-
1
-
-
68449084423
-
T regulatory cell function in idiopathic minimal lesion nephrotic syndrome
-
19495805 10.1007/s00467-009-1214-x
-
C Araya L Diaz C Wasserfall, et al. 2009 T regulatory cell function in idiopathic minimal lesion nephrotic syndrome Pediatr Nephrol 24 9 1691 1698 19495805 10.1007/s00467-009-1214-x
-
(2009)
Pediatr Nephrol
, vol.24
, Issue.9
, pp. 1691-1698
-
-
Araya, C.1
Diaz, L.2
Wasserfall, C.3
-
2
-
-
34250784012
-
The role of the Wilms tumour gene (WT1) in normal and malignant haematopoiesis
-
DOI 10.1017/S1462399407000336, PII S1462399407000336
-
S Ariyaratana DM Loeb 2007 The role of the Wilms tumour gene (WT1) in normal and malignant haematopoiesis Expert Rev Mol Med 9 1 17 17524167 10.1017/S1462399407000336 (Pubitemid 46965072)
-
(2007)
Expert Reviews in Molecular Medicine
, vol.9
, Issue.14
, pp. 1-17
-
-
Ariyaratana, S.1
Loeb, D.M.2
-
3
-
-
33747822319
-
WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes
-
DOI 10.1007/s00467-006-0225-0
-
F Aucella L Bisceglia P De Bonis, et al. 2006 WT1 mutations in nephrotic syndrome revisited. high prevalence in young girls, associations and renal phenotypes Pediatr Nephrol 21 1393 1398 16909243 10.1007/s00467-006-0225-0 (Pubitemid 44283470)
-
(2006)
Pediatric Nephrology
, vol.21
, Issue.10
, pp. 1393-1398
-
-
Aucella, F.1
Bisceglia, L.2
Bonis, P.3
Gigante, M.4
Caridi, G.5
Barbano, G.6
Mattioli, G.7
Perfumo, F.8
Gesualdo, L.9
Ghiggeri, G.M.10
-
4
-
-
0028116649
-
Mesangial cell apoptosis: The major mechanism for resolution of glomerular hypercellularity in experimental mesangial proliferative nephritis
-
AJ Baker A Mooney J Hughes, et al. 1994 Mesangial cell apoptosis: the major mechanism for resolution of glomerular hypercellularity in experimental mesangial proliferative nephritis J Clin Invest 94 2105 2116 7962557 10.1172/JCI117565 1:CAS:528:DyaK2MXhvFKgs7o%3D (Pubitemid 24348252)
-
(1994)
Journal of Clinical Investigation
, vol.94
, Issue.5
, pp. 2105-2116
-
-
Baker, A.J.1
Mooney, A.2
Hughes, J.3
Lombardi, D.4
Johnson, R.J.5
Savill, J.6
-
5
-
-
16944365351
-
Donor splice-site mutations in WT1 are responsible for Frasier syndrome
-
S Barbaux P Niaudet MC Gubler, et al. 1997 Donor splice-site mutations in WT1 are responsible for Frasier syndrome Nat Genet 17 467 470 9398852 10.1038/ng1297-467 1:CAS:528:DyaK2sXnvFWrsrY%3D (Pubitemid 27518399)
-
(1997)
Nature Genetics
, vol.17
, Issue.4
, pp. 467-470
-
-
Barbaux, S.1
Niaudet, P.2
Gubler, M.-C.3
Grunfeld, J.-P.4
Jaubert, F.5
Kuttenn, F.6
Fekete, C.N.7
Souleyreau-Therville, N.8
Thibaud, E.9
Fellous, M.10
McElreavey, K.11
-
6
-
-
67349134171
-
Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1
-
19205749 10.1007/s00467-009-1135-8
-
D Bockenhauer W van't Hoff G Chernin, et al. 2009 Membranoproliferative glomerulonephritis associated with a mutation in Wilms' tumour suppressor gene 1 Pediatr Nephrol 24 1399 1401 19205749 10.1007/s00467-009-1135-8
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 1399-1401
-
-
Bockenhauer, D.1
Van'T Hoff, W.2
Chernin, G.3
-
7
-
-
78149355246
-
