-
1
-
-
0034100309
-
Changing incidence of glomerular diseases in adults
-
Braden GL, Mulhern JG, O'Shea MH, et al: Changing incidence of glomerular diseases in adults. Am J Kid Dis 2000;35:878.
-
(2000)
Am J Kid Dis
, vol.35
, pp. 878
-
-
Braden, G.L.1
Mulhern, J.G.2
O'Shea, M.H.3
-
2
-
-
0028037335
-
The many masks of focal segmental glomerulosclerosis
-
D'Agati V: The many masks of focal segmental glomerulosclerosis. Kidney Int 1994;46:1223.
-
(1994)
Kidney Int
, vol.46
, pp. 1223
-
-
D'Agati, V.1
-
3
-
-
0036893492
-
Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint
-
Pollak MR: Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint. J Am Soc Nephrol 2002;13:3016-3023.
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 3016-3023
-
-
Pollak, M.R.1
-
4
-
-
0036175951
-
Genetic models: Clues for understanding the pathogenesis of idiopathic nephrotic syndrome
-
Antignac C: Genetic models: Clues for understanding the pathogenesis of idiopathic nephrotic syndrome. J Clin Invest 2002;109:447-449.
-
(2002)
J Clin Invest
, vol.109
, pp. 447-449
-
-
Antignac, C.1
-
6
-
-
0032015551
-
Positionally cloned gene for a novel glomerular protein - Nephrin - Is mutated in congenital nephrotic syndrome
-
Kestila M, Lenkerri U, Mannikko M, et al: Positionally cloned gene for a novel glomerular protein - nephrin - is mutated in congenital nephrotic syndrome. Mol Cell 1988; 1: 575-582.
-
(1988)
Mol Cell
, vol.1
, pp. 575-582
-
-
Kestila, M.1
Lenkerri, U.2
Mannikko, M.3
-
7
-
-
0034034757
-
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
-
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.
-
(2000)
Nat Genet
, vol.24
, pp. 349
-
-
Boute, N.1
Gribouval, O.2
Roselli, S.3
-
8
-
-
0034051681
-
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
-
Kaplan JM, H Kim S, North KN, et al: Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. Nat Genet 2000;24:251.
-
(2000)
Nat Genet
, vol.24
, pp. 251
-
-
Kaplan, J.M.1
Kim, H.S.2
North, K.N.3
-
9
-
-
0033152045
-
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity
-
Winn MP, Conlon PJ, Lynn KL et al: Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity. Genomics 1999;58:113.
-
(1999)
Genomics
, vol.58
, pp. 113
-
-
Winn, M.P.1
Conlon, P.J.2
Lynn, K.L.3
-
10
-
-
1642463951
-
Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin
-
Caridi G, Berdeli A, Dagnino M, Di Duca M, Mir S, Cura A, Ravazzolo R, Ghiggeri GM: Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin. Am J Kidney Dis 2004;43:727-732.
-
(2004)
Am J Kidney Dis
, vol.43
, pp. 727-732
-
-
Caridi, G.1
Berdeli, A.2
Dagnino, M.3
Di Duca, M.4
Mir, S.5
Cura, A.6
Ravazzolo, R.7
Ghiggeri, G.M.8
-
11
-
-
0035199469
-
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis
-
Caridi G, Bertelli R, Carrea A, Di Duca M, Catarsi P, et al: Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis. J Am Soc Nephrol 2001;12:2742-2746.
-
(2001)
J Am Soc Nephrol
, vol.12
, pp. 2742-2746
-
-
Caridi, G.1
Bertelli, R.2
Carrea, A.3
Di Duca, M.4
Catarsi, P.5
-
12
-
-
0036151614
-
Novel mutations in NPHS2 detected in both familial and sporadic steroid resistant nephrotic syndrome
-
Karle SM, Uetz B, Ronner V, Glaeser L, Hildebrandt F, Fuchshuber A, and the Arbeitsgemeinschaft für pädiatrische Nephrologie: Novel mutations in NPHS2 detected in both familial and sporadic steroid resistant nephrotic syndrome. J Am Soc Nephrol 2002;13:388-393.
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 388-393
-
-
Karle, S.M.1
Uetz, B.2
Ronner, V.3
Glaeser, L.4
Hildebrandt, F.5
Fuchshuber, A.6
-
13
-
-
0037407214
-
Broadening the spectrum of disease related to podocin mutations
-
Caridi G, Bertelli R, Di Luca M, et al: Broadening the spectrum of disease related to podocin mutations. J Am Soc Nephrol 2003;14:1278-1286.
