-
1
-
-
0042466540
-
Nephrotic syndrome in childhood
-
Eddy AA, Symons JM. Nephrotic syndrome in childhood. Lancet 2003; 362: 629-639
-
(2003)
Lancet
, vol.362
, pp. 629-639
-
-
Eddy, A.A.1
Symons, J.M.2
-
2
-
-
0034034757
-
NPHS2, Encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
-
Erratum in Nat Genet. 2000;25:125
-
Boute N, Gribouval O, Roselli S et al. NPHS2, Encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet 2000; 24: 349-354. Erratum in Nat Genet. 2000;25:125
-
(2000)
Nat Genet
, vol.24
, pp. 349-354
-
-
Boute, N.1
Gribouval, O.2
Roselli, S.3
-
3
-
-
0034051681
-
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
-
Kaplan JM, Kim SH, North KN et al. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. 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
-
4
-
-
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
-
5
-
-
33751531864
-
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
-
Hinkes B,Wiggins RC, Gbadegesin R et al. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nat Genet 2006; 38: 1397-1405
-
(2006)
Nat Genet
, vol.38
, pp. 1397-1405
-
-
Hinkes, B.1
Wiggins, R.C.2
Gbadegesin, R.3
-
6
-
-
52949110955
-
MYH9 Is a major-effect risk gene for focal segmental glomerulosclerosis
-
Kopp JB, Smith MW, Nelson GW et al. MYH9 Is a major-effect risk gene for focal segmental glomerulosclerosis. Nat Genet 2008; 40: 1175-1184
-
(2008)
Nat Genet
, vol.40
, pp. 1175-1184
-
-
Kopp, J.B.1
Smith, M.W.2
Nelson, G.W.3
-
7
-
-
52949092735
-
Family investigation of nephropathy and diabetes research group: MYH9 is associated with nondiabetic end-stage renal disease in African Americans
-
Kao WH, Klag MJ, Meoni LA et al. Family investigation of nephropathy and diabetes research group: MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nat Genet 2008; 40: 1185-1192
-
(2008)
Nat Genet
, vol.40
, pp. 1185-1192
-
-
Kao, W.H.1
Klag, M.J.2
Meoni, L.A.3
-
8
-
-
77955646179
-
Association of trypanolytic ApoL1 variants with kidney disease in African Americans
-
Genovese G, Friedman DJ, Ross MD et al. Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science 2010; 329: 841-845
-
(2010)
Science
, vol.329
, pp. 841-845
-
-
Genovese, G.1
Friedman, D.J.2
Ross, M.D.3
-
9
-
-
80555148891
-
Population-based risk assessment of APOL1 on renal disease
-
Friedman DJ, Kozlitina J, Genovese G et al. Population-based risk assessment of APOL1 on renal disease. J Am Soc Nephrol 2011; 22: 2098-2105
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 2098-2105
-
-
Friedman, D.J.1
Kozlitina, J.2
Genovese, G.3
-
10
-
-
80555148890
-
Genetic variation in APOL1 associates with younger age at hemodialysis initiation
-
Kanji Z, Powe CE, Wenger JB et al. Genetic variation in APOL1 associates with younger age at hemodialysis initiation. J Am Soc Nephrol 2011; 22: 2091-2097
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 2091-2097
-
-
Kanji, Z.1
Powe, C.E.2
Wenger, J.B.3
-
11
-
-
79955529193
-
The APOL1 gene and allograft survival after kidney transplantation
-
Reeves-Daniel AM, DePalma JA, Bleyer AJ et al. The APOL1 gene and allograft survival after kidney transplantation. Am J Transplant 2011; 11: 1025-1030
-
(2011)
Am J Transplant
, vol.11
, pp. 1025-1030
-
-
Reeves-Daniel, A.M.1
Depalma, J.A.2
Bleyer, A.J.3
-
12
-
-
79957491313
-
The MYH9/APOL1 region and chronic kidney disease in European-Americans
