-
1
-
-
42149122041
-
Properties of the glomerular barrier and mechanisms of proteinuria
-
Haraldsson, B., Nyström, J. & Deen, W. M. Properties of the glomerular barrier and mechanisms of proteinuria. Physiol Rev. 88, 451-487 (2008).
-
(2008)
Physiol Rev.
, vol.88
, pp. 451-487
-
-
Haraldsson, B.1
Nyström, J.2
Deen, W.M.3
-
2
-
-
0037207471
-
Cell biology of the glomerular podocyte
-
Pavenstädt, H., Kriz, W. & Kretzler, M. Cell biology of the glomerular podocyte. Physiol. Rev. 83, 253-307 (2003).
-
(2003)
Physiol. Rev.
, vol.83
, pp. 253-307
-
-
Pavenstädt, H.1
Kriz, W.2
Kretzler, M.3
-
3
-
-
33645548140
-
Transgenic isolation of skeletal muscle and kidney defects in laminin β2 mutant mice: Implications for Pierson syndrome
-
Miner, J. H., Go, G., Cunningham, J., Patton, B. L. & Jarad, G. Transgenic isolation of skeletal muscle and kidney defects in laminin β2 mutant mice: Implications for Pierson syndrome. Development 133, 967-975 (2006).
-
(2006)
Development
, vol.133
, pp. 967-975
-
-
Miner, J.H.1
Go, G.2
Cunningham, J.3
Patton, B.L.4
Jarad, G.5
-
4
-
-
67649687035
-
Cellular origins of type IV collagen networks in developing glomeruli
-
Abrahamson, D. R., Hudson, B. G., Stroganova, L., Borza, D. B. & St John, P. L. Cellular origins of type IV collagen networks in developing glomeruli. J. Am. Soc. Nephrol. 20, 1471-1479 (2009).
-
(2009)
J. Am. Soc. Nephrol.
, vol.20
, pp. 1471-1479
-
-
Abrahamson, D.R.1
Hudson, B.G.2
Stroganova, L.3
Borza, D.B.4
St John, P.L.5
-
5
-
-
3242749316
-
The role of VEGF-A in glomerular development and function
-
Eremina, V. & Quaggin, S. E. The role of VEGF-A in glomerular development and function. Curr. Opin. Nephrol. Hypertens. 13, 9-15 (2004).
-
(2004)
Curr. Opin. Nephrol. Hypertens.
, vol.13
, pp. 9-15
-
-
Eremina, V.1
Quaggin, S.E.2
-
6
-
-
1542349097
-
Angiopoietin 1 and vascular endothelial growth factor modulate human glomerular endothelial cell barrier properties
-
Satchell, S. C., Anderson, K. L. & Mathieson, P. W. Angiopoietin 1 and vascular endothelial growth factor modulate human glomerular endothelial cell barrier properties. J. Am. Soc. Nephrol. 15, 566-574 (2004).
-
(2004)
J. Am. Soc. Nephrol.
, vol.15
, pp. 566-574
-
-
Satchell, S.C.1
Anderson, K.L.2
Mathieson, P.W.3
-
7
-
-
0036156877
-
Human podocytes express angiopoietin 1, a potential regulator of glomerular vascular endothelial growth factor
-
Satchell, S. C. et al. Human podocytes express angiopoietin 1, a potential regulator of glomerular vascular endothelial growth factor. J. Am. Soc. Nephrol. 13, 544-550 (2002).
-
(2002)
J. Am. Soc. Nephrol.
, vol.13
, pp. 544-550
-
-
Satchell, S.C.1
-
8
-
-
38949210805
-
Podocytes use FcRn to clear IgG from the glomerular basement membrane
-
Akilesh, S. et al. Podocytes use FcRn to clear IgG from the glomerular basement membrane. Proc. Natl Acad. Sci. USA 105, 967-972 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 967-972
-
-
Akilesh, S.1
-
9
-
-
0002965692
-
Glomerular permeability. I Ferritin transfer across the normal glomerular capillary wall
-
Farquhar, M. G., Wissig, S. L. & Palade, G. E. Glomerular permeability. I. Ferritin transfer across the normal glomerular capillary wall. J. Exp. Med. 113, 47-66 (1961).
-
(1961)
J. Exp. Med.
, vol.113
, pp. 47-66
-
-
Farquhar, M.G.1
Wissig, S.L.2
Palade, G.E.3
-
10
-
-
0010264078
-
Some features of glomerular filtration and permeability revealed by electron microscopy after intraperitoneal injection of dextran in rats
-
James, J. A. & Ashworth, C. T. Some features of glomerular filtration and permeability revealed by electron microscopy after intraperitoneal injection of dextran in rats. Am. J. Pathol. 38, 515-525 (1961).
-
(1961)
Am. J. Pathol.
, vol.38
, pp. 515-525
-
-
James, J.A.1
Ashworth, C.T.2
-
11
-
-
2542494061
-
Signaling at the slit diaphragm
-
Benzing, T. Signaling at the slit diaphragm. J. Am. Soc. Nephrol. 15, 1382-1391 (2004).
-
(2004)
J. Am. Soc. Nephrol.
, vol.15
, pp. 1382-1391
-
-
Benzing, T.1
-
12
-
-
18844411833
-
The slit diaphragm: A signaling platform to regulate podocyte function
-
Huber, T. B. & Benzing, T. The slit diaphragm: A signaling platform to regulate podocyte function. Curr. Opin. Nephrol. Hypertens. 14, 211-216 (2005).
-
(2005)
Curr. Opin. Nephrol. Hypertens.
, vol.14
, pp. 211-216
-
-
Huber, T.B.1
Benzing, T.2
-
13
-
-
2342509032
-
A podocentric view of nephrology
-
Ly, J., Alexander, M. & Quaggin, S. E. A podocentric view of nephrology. Curr. Opin. Nephrol. Hypertens. 13, 299-305 (2004).
-
(2004)
Curr. Opin. Nephrol. Hypertens.
, vol.13
, pp. 299-305
-
-
Ly, J.1
Alexander, M.2
Quaggin, S.E.3
-
14
-
-
0036891810
-
Podocyte biology and response to injury
-
Mundel, P. & Shankland, S. J. Podocyte biology and response to injury. J. Am. Soc. Nephrol. 13, 3005-3015 (2002).
-
(2002)
J. Am. Soc. Nephrol.
, vol.13
, pp. 3005-3015
-
-
Mundel, P.1
Shankland, S.J.2
-
15
-
-
0031706336
-
Progression of glomerular diseases: Is the podocyte the culprit?
-
Kriz, W., Gretz, N., & Lemley, K V. Progression of glomerular diseases: Is the podocyte the culprit? Kidney Int. 54, 687-697 (1998).
-
(1998)
Kidney Int.
