-
1
-
-
42149122041
-
Properties of the glomerular barrier and mechanisms of proteinuria
-
Haraldsson B, Nyström J, Deen WM: 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
-
-
77950462459
-
Genetic kidney diseases
-
Hildebrandt F: Genetic kidney diseases. Lancet 375: 1287-1295, 2010
-
(2010)
Lancet
, vol.375
, pp. 1287-1295
-
-
Hildebrandt, F.1
-
3
-
-
77955012444
-
Hereditary nephrotic syndrome: A systematic approach for genetic testing and a review of associated podocyte gene mutations
-
Benoit G, Machuca E, Antignac C: Hereditary nephrotic syndrome: A systematic approach for genetic testing and a review of associated podocyte gene mutations. Pediatr Nephrol 25: 1621-1632, 2010
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 1621-1632
-
-
Benoit, G.1
Machuca, E.2
Antignac, C.3
-
4
-
-
84870546490
-
Circulating suPAR in two cohorts of primary FSGS
-
Wei C, Trachtman H, Li J, Dong C, Friedman AL, Gassman JJ, McMahan JL, Radeva M, Heil KM, Trautmann A, Anarat A, Emre S, Ghiggeri GM, Ozaltin F, Haffner D, Gipson DS, Kaskel F, Fischer DC, Schaefer F, Reiser J; PodoNet and FSGS CT Study Consortia: Circulating suPAR in two cohorts of primary FSGS. J Am Soc Nephrol 23: 2051-2059, 2012
-
(2012)
J am Soc Nephrol
, vol.23
, pp. 2051-2059
-
-
Wei, C.1
Trachtman, H.2
Li, J.3
Dong, C.4
Friedman, A.L.5
Gassman, J.J.6
McMahan, J.L.7
Radeva, M.8
Heil, K.M.9
Trautmann, A.10
Anarat, A.11
Emre, S.12
Ghiggeri, G.M.13
Ozaltin, F.14
Haffner, D.15
Gipson, D.S.16
Kaskel, F.17
Fischer, D.C.18
Schaefer, F.19
Reiser, J.20
more..
-
5
-
-
84866235317
-
Recurrent focal segmental glomerulosclerosis: A discrete clinical entity
-
Torban E, Bitzan M, Goodyer P: Recurrent focal segmental glomerulosclerosis: A discrete clinical entity. Int JNephrol 2012: 246128, 2012
-
(2012)
Int JNephrol
, vol.2012
, pp. 246128
-
-
Torban, E.1
Bitzan, M.2
Goodyer, P.3
-
6
-
-
84873098134
-
Recent progress in the pathophysiology and treatment of FSGS recurrence
-
Cravedi P, Kopp JB, Remuzzi G: Recent progress in the pathophysiology and treatment of FSGS recurrence. Am J Transplant 13: 266-274, 2013
-
(2013)
Am J Transplant
, vol.13
, pp. 266-274
-
-
Cravedi, P.1
Kopp, J.B.2
Remuzzi, G.3
-
7
-
-
33645403170
-
Hereditary proteinuria syndromes and mechanisms of proteinuria
-
Tryggvason K, Patrakka J, Wartiovaara J: Hereditary proteinuria syndromes and mechanisms of proteinuria. N Engl J Med 354: 1387-1401, 2006
-
(2006)
N Engl J Med
, vol.354
, pp. 1387-1401
-
-
Tryggvason, K.1
Patrakka, J.2
Wartiovaara, J.3
-
8
-
-
70349621624
-
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis - A review
-
Löwik MM, Groenen PJ, Levtchenko EN, Monnens LA, van den Heuvel LP: Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis - a review. Eur J Pediatr 168: 1291-1304, 2009
-
(2009)
Eur J Pediatr
, vol.168
, pp. 1291-1304
-
-
Löwik, M.M.1
Groenen, P.J.2
Levtchenko, E.N.3
Monnens, L.A.4
Van Den Heuvel, L.P.5
-
9
-
-
79960510571
-
Genetics of proteinuria: An overview of gene mutations associated with nonsyndromic proteinuric glomerulopathies
-
Piscione TD, Licht C: Genetics of proteinuria: An overview of gene mutations associated with nonsyndromic proteinuric glomerulopathies. Adv Chronic Kidney Dis 18: 273-289, 2011
-
(2011)
Adv Chronic Kidney Dis
, vol.18
, pp. 273-289
-
-
Piscione, T.D.1
Licht, C.2
-
10
-
-
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[R2]: R185-R194, 2009
-
(2009)
Hum Mol Genet
, vol.18
, Issue.R2
, pp. R185-R194
-
-
Machuca, E.1
Benoit, G.2
Antignac, C.3
-
11
-
-
84880573499
-
New developments in steroid-resistant nephrotic syndrome
-
Saleem MA: New developments in steroid-resistant nephrotic syndrome. Pediatr Nephrol 28: 699-709, 2013
-
(2013)
Pediatr Nephrol
, vol.28
, pp. 699-709
-
-
Saleem, M.A.1
-
12
-
-
84876040962
-
Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome
-
McCarthy HJ, Bierzynska A, Wherlock M, Ognjanovic M, Kerecuk L, Hegde S, Feather S, Gilbert RD, Krischock L, Jones C, Sinha MD, Webb NJ, Christian M, Williams MM, Marks S, Koziell A, Welsh GI, Saleem MA; RADAR the UK SRNS Study Group: Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol 8: 637-648, 2013