-
O'Seaghdha CM, Parekh RS, Hwang SJ et al. The MYH9/APOL1 region and chronic kidney disease in European-Americans. Hum Mol Genet 2011; 20: 2450-2456
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2450-2456
-
-
O'seaghdha, C.M.1
Parekh, R.S.2
Hwang, S.J.3
-
13
-
-
84859314693
-
Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans
-
Cooke JN, Bostrom MA, Hicks PJ et al. Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans. Nephrol Dial Transplant 2012; 27: 1505-1511
-
(2012)
Nephrol Dial Transplant
, vol.27
, pp. 1505-1511
-
-
Cooke, J.N.1
Bostrom, M.A.2
Hicks, P.J.3
-
14
-
-
0034755959
-
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes
-
Heath KE, Campos-Barros A, Toren A et al. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am J Hum Genet 2001; 69: 1033-1045
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1033-1045
-
-
Heath, K.E.1
Campos-Barros, A.2
Toren, A.3
-
15
-
-
0037910378
-
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
-
SeriM, Pecci A, Di Bari F et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 2003; 82: 203-215
-
(2003)
Medicine (Baltimore)
, vol.82
, pp. 203-215
-
-
Seri, M.1
Pecci, A.2
Di Bari, F.3
-
16
-
-
18244406592
-
Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions
-
Kunishima S, Matsushita T, Kojima T et al. Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions. J Hum Genet 2001; 46: 722-729
-
(2001)
J Hum Genet
, vol.46
, pp. 722-729
-
-
Kunishima, S.1
Matsushita, T.2
Kojima, T.3
-
17
-
-
77954224966
-
Glomerular pathology in autosomal dominant MYH9 spectrum disorders: What are the clues telling us about disease mechanism?
-
Kopp JB. Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism? Kidney Int 2010; 78: 130-133
-
(2010)
Kidney Int
, vol.78
, pp. 130-133
-
-
Kopp, J.B.1
-
18
-
-
9844267961
-
Normal distribution of collagen IV in renal basement membranes in Epstein's syndrome
-
Naito I, Nomura S, Inoue S et al. Normal distribution of collagen IV in renal basement membranes in Epstein's syndrome. J Clin Pathol 1997; 50: 919-922
-
(1997)
J Clin Pathol
, vol.50
, pp. 919-922
-
-
Naito, I.1
Nomura, S.2
Inoue, S.3
-
19
-
-
77954242769
-
Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease
-
Sekine T, Konno M, Sasaki S et al. Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease. Kidney Int 2010; 78: 207-214
-
(2010)
Kidney Int
, vol.78
, pp. 207-214
-
-
Sekine, T.1
Konno, M.2
Sasaki, S.3
-
20
-
-
84862908887
-
Mouse models of MYH9-related disease: Mutations in nonmuscle myosin II-A
-
Zhang Y, Conti MA, Malide D et al. Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A. Blood 2012; 119: 238-250
-
(2012)
Blood
, vol.119
, pp. 238-250
-
-
Zhang, Y.1
Conti, M.A.2
Malide, D.3
-
21
-
-
79956071512
-
Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy
-
Johnstone DB, Zhang J, George B et al. Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy. Mol Cell Biol 2011; 31: 2162-2170
-
(2011)
Mol Cell Biol
, vol.31
, pp. 2162-2170
-
-
Johnstone, D.B.1
Zhang, J.2
George, B.3
-
22
-
-
0026557199
-
Myosin II distribution in neurons is consistent with a role in growth cone motility but not synaptic vesicle mobilization
-
Miller M, Bower E, Levitt P et al. Myosin II distribution in neurons is consistent with a role in growth cone motility but not synaptic vesicle mobilization. Neuron 1992; 8: 25-44
-
(1992)
Neuron
, vol.8