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome
-
20798252 10.2215/CJN.01190210
-
AK Büscher B Kranz R Büscher, et al. 2010 Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome Clin J Am Soc Nephrol 5 2075 2084 20798252 10.2215/CJN.01190210
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, pp. 2075-2084
-
-
Büscher, A.K.1
Kranz, B.2
Büscher, R.3
-
8
-
-
1642514813
-
Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation
-
DOI 10.1093/hmg/ddh015
-
JA Davies M Ladomery P Hohenstein, et al. 2004 Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation Hum Mol Genet 13 235 246 14645201 10.1093/hmg/ddh015 1:CAS:528:DC%2BD2cXmsVGl (Pubitemid 38111361)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.2
, pp. 235-246
-
-
Davies, J.A.1
Ladomery, M.2
Hohenstein, P.3
Michael, L.4
Shafe, A.5
Spraggon, L.6
Hestie, N.7
-
9
-
-
0014119131
-
Association d'un syndrome anatomo-pathologique de pseudohermaphroditismue masculinum, d'une tumeur de Wilms, d'une nephropathie parenchymateuse et d'un mosaicisme XX/XY
-
4292870 1:STN:280:DyaF1c%2FgtlKrtA%3D%3D
-
P Denys P Malvaux H Van den Berghe, et al. 1967 Association d'un syndrome anatomo-pathologique de pseudohermaphroditismue masculinum, d'une tumeur de Wilms, d'une nephropathie parenchymateuse et d'un mosaicisme XX/XY Arch Fr Pediatr 24 729 739 4292870 1:STN:280:DyaF1c%2FgtlKrtA%3D%3D
-
(1967)
Arch Fr Pediatr
, vol.24
, pp. 729-739
-
-
Denys, P.1
Malvaux, P.2
Van Den Berghe, H.3
-
10
-
-
0014775569
-
Syndrome of pseudohermaphroditism, Wilms' tumor, hypertension and degenerative renal disease
-
4316066 10.1016/S0022-3476(70)80409-7 1:STN:280:DyaE3c3gs12ktA%3D%3D
-
A Drash F Sherman WH Hartman RM Blizzard, et al. 1970 Syndrome of pseudohermaphroditism, Wilms' tumor, hypertension and degenerative renal disease J Pediatr 76 585 593 4316066 10.1016/S0022-3476(70)80409-7 1:STN:280: DyaE3c3gs12ktA%3D%3D
-
(1970)
J Pediatr
, vol.76
, pp. 585-593
-
-
Drash, A.1
Sherman, F.2
Hartman, W.H.3
Blizzard, R.M.4
-
11
-
-
0027405362
-
In vivo induction of interleukin 10 by anti-CD3 monoclonal antibody or bacterial lipopolysaccharide: Differential modulation by cyclosporin A
-
P Durez D Abramowicz C Gérard, et al. 1993 In vivo induction of interleukin 10 by anti-CD3 monoclonal antibody or bacterial lipopolysaccharide: differential modulation by cyclosporin A J Exp Med 177 551 555 8426125 10.1084/jem.177.2.551 1:CAS:528:DyaK3sXnvFWhsg%3D%3D (Pubitemid 23117108)
-
(1993)
Journal of Experimental Medicine
, vol.177
, Issue.2
, pp. 551-555
-
-
Durez, P.1
Abramowicz, D.2
Gerard, C.3
Van Mechelen, M.4
Amraoui, Z.5
Dubois, C.6
Leo, O.7
Velu, T.8
Goldman, M.9
-
12
-
-
34547851718
-
Steroid-resistant idiopathic childhood nephrosis: Overdiagnosed and undertreated
-
DOI 10.1093/ndt/gfm092
-
JH Ehrich C Geerlings M Zivicnjak, et al. 2007 Steroid-resistant idiopathic childhood nephrosis: overdiagnosed and undertreated Nephrol Dial Transplant 22 2183 2193 17504846 10.1093/ndt/gfm092 (Pubitemid 47244695)
-
(2007)
Nephrology Dialysis Transplantation
, vol.22
, Issue.8
, pp. 2183-2193
-
-
Ehrich, J.H.H.1
