G.3
-
2
-
-
7444265771
-
Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States
-
C. Kitiyakara, P. Eggers, J.B. Kopp Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States Am J Kidney Dis 44 2004 815 825
-
(2004)
Am J Kidney Dis
, vol.44
, pp. 815-825
-
-
Kitiyakara, C.1
Eggers, P.2
Kopp, J.B.3
-
4
-
-
12444328765
-
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin
-
R. Bertelli, G. Fabrizio, G. Caridi Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin Am J Kidney Dis 41 2003 1314 1321
-
(2003)
Am J Kidney Dis
, vol.41
, pp. 1314-1321
-
-
Bertelli, R.1
Fabrizio, G.2
Caridi, G.3
-
6
-
-
0028358714
-
Primary focal segmental glomerulosclerosis: Clinical course and response to therapy
-
S.M. Korbet, M.M. Schwartz, E.J. Lewis Primary focal segmental glomerulosclerosis Clinical course and response to therapy Am J Kidney Dis 23 1994 773 783
-
(1994)
Am J Kidney Dis
, vol.23
, pp. 773-783
-
-
Korbet, S.M.1
Schwartz, M.M.2
Lewis, E.J.3
-
7
-
-
0016266173
-
Pathogenesis of lipoid nephrosis: A disorder of T-cell function
-
R.J. Shaloub Pathogenesis of lipoid nephrosis A disorder of T-cell function Lancet 2 1974 556 560
-
(1974)
Lancet
, vol.2
, pp. 556-560
-
-
Shaloub, R.J.1
-
8
-
-
0035458322
-
Recurrence of idiopathic nephrotic syndrome after renal transplantation
-
J.R. Hoyer, R.L. Vernier, J.S. Najarian Recurrence of idiopathic nephrotic syndrome after renal transplantation 1972 J Am Soc Nephrol 12 2001 1994 2002
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 1994-2002
-
-
Hoyer, J.R.1
Vernier, R.L.2
Najarian, J.S.3
-
9
-
-
0021207322
-
Increased urinary protein excretion in the rat produced by serum from a patient with recurrent focal glomerular sclerosis after renal transplantation
-
S.W. Zimmerman Increased urinary protein excretion in the rat produced by serum from a patient with recurrent focal glomerular sclerosis after renal transplantation Clin Nephrol 22 1984 32 38
-
(1984)
Clin Nephrol
, vol.22
, pp. 32-38
-
-
Zimmerman, S.W.1
-
10
-
-
0027979377
-
Effect of plasma protein adsorption on protein excretion on protein excretion in kidney transplant recipients with recurrent nephrotic syndrome
-
J. Dantal, E. Bigot, W. Bogers Effect of plasma protein adsorption on protein excretion on protein excretion in kidney transplant recipients with recurrent nephrotic syndrome N Engl J Med 330 1994 7 14
-
(1994)
N Engl J Med
, vol.330
, pp. 7-14
-
-
Dantal, J.1
Bigot, E.2
Bogers, W.3
-
11
-
-
13344285352
-
Circulating factor increasing glomerular permeability in recurrent focal segmental glomerulosclerosis
-
V.J. Savin, R. Sharma, M. Smarma Circulating factor increasing glomerular permeability in recurrent focal segmental glomerulosclerosis N Engl J Med 334 1996 878 888
-
(1996)
N Engl J Med
, vol.334
, pp. 878-888
-
-
Savin, V.J.1
Sharma, R.2
Smarma, M.3
-
12
-
-
0028278929
-
Plasmapheresis reduces proteinuria and serum capacity to injure glomeruli in patients with recurrent focal glomerulosclerosis
-
M.L. Artero, R. Sharma, V.J. Savin Plasmapheresis reduces proteinuria and serum capacity to injure glomeruli in patients with recurrent focal glomerulosclerosis Am J Kidney Dis 23 1994 574 581
-
(1994)
Am J Kidney Dis
, vol.23
, pp. 574-581
-
-
Artero, M.L.1
Sharma, R.2
Savin, V.J.3
-
13
-
-
0031871947
-
Plasma immunoadsorption treatment in patients with primary focal and segmental glomerulosclerosis
-
M. Haas, Y. Godfrin, R. Oberbauer Plasma immunoadsorption treatment in patients with primary focal and segmental glomerulosclerosis Nephrol Dial Transplant 13 1998 2013 2016
-
(1998)
Nephrol Dial Transplant