, vol.54
, pp. 687-697
-
-
Kriz, W.1
Gretz, N.2
Lemley, K.V.3
-
16
-
-
0002965693
-
Glomerular permeability II. Ferritin transfer across the glomerular capillary wall in nephrotic rats
-
Farquhar, M. G. & Palade, G. E. Glomerular permeability. II. Ferritin transfer across the glomerular capillary wall in nephrotic rats. J. Exp. Med. 114, 699-716 (1961).
-
(1961)
J. Exp. Med.
, vol.114
, pp. 699-716
-
-
Farquhar, M.G.1
Palade, G.E.2
-
17
-
-
0016799620
-
The permeability of glomerular capillaries of aminonuceoside nephrotic rats to graded dextrans
-
Caulfield, J. P. & Farquhar, M. G. The permeability of glomerular capillaries of aminonuceoside nephrotic rats to graded dextrans. J. Exp. Med. 142, 61-83 (1975).
-
(1975)
J. Exp. Med.
, vol.142
, pp. 61-83
-
-
Caulfield, J.P.1
Farquhar, M.G.2
-
18
-
-
0015953201
-
Porous substructure of the glomerular slit diaphragm in the rat and mouse
-
Rodewald, R. & Karnovsky, M. J. Porous substructure of the glomerular slit diaphragm in the rat and mouse. J. Cell Biol. 60, 423-433 (1974).
-
(1974)
J. Cell Biol.
, vol.60
, pp. 423-433
-
-
Rodewald, R.1
Karnovsky, M.J.2
-
19
-
-
0016809348
-
An ultrastructural study of the mechanisms of proteinuria in aminonucleoside nephrosis
-
Ryan, G. B. & Karnovsky, M. J. An ultrastructural study of the mechanisms of proteinuria in aminonucleoside nephrosis. Kidney Int. 8, 219-232 (1975).
-
(1975)
Kidney Int.
, vol.8
, pp. 219-232
-
-
Ryan, G.B.1
Karnovsky, M.J.2
-
20
-
-
0026445848
-
Intrarenal handling of proteins in rats using fractional micropuncture technique
-
Tojo, A. & Endou, H. Intrarenal handling of proteins in rats using fractional micropuncture technique. Am. J. Physiol. 263, F601-F606 (1992).
-
(1992)
Am. J. Physiol.
, vol.263
-
-
Tojo, A.1
Endou, H.2
-
21
-
-
62149094328
-
Lipid-protein interactions along the slit diaphragm of podocytes
-
Schermer, B. & Benzing, T. Lipid-protein interactions along the slit diaphragm of podocytes. J. Am. Soc. Nephrol. 20, 473-478 (2009).
-
(2009)
J. Am. Soc. Nephrol.
, vol.20
, pp. 473-478
-
-
Schermer, B.1
Benzing, T.2
-
22
-
-
0032015551
-
Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome
-
Kestilä, M. et al. Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome. Mol. Cell 1, 575-582 (1998).
-
(1998)
Mol. Cell
, vol.1
, pp. 575-582
-
-
Kestilä, M.1
-
23
-
-
0032861101
-
Nephrin localizes to the slit pore of the glomerular epithelial cell
-
Holzman, L. B. et al. Nephrin localizes to the slit pore of the glomerular epithelial cell. Kidney Int. 56, 1481-1491 (1999).
-
(1999)
Kidney Int.
, vol.56
, pp. 1481-1491
-
-
Holzman, L.B.1
-
24
-
-
0033529312
-
Nephrin is specifically located at the slit diaphragm of glomerular podocytes
-
Ruotsalainen, V. et al. Nephrin is specifically located at the slit diaphragm of glomerular podocytes. Proc. Natl Acad. Sci. USA 96, 7962-7967 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 7962-7967
-
-
Ruotsalainen, V.1
-
25
-
-
0035834659
-
Interaction with podocin facilitates nephrin signaling
-
Huber, T. B., Kottgen, M., Schilling, B., Walz, G. & Benzing, T. Interaction with podocin facilitates nephrin signaling. J. Biol. Chem. 276, 41543-41546 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 41543-41546
-
-
Huber, T.B.1
Kottgen, M.2
Schilling, B.3
Walz, G.4
Benzing, T.5
-
26
-
-
0037379340
-
Homodimerization and heterodimerization of the glomerular podocyte proteins nephrin and NEPH1
-
Gerke, P., Huber, T. B., Sellin, L., Benzing, T. & Walz, G. Homodimerization and heterodimerization of the glomerular podocyte proteins nephrin and NEPH1. J. Am. Soc. Nephrol. 14, 918-926 (2003).
-
(2003)
J. Am. Soc. Nephrol.
, vol.14
, pp. 918-926
-
-
Gerke, P.1
Huber, T.B.2
Sellin, L.3
Benzing, T.4
Walz, G.5
-
27
-
-
0038788840
-
Nephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signaling
-
Huber, T. B. et al. Nephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signaling. Mol. Cell. Biol. 23, 4917-4928 (2003).
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 4917-4928
-
-
Huber, T.B.1
-
28
-
-
0037968548
-
The carboxyl terminus of Neph family members binds to the PDZ domain protein zonula occludens-1
-
Huber, T. B. et al. The carboxyl terminus of Neph family members binds to the PDZ domain protein zonula occludens-1. J. Biol. Chem. 278, 13417-13421 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 13417-13421
-
-
Huber, T.B.1
-
29
-
-
0346121526
-
Molecular basis of the functional podocin-nephrin complex: Mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains
-
Huber, T. B. et al. Molecular basis of the functional podocin-nephrin complex: Mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains. Hum. Mol. Genet. 12, 3397-3405 (2003).
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 3397-3405
-
-
Huber, T.B.1
-
30
-
-
0037743504
-
Fyn binds to and phosphorylates the kidney slit diaphragm component Nephrin
-
Verma, R. et al. Fyn binds to and phosphorylates the kidney slit diaphragm component Nephrin. J. Biol. Chem. 278, 20716-20723 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 20716-20723
-
-
Verma, R.1
-
31
-
-
33646401549
-
Nephrin ectodomain engagement results in Src kinase activation, nephrin phosphorylation, Nck recruitment, and actin polymerization
-
Verma, R. et al. Nephrin ectodomain engagement results in Src kinase activation, nephrin phosphorylation, Nck recruitment, and actin polymerization. J Clin. Invest. 116, 1346-1359 (2006).
-
(2006)
J Clin. Invest.
, vol.116
, pp. 1346-1359
-
-
Verma, R.1
-
32
-
-
33645746950
-
Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes
-
Jones, N. et al. Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes. Nature 440, 818-823 (2006).
-
(2006)
Nature
, vol.440
, pp. 818-823
-
-
Jones, N.1
-
33
-
-
0035210580
-
Caught flat-footed: Podocyte damage and the molecular bases of focal glomerulosclerosis
-
Kerjaschki, D. Caught flat-footed: Podocyte damage and the molecular bases of focal glomerulosclerosis. J. Clin. Invest. 108, 1583-1587 (2001).