Geerlings, C.2
Zivicnjak, M.3
Franke, D.4
Geerlings, H.5
Gellermann, J.6
-
13
-
-
51349162919
-
The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A
-
18724379 10.1038/nm.1857 1:CAS:528:DC%2BD1cXhtVyms7%2FJ
-
C Faul M Donnelly S Merscher-Gomez, et al. 2008 The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A Nat Med 14 931 938 18724379 10.1038/nm.1857 1:CAS:528: DC%2BD1cXhtVyms7%2FJ
-
(2008)
Nat Med
, vol.14
, pp. 931-938
-
-
Faul, C.1
Donnelly, M.2
Merscher-Gomez, S.3
-
14
-
-
0000786264
-
Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins
-
14149008 10.1016/S0022-3476(64)80622-3 1:STN:280:DyaF2c7gs12guw%3D%3D
-
S Frasier R Bashore H Mosllur 1964 Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins J Pediatr 64 740 745 14149008 10.1016/S0022-3476(64)80622-3 1:STN:280:DyaF2c7gs12guw%3D%3D
-
(1964)
J Pediatr
, vol.64
, pp. 740-745
-
-
Frasier, S.1
Bashore, R.2
Mosllur, H.3
-
15
-
-
42949101458
-
Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)
-
DOI 10.1093/ndt/gfm759
-
R Gbadegesin BG Hinkes BE Hoskins, et al. 2008 Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) Nephrol Dial Transplant 23 1291 1297 18065803 10.1093/ndt/gfm759 1:CAS:528: DC%2BD1cXjs12lt7w%3D (Pubitemid 351767487)
-
(2008)
Nephrology Dialysis Transplantation
, vol.23
, Issue.4
, pp. 1291-1297
-
-
Gbadegesin, R.1
Hinkes, B.G.2
Hoskins, B.E.3
Vlangos, C.N.4
Heeringa, S.F.5
Liu, J.6
Loirat, C.7
Ozaltin, F.8
Hashmi, S.9
Ulmer, F.10
Cleper, R.11
Ettenger, R.12
Antignac, C.13
Wiggins, R.C.14
Zenker, M.15
Hildebrandt, F.16
-
16
-
-
77954534482
-
Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations
-
20191369 10.1007/s00467-010-1468-3
-
J Gellermann CJ Stefanidis A Mitsioni U Querfeld 2010 Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations Pediatr Nephrol 25 1285 1289 20191369 10.1007/s00467-010-1468-3
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 1285-1289
-
-
Gellermann, J.1
Stefanidis, C.J.2
Mitsioni, A.3
Querfeld, U.4
-
17
-
-
0034653547
-
Mechanisms of cyclosporine A-induced apoptosis in rat hepatocyte primary cultures
-
DOI 10.1006/taap.1999.8887
-
S Grub E Persohn WE Trommer, et al. 2000 Mechanisms of cyclosporine A-induced apoptosis in rat hepatocyte primary cultures Toxicol Appl Pharmacol 163 209 220 10702360 10.1006/taap.1999.8887 1:CAS:528:DC%2BD3cXhsV2js7o%3D (Pubitemid 30158550)
-
(2000)
Toxicology and Applied Pharmacology
, vol.163
, Issue.3
, pp. 209-220
-
-
Grub, S.1
Persohn, E.2
Trommer, W.E.3
Wolf, A.4
-
18
-
-
0038512591
-
Podocyte differentiation and hereditary proteinuria/nephrotic syndromes
-
12761234 10.1097/01.ASN.0000067648.75923.68
-
MC Gubler 2003 Podocyte differentiation and hereditary proteinuria/nephrotic syndromes J Am Soc Nephrol 14 S22 26 12761234 10.1097/01.ASN.0000067648.75923.68
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 22-26
-
-
Gubler, M.C.1
-
19
-
-
0037087593
-
WT1 is a key regulator of podocyte function: Reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis
-