, vol.13
, pp. 2013-2016
-
-
Haas, M.1
Godfrin, Y.2
Oberbauer, R.3
-
14
-
-
0031750931
-
Antihuman immunoglobulin affinity immunoadsorption strongly decreases proteinuria in patients with relapsing nephrotic syndrome
-
J. Dantal, Y. Godfrin, R. Koll Antihuman immunoglobulin affinity immunoadsorption strongly decreases proteinuria in patients with relapsing nephrotic syndrome J Am Soc Nephrol 9 1998 1709 1715
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 1709-1715
-
-
Dantal, J.1
Godfrin, Y.2
Koll, R.3
-
15
-
-
0033813660
-
Plasmapheresis treatment for recurrent focal sclerosis in pediatric renal allografts
-
S.M. Greenstein, M. Delrio, E. Ong Plasmapheresis treatment for recurrent focal sclerosis in pediatric renal allografts Pediatr Nephrol 16 2000 1061 1065
-
(2000)
Pediatr Nephrol
, vol.16
, pp. 1061-1065
-
-
Greenstein, S.M.1
Delrio, M.2
Ong, E.3
-
16
-
-
0035667857
-
Long term plasmapheresis and protein a column treatment of recurrent FSGS
-
A. Belson, P.D. Yorgin, A.Y. Al-Uzri Long term plasmapheresis and protein A column treatment of recurrent FSGS Pediatr Nephrol 16 2001 898 900
-
(2001)
Pediatr Nephrol
, vol.16
, pp. 898-900
-
-
Belson, A.1
Yorgin, P.D.2
Al-Uzri, A.Y.3
-
17
-
-
0034759825
-
Plasmapheresis-induced remission in otherwise therapy-resistant FSGS
-
A.K. Vecsei, T. Muller, E.C. Schratzberger Plasmapheresis-induced remission in otherwise therapy-resistant FSGS Pediatr Nephrol 16 2001 898 900
-
(2001)
Pediatr Nephrol
, vol.16
, pp. 898-900
-
-
Vecsei, A.K.1
Muller, T.2
Schratzberger, E.C.3
-
18
-
-
0035868347
-
Effect of pre- and postoperative plasmapheresis on post-transplant recurrence of focal segmental glomerulosclerosis in children
-
T. Ohta, H. Kawaguchi, M. Hattori Effect of pre- and postoperative plasmapheresis on post-transplant recurrence of focal segmental glomerulosclerosis in children Transplantation 71 2001 628 633
-
(2001)
Transplantation
, vol.71
, pp. 628-633
-
-
Ohta, T.1
Kawaguchi, H.2
Hattori, M.3
-
19
-
-
0037350945
-
Permeability factors in focal segmental glomerulosclerosis
-
V.J. Savin, E.T. McCarthy, M. Sharma Permeability factors in focal segmental glomerulosclerosis Semin Nephrol 23 2003 147 160
-
(2003)
Semin Nephrol
, vol.23
, pp. 147-160
-
-
Savin, V.J.1
McCarthy, E.T.2
Sharma, M.3
-
20
-
-
0033052191
-
"the FSGS factor" enrichment and in vivo effect of activity from focal segmental glomerulosclerosis plasma
-
M. Sharma, R. Sharma, E.T. McCarthy "The FSGS factor" enrichment and in vivo effect of activity from focal segmental glomerulosclerosis plasma J Am Soc Nephrol 10 1999 552 561
-
(1999)
J Am Soc Nephrol
, vol.10
, pp. 552-561
-
-
Sharma, M.1
Sharma, R.2
McCarthy, E.T.3
-
21
-
-
0037083876
-
Proteinuria after injection of human focal segmental glomerulosclerosis factor
-
M. Sharma, R. Sharma, S.R. Reddy Proteinuria after injection of human focal segmental glomerulosclerosis factor Transplantation 73 2002 366 372
-
(2002)
Transplantation
, vol.73
, pp. 366-372
-
-
Sharma, M.1
Sharma, R.2
Reddy, S.R.3
-
22
-
-
3042850481
-
Proteinuria in rats induced by serum from patients with collapsing glomerulopathy
-
M. Del Carmen Avila-Casado, I. Perez-Torres, A. Auron Proteinuria in rats induced by serum from patients with collapsing glomerulopathy Kidney Int 66 2004 133 143
-
(2004)
Kidney Int
, vol.66
, pp. 133-143
-
-
Del Carmen Avila-Casado, M.1
Perez-Torres, I.2
Auron, A.3
-
23
-
-
0020587151
-
Nephrotic syndrome in spontaneous thymoma rats, Buffalo/Mna
-
F. Kato, M. Watanabe, M. Matsuyama Nephrotic syndrome in spontaneous thymoma rats, Buffalo/Mna Biomed Res 4 1983 105 110