-
(2001)
J. Clin. Invest.
, vol.108
, pp. 1583-1587
-
-
Kerjaschki, D.1
-
34
-
-
33646400903
-
Clinical impact of research on the podocyte slit diaphragm
-
Johnstone, D. B. & Holzman, L. B. Clinical impact of research on the podocyte slit diaphragm. Nat. Clin. Pract. Nephrol. 2, 271-282 (2006).
-
(2006)
Nat. Clin. Pract. Nephrol.
, vol.2
, pp. 271-282
-
-
Johnstone, D.B.1
Holzman, L.B.2
-
35
-
-
82655173711
-
Role for a Cindr-Arf6 axis in patterning emerging epithelia
-
Johnson, R. I., Sedgwick, A., D'Souza-Schorey, C. & Cagan, R. L. Role for a Cindr-Arf6 axis in patterning emerging epithelia. Mol. Biol. Cell 22, 4513-4526 (2011).
-
(2011)
Mol. Biol. Cell
, vol.22
, pp. 4513-4526
-
-
Johnson, R.I.1
Sedgwick, A.2
D'Souza-Schorey, C.3
Cagan, R.L.4
-
36
-
-
19944391600
-
Preferential adhesion mediated by hibris and roughest regulates morphogenesis and patterning in the Drosophila eye
-
Bao, S. & Cagan, R. Preferential adhesion mediated by hibris and roughest regulates morphogenesis and patterning in the Drosophila eye. Dev. Cell 8, 925-935 (2005).
-
(2005)
Dev. Cell
, vol.8
, pp. 925-935
-
-
Bao, S.1
Cagan, R.2
-
37
-
-
79961131498
-
The BAR domain protein PICK1 regulates cell recognition and morphogenesis by interacting with Neph proteins
-
Höhne, M. et al. The BAR domain protein PICK1 regulates cell recognition and morphogenesis by interacting with Neph proteins. Mol. Cell. Biol. 31, 3241-3251 (2011).
-
(2011)
Mol. Cell. Biol.
, vol.31
, pp. 3241-3251
-
-
Höhne, M.1
-
38
-
-
77956586329
-
Recognition of pre- and postsynaptic neurons via nephrin/NEPH1 homologs is a basis for the formation of the Drosophila retinotopic map
-
Sugie, A., Umetsu, D., Yasugi, T., Fischback, K. F. & Tabata, T. Recognition of pre- and postsynaptic neurons via nephrin/NEPH1 homologs is a basis for the formation of the Drosophila retinotopic map. Development 137, 3303-3313 (2010).
-
(2010)
Development
, vol.137
, pp. 3303-3313
-
-
Sugie, A.1
Umetsu, D.2
Yasugi, T.3
Fischback, K.F.4
Tabata, T.5
-
39
-
-
0027767583
-
The irregular chiasm C-roughest locus of Drosophila, which affects axonal projections and programmed cell death, encodes a novel immunoglobulin-like protein
-
Ramos, R. G. et al. The irregular chiasm C-roughest locus of Drosophila, which affects axonal projections and programmed cell death, encodes a novel immunoglobulin-like protein. Genes Dev. 7, 2533-2547 (1993).
-
(1993)
Genes Dev.
, vol.7
, pp. 2533-2547
-
-
Ramos, R.G.1
-
40
-
-
0035164748
-
Rst and its paralogue kirre act redundantly during embryonic muscle development in Drosophila
-
Strünkelnberg, M. et al. Rst and its paralogue kirre act redundantly during embryonic muscle development in Drosophila. Development 128, 4229-4239 (2001).
-
(2001)
Development
, vol.128
, pp. 4229-4239
-
-
Strünkelnberg, M.1
-
41
-
-
58249123367
-
The insect nephrocyte is a podocyte-like cell with a filtration slit diaphragm
-
Weavers, H. et al. The insect nephrocyte is a podocyte-like cell with a filtration slit diaphragm. Nature 457, 322-326 (2009).
-
(2009)
Nature
, vol.457
, pp. 322-326
-
-
Weavers, H.1
-
42
-
-
69649091814
-
Sns and Kirre, the Drosophila orthologs of Nephrin and Neph1, direct adhesion, fusion and formation of a slit diaphragm-like structure in insect nephrocytes
-
Zhuang, S. et al. Sns and Kirre, the Drosophila orthologs of Nephrin and Neph1, direct adhesion, fusion and formation of a slit diaphragm-like structure in insect nephrocytes. Development 136, 2335-2344 (2009).
-
(2009)
Development
, vol.136
, pp. 2335-2344
-
-
Zhuang, S.1
-
44
-
-
66449089617
-
The irre cell recognition module (IRM) proteins
-
Fischbach, K. F. et al. The irre cell recognition module (IRM) proteins. J. Neurogenet. 23, 48-67 (2009).
-
(2009)
J. Neurogenet.
, vol.23
, pp. 48-67
-
-
Fischbach, K.F.1
-
45
-
-
0032730875
-
Unraveling the mechanisms of glomerular ultrafiltration: Nephrin, a key component of the slit diaphragm
-
Tryggvason, K. Unraveling the mechanisms of glomerular ultrafiltration: Nephrin, a key component of the slit diaphragm. J. Am. Soc. Nephrol. 10, 2440-2445 (1999).
-
(1999)
J. Am. Soc. Nephrol.
, vol.10
, pp. 2440-2445
-
-
Tryggvason, K.1
-
46
-
-
36549030701
-
Evidence for restriction of fluid and solute movement across the glomerular capillary wall by the subpodocyte space
-
Salmon, A. H. et al. Evidence for restriction of fluid and solute movement across the glomerular capillary wall by the subpodocyte space. Am. J. Physiol. Renal. Physiol. 293: F1777-F1786 (2007).
-
(2007)
Am. J. Physiol. Renal. Physiol.
, vol.293
-
-
Salmon, A.H.1
-
47
-
-
0037389827
-
Why the kidney glomerulus does not clog: A gel permeation/diffusion hypothesis of renal function
-
Smithies, O. Why the kidney glomerulus does not clog: A gel permeation/diffusion hypothesis of renal function. Proc. Natl Acad. Sci. USA 100, 4108-4113 (2003).
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 4108-4113
-
-
Smithies, O.1
-
49
-
-
16644386452
-
Glomerular filtration of albumin: How small is the sieving coefficient?
-
Deen, W. M. & Lazzara, M. J. Glomerular filtration of albumin: How small is the sieving coefficient? Kidney Int. Suppl. S63-S64 (2004).
-
(2004)
Kidney Int. Suppl.