JK Guo AL Menke MC Gubler, et al. 2002 WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis Hum Mol Genet 11 651 659 11912180 10.1093/hmg/11.6.651 1:CAS:528:DC%2BD38XivV2ntL4%3D (Pubitemid 34285136)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.6
, pp. 651-659
-
-
Guo, J.-K.1
Menke, A.L.2
Gubler, M.-C.3
Clarke, A.R.4
Harrison, D.5
Hammes, A.6
Hastie, N.D.7
Schedl, A.8
-
20
-
-
0025288793
-
An internal deletion within a 11p13 zinc finger gene contributes to the development of Wilms' tumor
-
DOI 10.1016/0092-8674(90)90690-G
-
DA Haber AJ Buckler T Glaser, et al. 1990 An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor Cell 61 1257 1269 2163761 10.1016/0092-8674(90)90690-G 1:CAS:528:DyaK3cXltFSgsLo%3D (Pubitemid 20208830)
-
(1990)
Cell
, vol.61
, Issue.7
, pp. 1257-1269
-
-
Haber, D.A.1
Buckler, A.J.2
Glaser, T.3
Call, K.M.4
Pelletier, J.5
Sohn, R.L.6
Douglass, E.C.7
Housman, D.E.8
-
21
-
-
0027342443
-
Diffuse mesangial sclerosis: A congenital glomerulopathy with nephrotic syndrome
-
8381254 1:STN:280:DyaK3s7ltFShtA%3D%3D
-
R Habib MC Gubler C Antignac, et al. 1993 Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome Adv Nephrol Necker Hosp 22 43 57 8381254 1:STN:280:DyaK3s7ltFShtA%3D%3D
-
(1993)
Adv Nephrol Necker Hosp
, vol.22
, pp. 43-57
-
-
Habib, R.1
Gubler, M.C.2
Antignac, C.3
-
22
-
-
0023897646
-
Cell death in the diseased glomerulus
-
3417249 10.1111/j.1365-2559.1988.tb01995.x 1:STN:280:DyaL1czivF2rtw%3D%3D
-
DJ Harrison 1988 Cell death in the diseased glomerulus Histopathology 12 679 683 3417249 10.1111/j.1365-2559.1988.tb01995.x 1:STN:280: DyaL1czivF2rtw%3D%3D
-
(1988)
Histopathology
, vol.12
, pp. 679-683
-
-
Harrison, D.J.1
-
23
-
-
49349092291
-
The role of the Wilms' tumour-suppressor protein WT1 in apoptosis
-
18631130 10.1042/BST0360629 1:CAS:528:DC%2BD1cXoslClt7Y%3D
-
J Hartkamp SG Roberts 2008 The role of the Wilms' tumour-suppressor protein WT1 in apoptosis Biochem Soc Trans 36 629 631 18631130 10.1042/BST0360629 1:CAS:528:DC%2BD1cXoslClt7Y%3D
-
(2008)
Biochem Soc Trans
, vol.36
, pp. 629-631
-
-
Hartkamp, J.1
Roberts, S.G.2
-
24
-
-
33751531864
-
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
-
DOI 10.1038/ng1918, PII NG1918
-
B Hinkes RC Wiggins R Gbadegesin, et al. 2006 Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible Nat Genet Dec 38 12 1397 1405 10.1038/ng1918 1:CAS:528: DC%2BD28Xht1CntrfO (Pubitemid 44837561)
-
(2006)
Nature Genetics
, vol.38
, Issue.12
, pp. 1397-1405
-
-
Hinkes, B.1
Wiggins, R.C.2
Gbadegesin, R.3
Vlangos, C.N.4
Seelow, D.5
Nurnberg, G.6
Garg, P.7
Verma, R.8
Chaib, H.9
Hoskins, B.E.10
Ashraf, S.11
Becker, C.12
Hennies, H.C.13
Goyal, M.14
Wharram, B.L.15
Schachter, A.D.16
Mudumana, S.17
Drummond, I.18
Kerjaschki, D.19
Waldherr, R.20
Dietrich, A.21
Ozaltin, F.22
Bakkaloglu, A.23
Cleper, R.24
Basel-Vanagaite, L.25
Pohl, M.26
Griebel, M.27
Tsygin, A.N.28
Soylu, A.29
Muller, D.30
Sorli, C.S.31
Bunney, T.D.32
Katan, M.33
Liu, J.34
Attanasio, M.35
O'Toole, J.F.36
Hasselbacher, K.37
Mucha, B.38
Otto, E.A.39
Airik, R.40
Kispert, A.41
Kelley, G.G.42
Smrcka, A.V.43
Gudermann, T.44
Holzman, L.B.45
Nurnberg, P.46
Hildebrandt, F.47
more..