-
(1983)
Biomed Res
, vol.4
, pp. 105-110
-
-
Kato, F.1
Watanabe, M.2
Matsuyama, M.3
-
24
-
-
0022650116
-
Sclerotic lesions in the glomeruli of Buffalo/Mna rats
-
T. Nakamura, T. Oite, F. Shimizu Sclerotic lesions in the glomeruli of Buffalo/Mna rats Nephron 43 1986 50 55
-
(1986)
Nephron
, vol.43
, pp. 50-55
-
-
Nakamura, T.1
Oite, T.2
Shimizu, F.3
-
25
-
-
0036180306
-
Extrarenal effects on the pathogenesis and relapse of idiopathic nephrotic syndrome in Buffalo/Mna rats
-
L. Le Berre, Y. Godfrin, E. Gunther Extrarenal effects on the pathogenesis and relapse of idiopathic nephrotic syndrome in Buffalo/Mna rats J Clin Invest 109 2002 491 498
-
(2002)
J Clin Invest
, vol.109
, pp. 491-498
-
-
Le Berre, L.1
Godfrin, Y.2
Gunther, E.3
-
27
-
-
0033365398
-
Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome.Finnish type, in the old order Mennonites [letter]
-
S. Bolk, E.G. Puffenberger, J. Hudson Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome.Finnish type, in the old order Mennonites [letter] Am J Hum Genet 65 1999 1785 1790
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1785-1790
-
-
Bolk, S.1
Puffenberger, E.G.2
Hudson, J.3
-
28
-
-
0028329864
-
Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19
-
M. Kestilä, U. Lenkkeri, M. Männikkö Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19 Am J Hum Genet 54 1994 757 764
-
(1994)
Am J Hum Genet
, vol.54
, pp. 757-764
-
-
Kestilä, M.1
Lenkkeri, U.2
Männikkö, M.3
-
29
-
-
0032015551
-
Positionally cloned gene for a novel glomerular protein - Nephrin - Is mutated in congenital nephrotic syndrome
-
M. Kestilä, U. Lenkkeri, M. Männikkö Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome Mol Cell 1 1998 575 582
-
(1998)
Mol Cell
, vol.1
, pp. 575-582
-
-
Kestilä, M.1
Lenkkeri, U.2
Männikkö, M.3
-
30
-
-
0033366679
-
Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations
-
U. Lenkkeri, M. Männikkö, P. McCready Structure of the gene for congenital nephrotic syndrome of the Finnish type (NPHS1) and characterization of mutations Am J Hum Genet 64 1999 51 61
-
(1999)
Am J Hum Genet
, vol.64
, pp. 51-61
-
-
Lenkkeri, U.1
Männikkö, M.2
McCready, P.3
-
31
-
-
0032861101
-
Nephrin localizes to the slit pore of the glomerular epithelial cell
-
L.B. Holzman, P.L. St. John, I.A. Kovari Nephrin localizes to the slit pore of the glomerular epithelial cell Kidney Int 56 1999 1481 1491
-
(1999)
Kidney Int
, vol.56
, pp. 1481-1491
-
-
Holzman, L.B.1
St. John, P.L.2
Kovari, I.A.3
-
32
-
-
0344541695
-
Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney
-
H. Holthofer, H. Ahola, M.L. Solin Nephrin localizes at the podocyte filtration slit area and is characteristically spliced in the human kidney Am J Pathol 155 1999 1681 1687
-
(1999)
Am J Pathol
, vol.155
, pp. 1681-1687
-
-
Holthofer, H.1
Ahola, H.2
Solin, M.L.3
-
33
-
-
0033529312
-
Nephrin is specifically located at the slit diaphragm of glomerular podocytes
-
V. Ruotsalainen, P. Ljungberg, J. Wartiovaara Nephrin is specifically located at the slit diaphragm of glomerular podocytes Proc Natl Acad Sci U S A 96 1999 7962 7967
-
(1999)
Proc Natl Acad Sci U S a
, vol.96
, pp. 7962-7967
-
-
Ruotsalainen, V.1
Ljungberg, P.2
Wartiovaara, J.3
-
34
-
-
0035834659
-
Interaction with podocin facilitates nephrin signaling
-
T.B. Huber, M. Kottgen, B. Schilling Interaction with podocin facilitates nephrin signaling J Biol Chem 276 2001 41543 41546
-
(2001)
J Biol Chem
, vol.276
, pp. 41543-41546
-
-
Huber, T.B.1
Kottgen, M.2
Schilling, B.3
-
35
-
-
0034858027
-