-
-
Deen, W.M.1
Lazzara, M.J.2
-
50
-
-
78649884695
-
Electrical forces determine glomerular permeability
-
Hausmann, R. et al. Electrical forces determine glomerular permeability. J. Am. Soc. Nephrol. 21, 2053-2058 (2010).
-
(2010)
J. Am. Soc. Nephrol.
, vol.21
, pp. 2053-2058
-
-
Hausmann, R.1
-
51
-
-
77950462459
-
Genetic kidney diseases
-
Hildebrandt, F. Genetic kidney diseases. Lancet 375, 1287-1295 (2010).
-
(2010)
Lancet
, vol.375
, pp. 1287-1295
-
-
Hildebrandt, F.1
-
52
-
-
77950515351
-
Genetics of nephrotic syndrome: Connecting molecular genetics to podocyte physiology
-
Machuca, E., Benoit, G. & Antignac, C. Genetics of nephrotic syndrome: Connecting molecular genetics to podocyte physiology. Hum. Mol. Genet. 18, R185-R194 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
-
-
Machuca, E.1
Benoit, G.2
Antignac, C.3
-
53
-
-
33645413836
-
The genetic basis of human glomerular disease
-
Moller, C. C., Pollak, M. R. & Reiser, J. The genetic basis of human glomerular disease. Adv. Chronic Kidney Dis. 13, 166-173 (2006).
-
(2006)
Adv. Chronic Kidney Dis.
, vol.13
, pp. 166-173
-
-
Moller, C.C.1
Pollak, M.R.2
Reiser, J.3
-
54
-
-
84855171766
-
INF2 mutations in Charcot Marie Tooth disease with glomerulopathy
-
Boyer, O. et al. INF2 mutations in Charcot Marie Tooth disease with glomerulopathy. N. Engl. J. Med. 365, 2377-2388 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 2377-2388
-
-
Boyer, O.1
-
55
-
-
73349132341
-
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
-
Brown, E. J. et al. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nat. Genet. 42, 72-76 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 72-76
-
-
Brown, E.J.1
-
56
-
-
79551656622
-
Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis
-
Boyer, O. et al. Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis. J. Am. Soc. Nephrol. 22, 239-245 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 239-245
-
-
Boyer, O.1
-
57
-
-
16944365351
-
Donor splice-site mutations in WT1 are responsible for Frasier syndrome
-
Barbaux, S. et al. Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat. Genet. 17, 467-470 (1997).
-
(1997)
Nat. Genet.
, vol.17
, pp. 467-470
-
-
Barbaux, S.1
-
58
-
-
0026094584
-
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
-
Pelletier, J. et al. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 67, 437-447 (1991).
-
(1991)
Cell
, vol.67
, pp. 437-447
-
-
Pelletier, J.1
-
59
-
-
0033624770
-
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis
-
Denamur, E. et al. WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis. Kidney Int. 57, 1868-1872 (2000).
-
(2000)
Kidney Int.
, vol.57
, pp. 1868-1872
-
-
Denamur, E.1
-
60
-
-
33751531864
-
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
-
Hinkes, B. et al. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nat. Genet. 38, 1397-1405 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 1397-1405
-
-
Hinkes, B.1
-
61
-
-
42949101458
-
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
-
Gbadegesin, R. et al. Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS). Nephrol. Dial. Transplant. 23, 1291-1297 (2008).
-
(2008)
Nephrol. Dial. Transplant.
, vol.23
, pp. 1291-1297
-
-
Gbadegesin, R.1
-
62
-
-
77954597034
-
Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome
-
Machuca, E. et al. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. J. Am. Soc. Nephrol. 21, 1209-1217 (2010).
-
(2010)
J. Am. Soc. Nephrol.
, vol.21
, pp. 1209-1217
-
-
Machuca, E.1
-
63
-
-
0034034757
-
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
-
Boute, N. et al. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat. Genet. 24, 349-354 (2000).
-
(2000)
Nat. Genet.
, vol.24
, pp. 349-354
-
-
Boute, N.1
-
64
-
-
79952318060
-
Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation
-
Jungraithmayr, T. C. et al. Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation. J. Am. Soc. Nephrol. 22, 579-585 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 579-585
-
-
Jungraithmayr, T.C.1
-
65
-
-
3242795082
-
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
-
Weber, S. et al. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. Kidney Int. 66, 571-579 (2004).
-
(2004)
Kidney Int.
, vol.66
, pp. 571-579
-
-
Weber, S.1
-
66
-
-
22844436647
-
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function
-
Reiser, J. et al. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Nat. Genet. 37, 739-744 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 739-744
-
-
Reiser, J.1
-
67
-
-
20844461826
-
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
-
Winn, M. P. et al. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science 308, 1801-1804 (2005).
-
(2005)
Science
, vol.308
, pp. 1801-1804
-
-
Winn, M.P.1
-
68
-
-
0034051681
-
Mutations in ACTN4, encoding α actinin 4, cause familial focal segmental glomerulosclerosis
-
Kaplan, J. M. et al. Mutations in ACTN4, encoding α actinin 4, cause familial focal segmental glomerulosclerosis. Nat. Genet. 24, 251-256 (2000).
-
(2000)
Nat. Genet.
, vol.24
, pp. 251-256
-
-
Kaplan, J.M.1
-
69
-
-
0036144232
-
Podocin localizes in the kidney to the slit diaphragm area
-
Roselli, S. et al. Podocin localizes in the kidney to the slit diaphragm area. Am. J. Pathol. 160, 131-139 (2002).
-
(2002)
Am. J. Pathol.
, vol.160
, pp. 131-139
-
-
Roselli, S.1
-
70
-
-
34447136072
-
Podocin organizes ion channel-lipid supercomplexes: Implications for mechanosensation at the slit diaphragm
-
Huber, T. B., Schermer, B. & Benzing, T. Podocin organizes ion channel-lipid supercomplexes: Implications for mechanosensation at the slit diaphragm. Nephron Exp. Nephrol. 106, e27-e31 (2007).
-
(2007)
Nephron Exp. Nephrol.
, vol.106
-
-
Huber, T.B.1
Schermer, B.2
Benzing, T.3
-
71
-
-
33751225687
-
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels
-
Huber, T. B. et al. Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels. Proc. Natl Acad. Sci. USA 103, 17079-17086 (2006).
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 17079-17086
-
-
Huber, T.B.1
-
72
-
-
0037186523
-
MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation
-
Goodman, M. B. et al. MEC-2 regulates C. elegans DEG/ENaC channels needed for mechanosensation. Nature 415, 1039-1042 (2002).
-
(2002)
Nature
, vol.415
, pp. 1039-1042
-
-
Goodman, M.B.1
-
73
-
-
0028839194
-
A stomatin-like protein necessary for mechanosensation in C. elegans
-
Huang, M., Gu, G., Ferguson, E. L. & Chalfie, M. A stomatin-like protein necessary for mechanosensation in C. elegans. Nature 378, 292-295 (1995).