-
25
-
-
34147096001
-
Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)
-
DOI 10.1542/peds.2006-2164
-
BG Hinkes B Mucha CN Vlangos, et al. 2007 Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2) Pediatrics 119 e907 919 17371932 10.1542/peds.2006-2164 (Pubitemid 46556655)
-
(2007)
Pediatrics
, vol.119
, Issue.4
-
-
Hinkes, B.G.1
Mucha, B.2
Vlangos, C.N.3
Gbadegesin, R.4
Liu, J.5
Hasselbacher, K.6
Hangan, D.7
Ozaltin, F.8
Zenker, M.9
Hildebrandt, F.10
-
26
-
-
33749031535
-
The many facets of the Wilms' tumour gene, WT1
-
DOI 10.1093/hmg/ddl196
-
P Hohenstein ND Hastie 2006 The many facets of the Wilms' tumour gene, WT1 Hum Mol Genet 15 196 201 10.1093/hmg/ddl196 (Pubitemid 44446794)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.SUPPL. 2
-
-
Hohenstein, P.1
Hastie, N.D.2
-
27
-
-
34547851696
-
Familial nephrotic syndrome: PLCE1 enters the fray
-
DOI 10.1093/ndt/gfm098
-
JA Jefferson SJ Shankland 2007 Familial nephrotic syndrome: PLCE1 enters the fray Nephrol Dial Transplant 22 1849 1852 17449496 10.1093/ndt/gfm098 (Pubitemid 47244751)
-
(2007)
Nephrology Dialysis Transplantation
, vol.22
, Issue.7
, pp. 1849-1852
-
-
Jefferson, J.A.1
Shankland, S.J.2
-
28
-
-
0036248087
-
Interleukin-10 inhibits experimental mesangial proliferative glomerulonephritis
-
DOI 10.1046/j.1365-2249.2002.01793.x
-
AR Kitching M Katerelos SJ Mudge, et al. 2002 Interleukin-10 inhibits experimental mesangial proliferative glomerulonephritis Clin Exp Immunol 128 36 43 11982588 10.1046/j.1365-2249.2002.01793.x 1:CAS:528:DC%2BD38XksFSmtL4%3D (Pubitemid 34451177)
-
(2002)
Clinical and Experimental Immunology
, vol.128
, Issue.1
, pp. 36-43
-
-
Kitching, A.R.1
Katerelos, M.2
Mudge, S.J.3
Tipping, P.G.4
Power, D.A.5
Holdsworth, S.R.6
-
29
-
-
0031922880
-
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms
-
DOI 10.1093/hmg/7.4.709
-
B Klamt A Koziell F Poulat, et al. 1998 Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 KTS splice isoforms Hum Mol Genet 7 709 14 9499425 10.1093/hmg/7.4.709 1:CAS:528:DyaK1cXisVCjur0%3D (Pubitemid 28152270)
-
(1998)
Human Molecular Genetics
, vol.7
, Issue.4
, pp. 709-714
-
-
Klamt, B.1
Koziell, A.2
Poulat, F.3
Wieacker, P.4
Scambler, P.5
Berta, P.6
Gessler, M.7
-
30
-
-
0027182741
-
WT-1 is required for early kidney development
-
DOI 10.1016/0092-8674(93)90515-R
-
JA Kreidberg H Sariola JM Loring M Maeda J Pelletier D Housman R Jaenisch 1993 WT-1 is required for early kidney development Cell 74 679 691 8395349 10.1016/0092-8674(93)90515-R 1:CAS:528:DyaK3sXlsFKrurg%3D (Pubitemid 23259748)
-
(1993)
Cell
, vol.74
, Issue.4
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
Loring, J.M.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jaenisch, R.7
-
31
-
-
33745143994
-
WT1 influences apoptosis through transcriptional regulation of Bcl-2 family members
-
DM Loeb 2006 WT1 influences apoptosis through transcriptional regulation of Bcl-2 family members Cell Cycle 12 1249 1253 10.4161/cc.5.12.2807 (Pubitemid 43894273)
-
(2006)
Cell Cycle
, vol.5
, Issue.12
, pp. 1249-1253
-
-
Loeb, D.M.1
-
32
-
-
70349621624
-
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis-a review
-
19562370 10.1007/s00431-009-1017-x
-
MM Löwik PJ Groenen EN Levtchenko, et al. 2009 Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis-a review Eur J Pediatr 168 1291 1304 19562370 10.1007/s00431-009-1017-x