Involvement of lipid rafts in nephrin phosphorylation and organization of the glomerular slit diaphragm
-
M. Simons, K. Schwarz, W. Kriz Involvement of lipid rafts in nephrin phosphorylation and organization of the glomerular slit diaphragm Am J Pathol 159 2001 1069 1077
-
(2001)
Am J Pathol
, vol.159
, pp. 1069-1077
-
-
Simons, M.1
Schwarz, K.2
Kriz, W.3
-
36
-
-
0037018760
-
Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations
-
J. Patrakka, P. Martin, R. Salonen Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations Lancet 359 2002 1575 1577
-
(2002)
Lancet
, vol.359
, pp. 1575-1577
-
-
Patrakka, J.1
Martin, P.2
Salonen, R.3
-
37
-
-
0037083989
-
Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: Role of nephrin
-
J. Patrakka, V. Ruotsalainen, P. Reponen Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type Role of nephrin Transplantation 73 2002 394 403
-
(2002)
Transplantation
, vol.73
, pp. 394-403
-
-
Patrakka, J.1
Ruotsalainen, V.2
Reponen, P.3
-
38
-
-
0034830940
-
Recurrence of nephrotic syndrome after transplantation in CNF is due to autoantibodies to nephrin
-
S.X. Wang, H. Ahola, T. Palmen Recurrence of nephrotic syndrome after transplantation in CNF is due to autoantibodies to nephrin Exp Nephrol 9 2001 327 331
-
(2001)
Exp Nephrol
, vol.9
, pp. 327-331
-
-
Wang, S.X.1
Ahola, H.2
Palmen, T.3
-
39
-
-
0035164681
-
The murine nephrin gene is specifically expressed in kidney, brain and pancreas: Inactivation of the gene leads to massive proteinuria and neonatal death
-
H. Putaala, R. Soininen, P. Kilpelainen The murine nephrin gene is specifically expressed in kidney, brain and pancreas Inactivation of the gene leads to massive proteinuria and neonatal death Hum Mol Genet 10 2001 1 8
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1-8
-
-
Putaala, H.1
Soininen, R.2
Kilpelainen, P.3
-
40
-
-
0033431774
-
Nephritogenic mAb 5-1-6 is directed at the extracellular domain of rat nephrin
-
P.S. Topham, K. Hiroshi, S.A. Haydar Nephritogenic mAb 5-1-6 is directed at the extracellular domain of rat nephrin J Clin Invest 104 1999 1559 1566
-
(1999)
J Clin Invest
, vol.104
, pp. 1559-1566
-
-
Topham, P.S.1
Hiroshi, K.2
Haydar, S.A.3
-
41
-
-
0036014942
-
Nephrin TRAP mice lack slit diaphragms and show fibrotic glomeruli and cystic tubular lesions
-
M. Rantanen, T. Palmén, A. Pätäri Nephrin TRAP mice lack slit diaphragms and show fibrotic glomeruli and cystic tubular lesions J Am Soc Nephrol 13 2002 1586 1594
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 1586-1594
-
-
Rantanen, M.1
Palmén, T.2
Pätäri, A.3
-
42
-
-
0028792063
-
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
-
A. Fuchshuber, G. Jean, O. Gribouval Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis Hum Mol Genet 4 1995 2155 2158
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2155-2158
-
-
Fuchshuber, A.1
Jean, G.2
Gribouval, O.3
-
43
-
-
0034034757
-
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
-
N. Boute, O. Gribouval, S. Roselli NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome Nat Genet 24 2000 349 354
-
(2000)
Nat Genet
, vol.24
, pp. 349-354
-
-
Boute, N.1
Gribouval, O.2
Roselli, S.3
-
44
-
-
0036144232
-
Podocin localizes in the kidney to the slit diaphragm area
-
S. Roselli, O. Gribouval, N. Boute Podocin localizes in the kidney to the slit diaphragm area Am J Pathol 160 2002 131 139
-
(2002)
Am J Pathol
, vol.160
, pp. 131-139
-
-
Roselli, S.1
Gribouval, O.2
Boute, N.3
-
45
-
-
0035210324
-
Podocin, a raft associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin
-