-
(1995)
Nature
, vol.378
, pp. 292-295
-
-
Huang, M.1
Gu, G.2
Ferguson, E.L.3
Chalfie, M.4
-
74
-
-
33646406847
-
Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP Fyn, and synaptopodin
-
Huber, T. B. et al. Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin. J. Clin. Invest. 116, 1337-1345 (2006).
-
(2006)
J. Clin. Invest.
, vol.116
, pp. 1337-1345
-
-
Huber, T.B.1
-
75
-
-
77957984504
-
TRPC6 channels and their binding partners in podocytes: Role in glomerular filtration and pathophysiology
-
Dryer, S. E. & Reiser, J. TRPC6 channels and their binding partners in podocytes: Role in glomerular filtration and pathophysiology. Am. J. Physiol. Renal Physiol. 299, F689-F701 (2010).
-
(2010)
Am. J. Physiol. Renal Physiol.
, vol.299
-
-
Dryer, S.E.1
Reiser, J.2
-
76
-
-
33745058119
-
The podocyte's response to injury: Role in proteinuria and glomerulosclerosis
-
Shankland, S. J. The podocyte's response to injury: Role in proteinuria and glomerulosclerosis. Kidney Int. 69, 2131-2147 (2006).
-
(2006)
Kidney Int.
, vol.69
, pp. 2131-2147
-
-
Shankland, S.J.1
-
77
-
-
84874040904
-
The podocyte's response to stress: The enigma of foot process effacement
-
Kriz, W., Shirato, I., Nagata, M., Lehir, M. & Lemley, K. V. The podocyte's response to stress: The enigma of foot process effacement. Am. J. Physiol. Renal Physiol. 304, F333-F347 (2012).
-
(2012)
Am. J. Physiol. Renal Physiol.
, vol.304
-
-
Kriz, W.1
Shirato, I.2
Nagata, M.3
Lehir, M.4
Lemley, K.V.5
-
78
-
-
78651252297
-
Podocyte-secreted angiopoietin like 4 mediates proteinuria in glucocorticoid-sensitive nephrotic syndrome
-
Clement, L. C. et al. Podocyte-secreted angiopoietin like 4 mediates proteinuria in glucocorticoid-sensitive nephrotic syndrome. Nat. Med. 17, 117-122 (2011).
-
(2011)
Nat. Med.
, vol.17
, pp. 117-122
-
-
Clement, L.C.1
-
79
-
-
84867519785
-
Soluble FLT1 binds lipid microdomains in podocytes to control cell morphology and glomerular barrier function
-
Jin, J. et al. Soluble FLT1 binds lipid microdomains in podocytes to control cell morphology and glomerular barrier function. Cell 151, 384-399 (2012).
-
(2012)
Cell
, vol.151
, pp. 384-399
-
-
Jin, J.1
-
80
-
-
79961132981
-
Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis
-
Wei, C. et al. Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis. Nat. Med. 17, 952-960 (2011).
-
(2011)
Nat. Med.
, vol.17
, pp. 952-960
-
-
Wei, C.1
-
81
-
-
33645456580
-
Vascular endothelial growth factor a signaling in the podocyte-endothelial compartment is required for mesangial cell migration and survival
-
Eremina, V. et al. Vascular endothelial growth factor a signaling in the podocyte-endothelial compartment is required for mesangial cell migration and survival. J. Am. Soc. Nephrol. 17, 724-735 (2006).
-
(2006)
J. Am. Soc. Nephrol.
, vol.17
, pp. 724-735
-
-
Eremina, V.1
-
82
-
-
40849130173
-
VEGF inhibition and renal thrombotic microangiopathy
-
Eremina, V. et al. VEGF inhibition and renal thrombotic microangiopathy. N. Engl. J. Med. 358, 1129-1136 (2008).
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 1129-1136
-
-
Eremina, V.1
-
83
-
-
10744227199
-
Circulating angiogenic factors and the risk of preeclampsia
-
Levine, R. J. et al. Circulating angiogenic factors and the risk of preeclampsia. N. Engl. J. Med. 350, 672-683 (2004).
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 672-683
-
-
Levine, R.J.1
-
84
-
-
80052149662
-
Pilot study of extracorporeal removal of soluble fms-like tyrosine kinase 1 in preeclampsia
-
Thadhani, R. et al. Pilot study of extracorporeal removal of soluble fms-like tyrosine kinase 1 in preeclampsia. Circulation 124, 940-950 (2011).
-
(2011)
Circulation
, vol.124
, pp. 940-950
-
-
Thadhani, R.1
-
85
-
-
51349162919
-
The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A
-
Faul, C. et al. The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A. Nat. Med. 14, 931-938 (2008).
-
(2008)
Nat. Med.
, vol.14
, pp. 931-938
-
-
Faul, C.1
-
86
-
-
79951617575
-
Over-expressing transient receptor potential cation channel 6 in podocytes induces cytoskeleton rearrangement through increases of intracellular Ca2+ and RhoA activation
-
Jiang, L. et al. Over-expressing transient receptor potential cation channel 6 in podocytes induces cytoskeleton rearrangement through increases of intracellular Ca2+ and RhoA activation. Exp. Biol. Med. (Maywood) 236, 184-193 (2011).
-
(2011)
Exp. Biol. Med. (Maywood)
, vol.236
, pp. 184-193
-
-
Jiang, L.1
-
87
-
-
78049524253
-
Antagonistic regulation of actin dynamics and cell motility by TRPC5 and TRPC6 channels
-
Tian, D. et al. Antagonistic regulation of actin dynamics and cell motility by TRPC5 and TRPC6 channels. Sci. Signal. 3, ra77 (2010).
-
(2010)
Sci. Signal.
, vol.3
-
-
Tian, D.1
-
88
-
-
34848907421
-
Actin up: Regulation of podocyte structure and function by components of the actin cytoskeleton
-
Faul, C., Asanuma, K., Yanagida-Asanuma, E., Kim, K. & Mundel, P. Actin up: Regulation of podocyte structure and function by components of the actin cytoskeleton. Trends Cell Biol. 17, 428-437 (2007).
-
(2007)
Trends Cell Biol.
, vol.17
, pp. 428-437
-
-
Faul, C.1
Asanuma, K.2
Yanagida-Asanuma, E.3
Kim, K.4
Mundel, P.5
-
89
-
-
57349168398
-
Modification of mineralocorticoid receptor function by Rac1 GTPase: Implication in proteinuric kidney disease
-
Shibata, S. et al. Modification of mineralocorticoid receptor function by Rac1 GTPase: Implication in proteinuric kidney disease. Nat. Med. 14, 1370-1376 (2008).
-
(2008)
Nat. Med.