-
(2009)
Eur J Pediatr
, vol.168
, pp. 1291-1304
-
-
Löwik, M.M.1
Groenen, P.J.2
Levtchenko, E.N.3
-
33
-
-
70149084338
-
Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation
-
19495806 10.1007/s00467-009-1211-0
-
M Malina O Cinek J Janda T Seeman 2009 Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation Pediatr Nephrol 24 2051 2053 19495806 10.1007/s00467-009-1211-0
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 2051-2053
-
-
Malina, M.1
Cinek, O.2
Janda, J.3
Seeman, T.4
-
34
-
-
67650077702
-
Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome
-
10.1089/gtmb.2008.0083
-
S Megremis A Mitsioni AG Mitsioni, et al. 2009 Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome Genet Test Mol Biomarkers 2 249 256 10.1089/gtmb.2008.0083
-
(2009)
Genet Test Mol Biomarkers
, vol.2
, pp. 249-256
-
-
Megremis, S.1
Mitsioni, A.2
Mitsioni, A.G.3
-
35
-
-
0642282020
-
WT1 and glomerular function
-
DOI 10.1016/S1084-9521(03)00026-0
-
AL Menke A Schedl 2003 WT1 and glomerular function Semin Cell Dev Biol 14 233 240 14627122 10.1016/S1084-9521(03)00026-0 1:CAS:528:DC%2BD3sXosFyltrw%3D (Pubitemid 38160960)
-
(2003)
Seminars in Cell and Developmental Biology
, vol.14
, Issue.4
, pp. 233-240
-
-
Menke, A.L.1
Schedl, A.2
-
36
-
-
69449101369
-
Increased interleukin-10 production without expansion of CD4? T-regulatory cells in early stable renal transplant patients on calcineurin inhibitors
-
19667950 10.1097/TP.0b013e3181af20fd 1:CAS:528:DC%2BD1MXpsFyhtbc%3D
-
SK Mittal RK Sharma A Gupta S Naik 2009 Increased interleukin-10 production without expansion of CD4? T-regulatory cells in early stable renal transplant patients on calcineurin inhibitors Transplantation 88 435 441 19667950 10.1097/TP.0b013e3181af20fd 1:CAS:528:DC%2BD1MXpsFyhtbc%3D
-
(2009)
Transplantation
, vol.88
, pp. 435-441
-
-
Mittal, S.K.1
Sharma, R.K.2
Gupta, A.3
Naik, S.4
-
37
-
-
33745143094
-
The Wilms tumour suppressor protein WT1 (+KTS isoform) binds alpha-actinin 1 mRNA via its zinc-finger domain
-
DOI 10.1139/O06-065
-
AA Morrison JP Venables G Dellaire, et al. 2006 The Wilms tumour suppressor protein WT1 (? isoform) binds alpha-actinin 1 mRNA via its zinc-finger domain Biochem Cell Biol 84 789 798 17167543 10.1139/o06-065 1:CAS:528:DC%2BD2sXosVc%3D (Pubitemid 46121604)
-
(2006)
Biochemistry and Cell Biology
, vol.84
, Issue.5
, pp. 789-798
-
-
Morrison, A.A.1
Venables, J.P.2
Dellaire, G.3
Ladomery, M.R.4
-
38
-
-
24944496261
-
WT1 induces apoptosis through transcriptional regulation of the proapoptotic Bcl-2 family member Bak
-
DOI 10.1158/0008-5472.CAN-04-3657
-
DJ Morrison MA English JD Licht 2005 WT1 induces apoptosis through transcriptional regulation of the proapoptotic Bcl-2 family member Bak Cancer Res 65 8174 8182 16166292 10.1158/0008-5472.CAN-04-3657 1:CAS:528: DC%2BD2MXhtVShsbvI (Pubitemid 41330581)
-
(2005)
Cancer Research
, vol.65
, Issue.18
, pp. 8174-8182
-
-
Morrison, D.J.1
English, M.A.2
Licht, J.D.3
-
39
-
-
36549081348
-
CD4 regulatory T cells: From basic research to potential therapeutic use
-
18027108 1:CAS:528:DC%2BD2sXhsVGitbrP
-
C Mottet D Golshayan 2007 CD4 regulatory T cells: from basic research to potential therapeutic use Swiss Med Wkly 137 625 634 18027108 1:CAS:528:DC%2BD2sXhsVGitbrP
-
(2007)
Swiss Med Wkly
, vol.137
, pp. 625-634
-
-
Mottet, C.1
Golshayan, D.2
-
40