K. Schwarz, M. Simons, J. Reiser Podocin, a raft associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin J Clin Invest 108 2001 1621 1629
-
(2001)
J Clin Invest
, vol.108
, pp. 1621-1629
-
-
Schwarz, K.1
Simons, M.2
Reiser, J.3
-
46
-
-
0038136885
-
CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility
-
J. Kim, H. Wu, G. Green CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility Science 300 2003 1298 1300
-
(2003)
Science
, vol.300
, pp. 1298-1300
-
-
Kim, J.1
Wu, H.2
Green, G.3
-
47
-
-
3242795082
-
NPHS2 mutation analysis show genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
-
S. Weber, O. Gribouval, E.L. Esquivel NPHS2 mutation analysis show genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence Kidney Int 66 2004 571 579
-
(2004)
Kidney Int
, vol.66
, pp. 571-579
-
-
Weber, S.1
Gribouval, O.2
Esquivel, E.L.3
-
48
-
-
0032962032
-
Focal segmental glomerulosclerosis: A need for caution in live-related renal transplantation
-
M.P. Winn, A.M. Alkhunaizi, W.M. Bennett Focal segmental glomerulosclerosis a need for caution in live-related renal transplantation Am J Kidney Dis 33 1999 970 974
-
(1999)
Am J Kidney Dis
, vol.33
, pp. 970-974
-
-
Winn, M.P.1
Alkhunaizi, A.M.2
Bennett, W.M.3
-
49
-
-
0031884633
-
A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13
-
B.J. Mathis, S.H. Kim, K. Calabrese A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13 Kidney Int 53 1998 282 286
-
(1998)
Kidney Int
, vol.53
, pp. 282-286
-
-
Mathis, B.J.1
Kim, S.H.2
Calabrese, K.3
-
50
-
-
0034051681
-
Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis
-
J.M. Kaplan, S.H. Kim, K. North Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis Nat Genet 24 2001 251 256
-
(2001)
Nat Genet
, vol.24
, pp. 251-256
-
-
Kaplan, J.M.1
Kim, S.H.2
North, K.3
-
51
-
-
0038819061
-
Mice deficient in α-actinin-4 have severe glomerular disease
-
C.H. Kops, T.C. Le, S. Sunhat Mice deficient in α-actinin-4 have severe glomerular disease J Clin Invest 111 2003 1683 1690
-
(2003)
J Clin Invest
, vol.111
, pp. 1683-1690
-
-
Kops, C.H.1
Le, T.C.2
Sunhat, S.3
-
52
-
-
0033152045
-
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity
-
M.P. Winn, P.J. Conlon, K.L. Lynn Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity Genomics 58 1999 113 120
-
(1999)
Genomics
, vol.58
, pp. 113-120
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
53
-
-
20844461826
-
A mutation in the trpc6 cation channel causes familial focal segmental glomerulosclerosis
-
published online May 5 (doi:10.1125/science. 1106215)
-
Winn MP, Conlon PJ, Lynn KL,, et al. A mutation in the trpc6 cation channel causes familial focal segmental glomerulosclerosis. Science published online May 5 2005 (doi:10.1125/science. 1106215) Available at: http://www.sciencemag.org/, date accessed May 5, 2005
-
(2005)
Science
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
55
-
-
0033536599
-
Congenital nephrotic syndrome in mice lacking CD2-associated protein
-
N.Y. Shih, J. Li, V. Karpitskii Congenital nephrotic syndrome in mice lacking CD2-associated protein Science 286 1999 312 315
-
(1999)
Science
, vol.286
, pp. 312-315
-
-
Shih, N.Y.1
Li, J.2
Karpitskii, V.3
-
56
-
-
22844436647
-
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function
-
published online May 27 (doi:10.1038/ng1592)
-
Reiser J, Polu K, Möller C,, et al. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Nat Genet published online May 27 2005 (doi:10.1038/ng1592) Available at: http://www.nature.com/ng/index.html, date accessed May 27, 2005
-
(2005)
Nat Genet
-
-
Reiser, J.1
Polu, K.2
Möller, C.3
|