, vol.14
, pp. 1370-1376
-
-
Shibata, S.1
-
90
-
-
84863534353
-
Podocyte-specific loss of Cdc42 leads to congenital nephropathy
-
Scott, R. P. et al. Podocyte-specific loss of Cdc42 leads to congenital nephropathy. J. Am. Soc. Nephrol. 23, 1149-1154 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 1149-1154
-
-
Scott, R.P.1
-
91
-
-
84862777971
-
Mechanisms of the proteinuria induced by Rho GTPases
-
Wang, L. et al. Mechanisms of the proteinuria induced by Rho GTPases. Kidney Int. 81, 1075-1085 (2012).
-
(2012)
Kidney Int.
, vol.81
, pp. 1075-1085
-
-
Wang, L.1
-
92
-
-
80052333245
-
Activation of RhoA in podocytes induces focal segmental glomerulosclerosis
-
Zhu, L., Jiang, R., Aoudjit, L., Jones, N. & Takano, T. Activation of RhoA in podocytes induces focal segmental glomerulosclerosis. J. Am. Soc. Nephrol. 22, 1621-1630 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 1621-1630
-
-
Zhu, L.1
Jiang, R.2
Aoudjit, L.3
Jones, N.4
Takano, T.5
-
93
-
-
84859778293
-
MTOR signaling in growth control and disease
-
Laplante, M. & Sabatini, D. M. mTOR signaling in growth control and disease. Cell 149, 274-293 (2012).
-
(2012)
Cell
, vol.149
, pp. 274-293
-
-
Laplante, M.1
Sabatini, D.M.2
-
94
-
-
84863230126
-
Inhibition of MTOR disrupts autophagic flux in podocytes
-
Ciná, D. P. et al. Inhibition of MTOR disrupts autophagic flux in podocytes. J. Am. Soc. Nephrol. 23, 412-420 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 412-420
-
-
Ciná, D.P.1
-
95
-
-
40649124774
-
MToR inhibitors-induced proteinuria: Mechanisms, significance, and management
-
Letavernier, E. & Legendre, C. mToR inhibitors-induced proteinuria: Mechanisms, significance, and management. Transplant. Rev. (Orlando) 22, 125-130 (2008).
-
(2008)
Transplant. Rev. (Orlando)
, vol.22
, pp. 125-130
-
-
Letavernier, E.1
Legendre, C.2
-
96
-
-
79957927211
-
MTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in mice
-
Inoki, K. et al. mTORC1 activation in podocytes is a critical step in the development of diabetic nephropathy in mice. J. Clin. Invest. 121, 2181-2196 (2011).
-
(2011)
J. Clin. Invest.
, vol.121
, pp. 2181-2196
-
-
Inoki, K.1
-
97
-
-
79957881425
-
Role of mTOR in podocyte function and diabetic nephropathy in humans and mice
-
Gödel, M. et al. Role of mTOR in podocyte function and diabetic nephropathy in humans and mice. J. Clin. Invest. 121, 2197-2209 (2011).
-
(2011)
J. Clin. Invest.
, vol.121
, pp. 2197-2209
-
-
Gödel, M.1
-
98
-
-
84869191932
-
Intrinsic proinflammatory signaling in podocytes contributes to podocyte damage and prolonged proteinuria
-
Brahler, S. et al. Intrinsic proinflammatory signaling in podocytes contributes to podocyte damage and prolonged proteinuria. Am. J. Physiol. Renal. Physiol. 303, F1473-F1485 (2012).
-
(2012)
Am. J. Physiol. Renal. Physiol.
, vol.303
-
-
Brahler, S.1
-
99
-
-
57349158456
-
Proteinuria and immunityan overstated relationship? N
-
Mathieson, P. W. Proteinuria and immunity - an overstated relationship? N. Engl. J. Med. 359, 2492-2494 (2008).
-
(2008)
Engl. J. Med.
, vol.359
, pp. 2492-2494
-
-
Mathieson, P.W.1
-
100
-
-
68049120573
-
Nephrin deficiency activates NF-κB and promotes glomerular injury
-
Hussain, S. et al. Nephrin deficiency activates NF-κB and promotes glomerular injury. J. Am. Soc. Nephrol. 20, 1733-1743 (2009).
-
(2009)
J. Am. Soc. Nephrol.
, vol.20
, pp. 1733-1743
-
-
Hussain, S.1
-
101
-
-
84859838187
-
Podocytes: Gaining a foothold
-
Garg, P. & Holzman, L. B. Podocytes: Gaining a foothold. Exp. Cell Res. 318, 955-963 (2012).
-
(2012)
Exp. Cell Res.
, vol.318
, pp. 955-963
-
-
Garg, P.1
Holzman, L.B.2
-
102
-
-
58449096160
-
An essential role of the universal polarity protein, aPKCλ, on the maintenance of podocyte slit diaphragms
-
Hirose, T. et al. An essential role of the universal polarity protein, aPKCλ, on the maintenance of podocyte slit diaphragms. PLoS ONE 4, e4194 (2009).
-
(2009)
PLoS ONE
, vol.4
-
-
Hirose, T.1
-
103
-
-
65249087940
-
Loss of podocyte aPKCλ/ι causes polarity defects and nephrotic syndrome
-
Huber, T. B. et al. Loss of podocyte aPKCλ/ι causes polarity defects and nephrotic syndrome. J. Am. Soc. Nephrol. 20, 798-806 (2009).
-
(2009)
J. Am. Soc. Nephrol.
, vol.20
, pp. 798-806
-
-
Huber, T.B.1
-
104
-
-
84860610274
-
Role of the polarity protein Scribble for podocyte differentiation and maintenance
-
Hartleben, B. et al. Role of the polarity protein Scribble for podocyte differentiation and maintenance. PLoS ONE 7, e36705 (2012).
-
(2012)
Plos One
, vol.7
-
-
Hartleben, B.1
-
105
-
-
53149104790
-
Neph-Nephrin proteins bind the Par3-Par6-atypical protein kinase C (aPKC) complex to regulate podocyte cell polarity
-
Hartleben, B. et al. Neph-Nephrin proteins bind the Par3-Par6-atypical protein kinase C (aPKC) complex to regulate podocyte cell polarity. J. Biol. Chem. 283, 23033-23038 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 23033-23038
-
-
Hartleben, B.1
-
106
-
-
70349971175
-
Cyclin I activates Cdk5 and regulates expression of Bcl-2 and Bcl-XL in postmitotic mouse cells
-
Brinkkoetter, P. T. et al. Cyclin I activates Cdk5 and regulates expression of Bcl-2 and Bcl-XL in postmitotic mouse cells. J. Clin. Invest. 119, 3089-3101 (2009).
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 3089-3101
-
-
Brinkkoetter, P.T.1
-
107
-
-
77950518143
-
P35, the non-cyclin activator of Cdk5, protects podocytes against apoptosis in vitro and in vivo
-
Brinkkoetter, P. T. et al. p35, the non-cyclin activator of Cdk5, protects podocytes against apoptosis in vitro and in vivo. Kidney Int. 77, 690-699 (2010).