-
-
33748702059
-
WT1 and glomerular diseases
-
DOI 10.1007/s00467-006-0208-1
-
P Niaudet MC Gubler 2006 WT1 and glomerular diseases Pediatr Nephrol 21 1653 1660 16927106 10.1007/s00467-006-0208-1 (Pubitemid 44390829)
-
(2006)
Pediatric Nephrology
, vol.21
, Issue.11
, pp. 1653-1660
-
-
Niaudet, P.1
Gubler, M.-C.2
-
41
-
-
0035856480
-
WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin
-
DOI 10.1016/S0960-9822(01)00560-7
-
RE Palmer A Kotsianti B Cadman, et al. 2001 WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin Curr Biol 11 22 1805 1809 11719225 10.1016/S0960-9822(01)00560-7 1:CAS:528:DC%2BD3MXos1KlsLo%3D (Pubitemid 33092171)
-
(2001)
Current Biology
, vol.11
, Issue.22
, pp. 1805-1809
-
-
Palmer, R.E.1
Kotsianti, A.2
Cadman, B.3
Boyd, T.4
Gerald, W.5
Haber, D.A.6
-
42
-
-
77649321533
-
A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes
-
19797313 10.1093/hmg/ddp462 1:CAS:528:DC%2BD1MXhsFGhu7jI
-
J Ratelade C Arrondel G Hamard, et al. 2010 A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes Hum Mol Genet 19 1 1 15 19797313 10.1093/hmg/ddp462 1:CAS:528:DC%2BD1MXhsFGhu7jI
-
(2010)
Hum Mol Genet
, vol.19
, Issue.1
, pp. 1-15
-
-
Ratelade, J.1
Arrondel, C.2
Hamard, G.3
-
43
-
-
0017883401
-
Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p Interstitial deletion
-
208044 1:STN:280:DyaE1c3gtFWrtw%3D%3D
-
VM Riccardi E Sujansky AC Smith, et al. 1978 Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p Interstitial deletion Pediatrics 61 604 610 208044 1:STN:280:DyaE1c3gtFWrtw%3D%3D
-
(1978)
Pediatrics
, vol.61
, pp. 604-610
-
-
Riccardi, V.M.1
Sujansky, E.2
Smith, A.C.3
-
44
-
-
10744226566
-
Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic Syndrome
-
DOI 10.1097/01.ASN.0000113552.59155.72
-
2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome J Am Soc Nephrol 15 722 732 14978175 10.1097/01.ASN. 0000113552.59155.72 (Pubitemid 38294803)
-
(2004)
Journal of the American Society of Nephrology
, vol.15
, Issue.3
, pp. 722-732
-
-
Ruf, R.G.1
Lichtenberger, A.2
Karle, S.M.3
Haas, J.P.4
Anacleto, F.E.5
Schultheiss, M.6
Zalewski, I.7
Imm, A.8
Ruf, E.-M.9
Mucha, B.10
Bagga, A.11
Neuhaus, T.12
Fuchshuber, A.13
Bakkaloglu, A.14
Hildebrandt, F.15
-
45
-
-
3242789449
-
Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome
-
DOI 10.1111/j.1523-1755.2004.00775.x
-
RG Ruf M Schultheiss A Lichtenberger, et al. 2004 Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome Kidney Int 66 564 570 15253707 10.1111/j.1523-1755.2004.00775.x 1:CAS:528:DC%2BD2cXmvVegsL8%3D (Pubitemid 38981996)
-
(2004)
Kidney International
, vol.66
, Issue.2
, pp. 564-570
-
-
Ruf, R.G.1
Schultheiss, M.2
Lichtenberger, A.3
Karle, S.M.4
Zalewski, I.5
Mucha, B.6
Everding, A.S.7
Neuhaus, T.8
Patzer, L.9
Plank, C.10
Haas, J.P.11
Ozaltin, F.12
Imm, A.13
Fuchshuber, A.14
Bakkaloglu, A.15
Hildebrandt, F.16
-
46
-
-
14744273156
-
A role for the Wilms' tumor protein WT1 in organ development
-
H Scholz KM Kirschner 2005 A role for the Wilms' tumor protein WT1 in organ development Physiology 20 54 59 15653840 10.1152/physiol.00048.2004 1:CAS:528:DC%2BD2MXhslKru7k%3D (Pubitemid 40363371)
-
(2005)
Physiology
, Issue.1
, pp. 54-59
-
-
Scholz, H.1
Kirschner, K.M.2
-
47
-
-
7144261709
-
Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations
-
DOI 10.1046/j.1523-1755.1998.00948.x
-