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 1278-1286
-
-
Caridi, G.1
Bertelli, R.2
Di Luca, M.3
-
14
-
-
10744226566
-
Patients with mutations in NPHS2 (Podocin) do not respond to standard steroid treatment of nephrotic syndrome
-
Ruf RG, Lichtenberger A, Karle SM, Haas JP, Anacleto FE, Schultheiss M, Zalewski I, Imm A, Ruf EM, Mucha B, Bagga A, Neuhaus T, Fuchshuber A, Bakkaloglu A, Members of the APN Study Group, Hildebrandt F: Patients with mutations in NPHS2 (Podocin) do not respond to standard steroid treatment of nephrotic syndrome. J Am Soc Nephrol 2004;15:722-732.
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 722-732
-
-
Ruf, R.G.1
Lichtenberger, A.2
Karle, S.M.3
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
-
15
-
-
0036897388
-
NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele
-
Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, et al: NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. J Clin Invest 2002;110:1659-1666.
-
(2002)
J Clin Invest
, vol.110
, pp. 1659-1666
-
-
Tsukaguchi, H.1
Sudhakar, A.2
Le, T.C.3
Nguyen, T.4
Yao, J.5
-
16
-
-
0037792031
-
Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood
-
Caridi G, Bertelli R, Scolari F, Sanna-Cherchi S, Di Duca M, Ghiggeri GM: Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood. Kidney Int 2003;64:365.
-
(2003)
Kidney Int
, vol.64
, pp. 365
-
-
Caridi, G.1
Bertelli, R.2
Scolari, F.3
Sanna-Cherchi, S.4
Di Duca, M.5
Ghiggeri, G.M.6
-
17
-
-
0033990048
-
Primer 3 on the www for general users and for biologist programmers
-
Krawetz S, Misener S (eds): Totowa, Humana Press
-
Rozen S, Skaletsky HJ: Primer 3 on the www for general users and for biologist programmers; in Krawetz S, Misener S (eds): Bioinformatics Methods and Protocols: Methods in Molecular Biology. Totowa, Humana Press, 2000, pp 365-386. (Code available at http://www.genome.wi.mit.edu/genome_software/ other/primer3.html.)
-
(2000)
Bioinformatics Methods and Protocols: Methods in Molecular Biology
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.J.2
-
18
-
-
0036158076
-
Not all in the family: Mutations of podocin in sporadic steroid resistant nephrotic syndrome
-
Winn MP: Not all in the family: Mutations of podocin in sporadic steroid resistant nephrotic syndrome. J Am Soc Nephrol 2002;13:577-579.
-
(2002)
J Am Soc Nephrol
, vol.13
, pp. 577-579
-
-
Winn, M.P.1
-
19
-
-
1542318905
-
Podocin and nephrotic syndrome: Implications for the clinician
-
Niaudet P: Podocin and nephrotic syndrome: Implications for the clinician. J Am Soc Nephrol 2004;15:832-834.
-
(2004)
J Am Soc Nephrol
, vol.15
, pp. 832-834
-
-
Niaudet, P.1
-
20
-
-
0037084569
-
Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration
-
Koziell A, Grech V, Hussain S, et al: Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration. Hum Mol Genet 2002;11:379-388.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 379-388
-
-
Koziell, A.1
Grech, V.2
Hussain, S.3
-
21
-
-
1342281104
-
NPHS2 R229Q functional variant is associated with microalbuminuria in the general population
-
Pereira AC, Pereira AB, Mota GF, et al: NPHS2 R229Q functional variant is associated with microalbuminuria in the general population. Kidney Int 2004;65:1026-1030.
-
(2004)
Kidney Int
, vol.65
, pp. 1026-1030
-
-
Pereira, A.C.1
Pereira, A.B.2
Mota, G.F.3
-
22
-
-
0034999807
-
Denaturing high-performance liquid chromatography: A review
-
Xiao W, Oefner PJ: Denaturing high-performance liquid chromatography: A review. Hum Mut 2001;17:439-474.
-
(2001)
Hum Mut
, vol.17
, pp. 439-474
-
-
Xiao, W.1
Oefner, P.J.2
-
23
-
-
12444328765
-
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin
-
Bertelli R, Ginevri F, Caridi G, et al: Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin. Am Kidney Did 2003;41:1314-1321.
-
(2003)
Am Kidney Did
, vol.41
, pp. 1314-1321
-
-
Bertelli, R.1
Ginevri, F.2
Caridi, G.3
-
24
-
-
0036180306
-
Extrarenal effects on the pathogenesis and relapse of idiopathic nephritic syndrome in Buffalo/Mna rats
-
Le Berre L, Godfrin Y, Gunther E, et al: Extrarenal effects on the pathogenesis and relapse of idiopathic nephritic syndrome in Buffalo/Mna rats. J Clin Invest 2002;109:491-498.
-
(2002)
J Clin Invest
, vol.109
, pp. 491-498
-
-
Le Berre, L.1
Godfrin, Y.2
Gunther, E.3
|