, pp. 25-44
-
-
Miller, M.1
Bower, E.2
Levitt, P.3
-
23
-
-
0035865524
-
Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
-
Kunishima S, Kojima T, Matsushita T et al. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). Blood 2001; 97: 1147-1149
-
(2001)
Blood
, vol.97
, pp. 1147-1149
-
-
Kunishima, S.1
Kojima, T.2
Matsushita, T.3
-
24
-
-
8844261172
-
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: Hematological, nephrological, and otological studies of heterozygous KO mice
-
Matsushita T, Hayashi H, Kunishima S et al. Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice. Biochem Biophys Res Com 2004; 325: 1163-1171
-
(2004)
Biochem Biophys Res Com
, vol.325
, pp. 1163-1171
-
-
Matsushita, T.1
Hayashi, H.2
Kunishima, S.3
-
25
-
-
0033983608
-
Non-muscle myosin IIB-like immunoreactivity is present at the drebrin-binding cytoskeleton in neurons
-
Cheng XT, Hayashi K, Shirao T. Non-muscle myosin IIB-like immunoreactivity is present at the drebrin-binding cytoskeleton in neurons. Neurosci Res 2000; 36: 167-173
-
(2000)
Neurosci Res
, vol.36
, pp. 167-173
-
-
Cheng, X.T.1
Hayashi, K.2
Shirao, T.3
-
26
-
-
67649778673
-
Phosphorylation of nephrin triggers Ca2+ signaling by recruitment and activation of phospholipase C-gamma
-
Harita Y, Kurihara H, Kosako H et al. Phosphorylation of nephrin triggers Ca2+ signaling by recruitment and activation of phospholipase C-gamma. J Biol Chem 2009; 284: 8951-8962
-
(2009)
J Biol Chem
, vol.284
, pp. 8951-8962
-
-
Harita, Y.1
Kurihara, H.2
Kosako, H.3
-
27
-
-
44049087922
-
Neph1, a component of the kidney slit diaphragm, is tyrosine- phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2
-
Harita Y, Kurihara H, Kosako H et al. Neph1, a component of the kidney slit diaphragm, is tyrosine-phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2. J Biol Chem 2008; 283: 9177-9186
-
(2008)
J Biol Chem
, vol.283
, pp. 9177-9186
-
-
Harita, Y.1
Kurihara, H.2
Kosako, H.3
-
28
-
-
84865216663
-
SIRPα interacts with nephrin at the podocyte slit diaphragm
-
Kajiho Y, Harita Y, Kurihara H et al. SIRPα interacts with nephrin at the podocyte slit diaphragm. FEBS J 2012; 279: 3010-3021
-
(2012)
FEBS J
, vol.279
, pp. 3010-3021
-
-
Kajiho, Y.1
Harita, Y.2
Kurihara, H.3
-
29
-
-
0031830798
-
Monoclonal antibody P-31 recognizes a novel intermediate filament-associated protein (p250) in rat podocytes
-
Kurihara H, Sunagawa N, Kobayashi T et al. Monoclonal antibody P-31 recognizes a novel intermediate filament-associated protein (p250) in rat podocytes. Am J Physiol 1998; 274: F986-F997
-
(1998)
Am J Physiol
, vol.274
-
-
Kurihara, H.1
Sunagawa, N.2
Kobayashi, T.3
-
30
-
-
0037377624
-
Intussusceptive capillary growth is required for glomerular repair in rat Thy-1. 1 nephritis
-
Notoya M, Shinosaki T, Kobayashi T et al. Intussusceptive capillary growth is required for glomerular repair in rat Thy-1.1 nephritis. Kidney Int 2003; 63: 1365-1373
-
(2003)
Kidney Int
, vol.63
, pp. 1365-1373
-
-
Notoya, M.1
Shinosaki, T.2
Kobayashi, T.3
-
31
-
-
0024318954
-
Use of poly(vinylpyrrolidone) and poly(vinyl alcohol) for cryoultramicrotomy
-
Tokuyasu KT. Use of poly(vinylpyrrolidone) and poly(vinyl alcohol) for cryoultramicrotomy. Histochem J 1989; 21: 163-171
-
(1989)
Histochem J
, vol.21
, pp. 163-171
-
-
Tokuyasu, K.T.1
-
32
-
-
33645577952
-