V Schumacher K Schärer E Wühl, et al. 1998 Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations Kidney Int 53 1594 1600 9607189 10.1046/j.1523-1755.1998.00948.x 1:CAS:528:DyaK1cXjs12mu7g%3D (Pubitemid 28243741)
-
(1998)
Kidney International
, vol.53
, Issue.6
, pp. 1594-1600
-
-
Schumacher, V.1
Scharer, K.2
Wuhl, E.3
Altrogge, H.4
Bonzel, K.-E.5
Guschmann, M.6
Neuhaus, T.J.7
Pollastro, R.M.8
Kuwertz-Broking, E.9
Bulla, M.10
Tondera, A.-M.11
Mundel, P.12
Helmchen, U.13
Waldherr, R.14
Weirich, A.15
Royer-Pokora, B.16
-
48
-
-
78249238826
-
Wilms' tumor protein Wt1 regulates the Interleukin-10 (IL-10) gene
-
20974136 10.1016/j.febslet.2010.10.045 1:CAS:528:DC%2BC3cXhsVans7zK
-
LK Sciesielski KM Kirschner H Scholz AB Persson 2010 Wilms' tumor protein Wt1 regulates the Interleukin-10 (IL-10) gene FEBS Lett 584 4665 4671 20974136 10.1016/j.febslet.2010.10.045 1:CAS:528:DC%2BC3cXhsVans7zK
-
(2010)
FEBS Lett
, vol.584
, pp. 4665-4671
-
-
Sciesielski, L.K.1
Kirschner, K.M.2
Scholz, H.3
Persson, A.B.4
-
49
-
-
77956225109
-
Frasier syndrome: Early gonadoblastoma and cyclosporine responsiveness
-
20419325 10.1007/s00467-010-1518-x
-
A Sinha S Sharma A Gulati, et al. 2010 Frasier syndrome: early gonadoblastoma and cyclosporine responsiveness Pediatr Nephrol 25 2171 2174 20419325 10.1007/s00467-010-1518-x
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 2171-2174
-
-
Sinha, A.1
Sharma, S.2
Gulati, A.3
-
50
-
-
0348049699
-
+-exchanger regulatory factor 2 and ezrin
-
DOI 10.1007/s10157-003-0257-8
-
T Takeda 2003 Podocyte cytoskeleton is connected to the integral membrane protein podocalyxin through Na?exchanger regulatory factor 2 and ezrin Clin Exp Nephrol 7 260 269 14712354 10.1007/s10157-003-0257-8 1:CAS:528: DC%2BD2cXlsVCmuw%3D%3D (Pubitemid 38031286)
-
(2003)
Clinical and Experimental Nephrology
, vol.7
, Issue.4
, pp. 260-269
-
-
Takeda, T.1
-
51
-
-
33947367874
-
A proteomic investigation of glomerular podocytes from a Denys-Drash Syndrome patient with a mutation in the Wilms tumour suppressor gene WT1
-
DOI 10.1002/pmic.200600666
-
RL Viney AA Morrison LP van den Heuvel, et al. 2007 A proteomic investigation of glomerular podocytes from a Denys-Drash syndrome patient with a mutation in the Wilms tumour suppressor gene WT1 Proteomics 7 804 815 17295355 10.1002/pmic.200600666 1:CAS:528:DC%2BD2sXjs1KlsLc%3D (Pubitemid 46450657)
-
(2007)
Proteomics
, vol.7
, Issue.5
, pp. 804-815
-
-
Viney, R.L.1
Morrison, A.A.2
Van Den Heuver, L.P.3
Ni, L.4
Mathieson, P.W.5
Saleem, M.A.6
Ladomery, M.R.7
-
53
-
-
79954428312
-
Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations
-
Wasilewska AM, Kuroczycka-Saniutycz E, Zoch-Zwierz W. (2011) Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations. Eur J Pediatr (in press)
-
(2011)
Eur J Pediatr
-
-
Wasilewska, A.M.1
Kuroczycka-Saniutycz, E.2
Zoch-Zwierz, W.3
-
54
-
-
3242795082
-
NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
-
DOI 10.1111/j.1523-1755.2004.00776.x
-
S Weber O Gribouval EL Esquivel, et al. 2004 NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence Kidney Int 66 2 571 579 15253708 10.1111/j.1523-1755. 2004.00776.x 1:CAS:528:DC%2BD2cXmvVegsLw%3D (Pubitemid 38981997)
-
(2004)
Kidney International
, vol.66
, Issue.2
, pp. 571-579
-
-
Weber, S.1
Gribouval, O.2
Esquivel, E.L.3
Moriniere, V.4
Tete, M.-J.5
Legendre, C.6
Niaudet, P.7
Antignac, C.8
|