-
(2010)
Kidney Int.
, vol.77
, pp. 690-699
-
-
Brinkkoetter, P.T.1
-
108
-
-
33644783770
-
Glucose-induced reactive oxygen species cause apoptosis of podocytes and podocyte depletion at the onset of diabetic nephropathy
-
Susztak, K., Raff, A. C., Schiffer, M. & Böttinger, E. P. Glucose-induced reactive oxygen species cause apoptosis of podocytes and podocyte depletion at the onset of diabetic nephropathy. Diabetes 55, 225-233 (2006).
-
(2006)
Diabetes
, vol.55
, pp. 225-233
-
-
Susztak, K.1
Raff, A.C.2
Schiffer, M.3
Böttinger, E.P.4
-
109
-
-
0034836835
-
Apoptosis in podocytes induced by TGF-β and Smad7
-
Schiffer, M. et al. Apoptosis in podocytes induced by TGF-β and Smad7. J. Clin. Invest. 108, 807-816 (2001).
-
(2001)
J. Clin. Invest.
, vol.108
, pp. 807-816
-
-
Schiffer, M.1
-
110
-
-
29144490392
-
Podocyte depletion causes glomerulosclerosis: Diphtheria toxin-induced podocyte depletion in rats expressing human diphtheria toxin receptor transgene
-
Wharram, B. L. et al. Podocyte depletion causes glomerulosclerosis: Diphtheria toxin-induced podocyte depletion in rats expressing human diphtheria toxin receptor transgene. J. Am. Soc. Nephrol. 16, 2941-2952 (2005).
-
(2005)
J. Am. Soc. Nephrol.
, vol.16
, pp. 2941-2952
-
-
Wharram, B.L.1
-
111
-
-
44949105375
-
Cyclin-dependent kinase 5 supports neuronal survival through phosphorylation of Bcl-2
-
Cheung, Z. H., Gong, K. & Ip, N. Y. Cyclin-dependent kinase 5 supports neuronal survival through phosphorylation of Bcl-2. J. Neurosci. 28, 4872-4877 (2008).
-
(2008)
J. Neurosci.
, vol.28
, pp. 4872-4877
-
-
Cheung, Z.H.1
Gong, K.2
Ip, N.Y.3
-
112
-
-
84925940808
-
Pathology of human diabetic nephropathy
-
Najafian, B., Alpers, C. E. & Fogo, A. B. Pathology of human diabetic nephropathy. Contrib. Nephrol. 170, 36-47 (2011).
-
(2011)
Contrib. Nephrol.
, vol.170
, pp. 36-47
-
-
Najafian, B.1
Alpers, C.E.2
Fogo, A.B.3
-
113
-
-
34548860393
-
Cumulative excretion of urinary podocytes reflects disease progression in IgA nephropathy and Schönlein-Henoch purpura nephritis
-
Hara, M., Yanagihara, T. & Kihara, I. Cumulative excretion of urinary podocytes reflects disease progression in IgA nephropathy and Schönlein-Henoch purpura nephritis. Clin. J. Am. Soc. Nephrol. 2, 231-238 (2007).
-
(2007)
Clin. J. Am. Soc. Nephrol.
, vol.2
, pp. 231-238
-
-
Hara, M.1
Yanagihara, T.2
Kihara, I.3
-
114
-
-
84872744396
-
Light microscopic visualization of podocyte ultrastructure demonstrates oscillating glomerular contractions
-
Höhne, M. et al. Light microscopic visualization of podocyte ultrastructure demonstrates oscillating glomerular contractions. Am. J. Pathol. 182, 332-338 (2012).
-
(2012)
Am. J. Pathol.
, vol.182
, pp. 332-338
-
-
Höhne, M.1
-
115
-
-
84860606114
-
Imaging of podocyte foot processes by fluorescence microscopy
-
Grgic, I. et al. Imaging of podocyte foot processes by fluorescence microscopy. J. Am. Soc. Nephrol. 23, 785-791 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 785-791
-
-
Grgic, I.1
-
116
-
-
78149355567
-
A high-powered view of the filtration barrier
-
Peti-Peterdi, J. & Sipos, A. A high-powered view of the filtration barrier. J. Am. Soc. Nephrol. 21, 1835-1841 (2010).
-
(2010)
J. Am. Soc. Nephrol.
, vol.21
, pp. 1835-1841
-
-
Peti-Peterdi, J.1
Sipos, A.2
-
117
-
-
84855323656
-
The first decade of using multiphoton microscopy for high-power kidney imaging
-
Peti-Peterdi, J., Burford, J. L. & Hackl, M. J. The first decade of using multiphoton microscopy for high-power kidney imaging. Am. J. Physiol. Renal Physiol. 302, F227-F233 (2012).
-
(2012)
Am. J. Physiol. Renal Physiol.
, vol.302
-
-
Peti-Peterdi, J.1
Burford, J.L.2
Hackl, M.J.3
-
118
-
-
84868626379
-
Multiphoton imaging of the glomerular permeability of angiotensinogen
-
Nakano, D. et al. Multiphoton imaging of the glomerular permeability of angiotensinogen. J. Am. Soc. Nephrol. 23, 1847-1856 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 1847-1856
-
-
Nakano, D.1
-
119
-
-
80555134774
-
Fishing for new glomerular disease-related genes
-
Mangos, S. & Reiser, J. Fishing for new glomerular disease-related genes. J. Am. Soc. Nephrol. 22, 1960-1962 (2011).
-
(2011)
J. Am. Soc. Nephrol.
, vol.22
, pp. 1960-1962
-
-
Mangos, S.1
Reiser, J.2
-
120
-
-
84455208254
-
The podocyte as a target for therapiesnew and old
-
Mathieson, P. W. The podocyte as a target for therapies - new and old. Nat. Rev. Nephrol. 8, 52-56 (2012).
-
(2012)
Nat. Rev. Nephrol.
, vol.8
, pp. 52-56
-
-
Mathieson, P.W.1
-
121
-
-
84861801845
-
A photo shoot of proteinuria: Zebrafish models of inducible podocyte damage
-
Muller, R. U. & Benzing, T. A photo shoot of proteinuria: Zebrafish models of inducible podocyte damage. J. Am. Soc. Nephrol. 23, 969-971 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 969-971
-
-
Muller, R.U.1
Benzing, T.2
-
122
-
-
25844519579
-
Organization of the pronephric filtration apparatus in zebrafish requires nephrin podocin and the ferm domain protein mosaic eyes
-
Kramer-Zucker, A. G., Wiessner, S., Jensen, A. M. & Drummond, I. A. Organization of the pronephric filtration apparatus in zebrafish requires Nephrin, Podocin and the FERM domain protein Mosaic eyes. Dev. Biol. 285, 316-329 (2005).