Upregulation of nestin, vimentin, and desmin in rat podocytes in response to injury
-
Zou J, Yaoita E,Watanabe Y et al. Upregulation of nestin, vimentin, and desmin in rat podocytes in response to injury. Virchows Arch 2006; 448: 485-492
-
(2006)
Virchows Arch
, vol.448
, pp. 485-492
-
-
Zou, J.1
Yaoita, E.2
Watanabe, Y.3
-
33
-
-
33745039299
-
Immunoexpression of podocyte-associated preteins in acquired human glomerulopathies with nephrotic syndrome
-
Wagrowska-Danilewicz M, Stasikowska O, Danilewicz M. Immunoexpression of podocyte-associated preteins in acquired human glomerulopathies with nephrotic syndrome. Pol J Pathol 2006; 57: 17-21
-
(2006)
Pol J Pathol
, vol.57
, pp. 17-21
-
-
Wagrowska-Danilewicz, M.1
Stasikowska, O.2
Danilewicz, M.3
-
35
-
-
1542359928
-
Expression of nephrin in acquired forms of nephrotic syndrome in childhood
-
Hingorani SR, Finn LS, Kowalewska J et al. Expression of nephrin in acquired forms of nephrotic syndrome in childhood. Pediatr Nephrol 2004; 19: 300-305
-
(2004)
Pediatr Nephrol
, vol.19
, pp. 300-305
-
-
Hingorani, S.R.1
Finn, L.S.2
Kowalewska, J.3
-
36
-
-
12244254488
-
Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome
-
Wernerson A, Duner F, Pettersson E et al. Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome. Nephrol Dial Transplant 2003; 18: 70-76
-
(2003)
Nephrol Dial Transplant
, vol.18
, pp. 70-76
-
-
Wernerson, A.1
Duner, F.2
Pettersson, E.3
-
37
-
-
0242441925
-
Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome
-
Guan N, Ding J, Zhang J et al. Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome. Pediatr Nephrol. 2003; 18: 1122-1127
-
(2003)
Pediatr Nephrol.
, vol.18
, pp. 1122-1127
-
-
Guan, N.1
Ding, J.2
Zhang, J.3
-
38
-
-
0041842626
-
Expression of podocyteassociated molecules in acquired human kidney diseases
-
Koop K, Eikmans M, Baelde HJ et al. Expression of podocyteassociated molecules in acquired human kidney diseases. J Am Soc Nephrol 2003; 14: 2063-2071
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 2063-2071
-
-
Koop, K.1
Eikmans, M.2
Baelde, H.J.3
-
40
-
-
0036138503
-
Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes
-
Arrondel C, Vodovar N, Knebelmann B et al. Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes. J Am Soc Nephrol 2002; 13: 65-74
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 65-74
-
-
Arrondel, C.1
Vodovar, N.2
Knebelmann, B.3
-
41
-
-
0037225967
-
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
-
Ghiggeri GM, Caridi G, Magrini U et al. Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome). Am J Kidney Dis 2003; 41: 95-104
-
(2003)
Am J Kidney Dis
, vol.41
, pp. 95-104
-
-
Ghiggeri, G.M.1
Caridi, G.2
Magrini, U.3
-
42
-
-
66549123467
-
Of mice and men: Relevance of cellular and molecular characterizations of myosin IIA to MYH9-related human disease
-
Even-Ram S, Yamada KM.: Of mice and men: relevance of cellular and molecular characterizations of myosin IIA to MYH9-related human disease. Cell Adh Migr 2007; 1: 152-155
-
(2007)
Cell Adh Migr
, vol.1
, pp. 152-155
-
-
Even-Ram, S.1
Yamada, K.M.2
-
43
-
-
80052435507
-
Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes
-
Babayeva S, Miller M, Zilber Y et al. Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes. Pediatr Nephrol 2011; 26: 1071-1081
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 1071-1081
-
-
Babayeva, S.1
Miller, M.2
Zilber, Y.3
|