-
(2005)
Dev. Biol.
, vol.285
, pp. 316-329
-
-
Kramer-Zucker, A.G.1
Wiessner, S.2
Jensen, A.M.3
Drummond, I.A.4
-
123
-
-
36048976375
-
Rapid screening of glomerular slit diaphragm integrity in larval zebrafish
-
Hentschel, D. M. et al. Rapid screening of glomerular slit diaphragm integrity in larval zebrafish. Am. J. Physiol. Renal Physiol. 293, F1746-F1750 (2007).
-
(2007)
Am. J. Physiol. Renal Physiol.
, vol.293
-
-
Hentschel, D.M.1
-
124
-
-
84861799316
-
Inducible podocyte injury and proteinuria in transgenic zebrafish
-
Zhou, W. & Hildebrandt, F. Inducible podocyte injury and proteinuria in transgenic zebrafish. J. Am. Soc. Nephrol. 23, 1039-1047 (2012).
-
(2012)
J. Am. Soc. Nephrol.
, vol.23
, pp. 1039-1047
-
-
Zhou, W.1
Hildebrandt, F.2
-
125
-
-
0038136885
-
CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility
-
Kim, J. M. et al. CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. Science 23, 1298-1300 (2003).
-
(2003)
Science
, vol.23
, pp. 1298-1300
-
-
Kim, J.M.1
-
126
-
-
8444221929
-
Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and disinct eye abnormalities
-
Zenker, M. et al. Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and disinct eye abnormalities. Hum. Mol. Genet. 13, 2625-2632 (2004).
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2625-2632
-
-
Zenker, M.1
-
127
-
-
79960877647
-
MYO1E mutations and childhood familial focal segmenal glomerulosclerosis
-
Mele, C. et al. MYO1E mutations and childhood familial focal segmenal glomerulosclerosis. N. Engl. J. Med. 365, 295-306 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 295-306
-
-
Mele, C.1
-
128
-
-
79955520308
-
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
-
Heeringa, S. F. et al. COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. J. Clin. Invest. 121, 2013-2024 (2011).
-
(2011)
J. Clin. Invest.
, vol.121
, pp. 2013-2024
-
-
Heeringa, S.F.1
-
129
-
-
80051544854
-
Disruption of PTPRO causes childhood-onset nephrotic syndrome
-
Ozaltin, F. et al. Disruption of PTPRO causes childhood-onset nephrotic syndrome. Am. J. Hum. Genet. 89, 139-147 (2011).
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 139-147
-
-
Ozaltin, F.1
-
130
-
-
0022357227
-
The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): A distinctive glomerular lesionreport of 10 cases
-
Habib, R. et al. The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): A distinctive glomerular lesion - report of 10 cases. Clin. Nephrol. 24, 269-278 (1985).
-
(1985)
Clin. Nephrol.
, vol.24
, pp. 269-278
-
-
Habib, R.1
-
131
-
-
0033812573
-
Mutations in MYH9 result in the May-Hegglin anomaly, and Fectner and Sebastian Syndromes
-
Seri, M. et al. Mutations in MYH9 result in the May-Hegglin anomaly, and Fectner and Sebastian Syndromes. Nat. Genet. 26, 103-105 (2000).
-
(2000)
Nat. Genet.
, vol.26
, pp. 103-105
-
-
Seri, M.1
-
132
-
-
0031800728
-
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
-
Dreyer, S. D. et al. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome. Nat. Genet. 19, 47-50 (1998).
-
(1998)
Nat. Genet.
, vol.19
, pp. 47-50
-
-
Dreyer, S.D.1
-
133
-
-
0032471924
-
Mutation analysis of LMX1B gene in nail patella syndrome patients
-
McIntosh, I. et al. Mutation analysis of LMX1B gene in nail patella syndrome patients. Am. J. Hum. Genet. 63, 1651-1658 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1651-1658
-
-
McIntosh, I.1
-
134
-
-
0031750061
-
Loss of function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome
-
Vollrath, D. et al. Loss of function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome. Hum. Mol. Genet. 7, 1091-1098 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1091-1098
-
-
Vollrath, D.1
-
135
-
-
18544381908
-
Mutant chromatin remodelling protein SMARCAL1 causes Schimke immuno-osseous dysplasia
-
Boerkoel, C. F. et al., Mutant chromatin remodelling protein SMARCAL1 causes Schimke immuno-osseous dysplasia. Nat. Genet. 30, 215-220 (2002).
-
(2002)
Nat. Genet.
, vol.30
, pp. 215-220
-
-
Boerkoel, C.F.1
-
136
-
-
31544480133
-
A mutation in para hydroxybenzoate polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency
-
Quinzii, C. et al. A mutation in para hydroxybenzoate polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency. Am. J. Hum. Genet. 78, 345-349 (2006).
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 345-349
-
-
Quinzii, C.1
-
137
-
-
23844469463
-
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: A CoQ10-responsive condition
-
Salviati, L. et al. Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: A CoQ10-responsive condition. Neurology 65, 606-608 (2005).
-
(2005)
Neurology
, vol.65
, pp. 606-608
-
-
Salviati, L.1
-
138
-
-
33845232634
-
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl disphosphate synthase subunit 2 (PDSS2) mutations
-
López, L. C. et al. Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl disphosphate synthase subunit 2 (PDSS2) mutations. Am. J. Hum. Genet. 79, 1125-1129 (2006).
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 1125-1129
-
-
López, L.C.1
-
139
-
-
0031774828
-
A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation
-
Kurogouchi, F. et al. A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation. Am. J. Nephrol. 18, 551-556 (1998).
-
(1998)
Am. J. Nephrol.
, vol.18
, pp. 551-556
-
-
Kurogouchi, F.1
-
140
-
-
0025666322
-
A mutation in the tRNALeu(URR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
Goto, Y., Nonaka, I. & Horai, S. A mutation in the tRNALeu(URR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature, 348, 651-653 (1990).
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
141
-
-
46249129691
-
A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome
-
Balreira, A. et al. A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. Hum. Mol. Genet. 17, 2238-2243 (2008).
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2238-2243
-
-
Balreira, A.1
-
142
-
-
40849144062
-
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis
-
Berkovic, S. F. et al. Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis. Am. J. Hum. Genet. 82, 673-684 (2008).
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 673-684
-
-
Berkovic, S.F.1
-
143
-
-
40649121075
-
Mutations in FN1 cause glomerulopathy with fibronectin deposits
-
Castelletti, F. et al. Mutations in FN1 cause glomerulopathy with fibronectin deposits. Proc.Natl. Acad. Sci. USA 105, 2538-2543 (2008).
-
(2008)
Proc.Natl. Acad. Sci. USA
, vol.105
, pp. 2538-2543
-
-
Castelletti, F.1
|