-
(2013)
Clin J am Soc Nephrol
, vol.8
, pp. 637-648
-
-
McCarthy, H.J.1
Bierzynska, A.2
Wherlock, M.3
Ognjanovic, M.4
Kerecuk, L.5
Hegde, S.6
Feather, S.7
Gilbert, R.D.8
Krischock, L.9
Jones, C.10
Sinha, M.D.11
Webb, N.J.12
Christian, M.13
Williams, M.M.14
Marks, S.15
Koziell, A.16
Welsh, G.I.17
Saleem, M.A.18
-
13
-
-
42149139456
-
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
-
Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE; Molecular Subcommittee of the ACMG Laboratory Quality Assurance Committee: ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007. Genet Med 10: 294-300, 2008
-
(2008)
Genet Med
, vol.10
, pp. 294-300
-
-
Richards, C.S.1
Bale, S.2
Bellissimo, D.B.3
Das, S.4
Grody, W.W.5
Hegde, M.R.6
Lyon, E.7
Ward, B.E.8
-
14
-
-
84885785987
-
Clinical whole-exome sequencing for the diagnosis of mendelian disorders
-
Yang Y, Muzny DM, Reid JG, Bainbridge MN, Willis A, Ward PA, Braxton A, Beuten J, Xia F, Niu Z, Hardison M, Person R, Bekheirnia MR, Leduc MS, Kirby A, Pham P, Scull J, Wang M, Ding Y, Plon SE, Lupski JR, Beaudet AL, Gibbs RA, Eng CM: Clinical whole-exome sequencing for the diagnosis of mendelian disorders. N Engl JMed 369: 1502-1511, 2013
-
(2013)
N Engl JMed
, vol.369
, pp. 1502-1511
-
-
Yang, Y.1
Muzny, D.M.2
Reid, J.G.3
Bainbridge, M.N.4
Willis, A.5
Ward, P.A.6
Braxton, A.7
Beuten, J.8
Xia, F.9
Niu, Z.10
Hardison, M.11
Person, R.12
Bekheirnia, M.R.13
Leduc, M.S.14
Kirby, A.15
Pham, P.16
Scull, J.17
Wang, M.18
Ding, Y.19
Plon, S.E.20
Lupski, J.R.21
Beaudet, A.L.22
Gibbs, R.A.23
Eng, C.M.24
more..
-
15
-
-
84885801095
-
Next-generation sequencing for clinical diagnostics
-
Jacob HJ: Next-generation sequencing for clinical diagnostics. N Engl J Med 369: 1557-1558, 2013
-
(2013)
N Engl J Med
, vol.369
, pp. 1557-1558
-
-
Jacob, H.J.1
-
16
-
-
33645232965
-
Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome
-
Oleggini R, Bertelli R, Di Donato A, Di Duca M, Caridi G, Sanna-Cherchi S, Scolari F, Murer L, Allegri L, Coppo R, Emma F, Camussi G, Perfumo F, Ghiggeri GM: Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome. Gene Expr 13: 59-66, 2006
-
(2006)
Gene Expr
, vol.13
, pp. 59-66
-
-
Oleggini, R.1
Bertelli, R.2
Di Donato, A.3
Di Duca, M.4
Caridi, G.5
Sanna-Cherchi, S.6
Scolari, F.7
Murer, L.8
Allegri, L.9
Coppo, R.10
Emma, F.11
Camussi, G.12
Perfumo, F.13
Ghiggeri, G.M.14
-
17
-
-
0034034757
-
NPHS2, encoding the glomerular protein podocin, ismutated in autosomal recessive steroid-resistant nephrotic syndrome
-
Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C: NPHS2, encoding the glomerular protein podocin, ismutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet 24: 349-354, 2000
-
(2000)
Nat Genet
, vol.24
, pp. 349-354
-
-
Boute, N.1
Gribouval, O.2
Roselli, S.3
Benessy, F.4
Lee, H.5
Fuchshuber, A.6
Dahan, K.7
Gubler, M.C.8
Niaudet, P.9
Antignac, C.10
-
18
-
-
0035199469
-
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis
-
Caridi G, Bertelli R, Carrea A, DiDuca M, Catarsi P, Artero M, Carraro M, Zennaro C, Candiano G, Musante L, Seri M, Ginevri F, Perfumo F, Ghiggeri GM: Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis. J Am Soc Nephrol 12: 2742-2746, 2001
-
(2001)
J am Soc Nephrol
, vol.12
, pp. 2742-2746
-
-
Caridi, G.1
Bertelli, R.2
Carrea, A.3
DiDuca, M.4
Catarsi, P.5
Artero, M.6
Carraro, M.7
Zennaro, C.8
Candiano, G.9
Musante, L.10
Seri, M.11
Ginevri, F.12
Perfumo, F.13
Ghiggeri, G.M.14
-
19
-
-
36048978116
-
NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome
-
Berdeli A, Mir S, Yavascan O, Serdaroglu E, Bak M, Aksu N, Oner A, Anarat A, Donmez O, Yildiz N, Sever L, Tabel Y, Dusunsel R, Sonmez F, Cakar N: NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome. Pediatr Nephrol 22: 2031-2040, 2007
-
(2007)
Pediatr Nephrol
, vol.22
, pp. 2031-2040
-
-
Berdeli, A.1
Mir, S.2
Yavascan, O.3
Serdaroglu, E.4
Bak, M.5
Aksu, N.6
Oner, A.7
Anarat, A.8
Donmez, O.9
Yildiz, N.10
Sever, L.11
Tabel, Y.12
Dusunsel, R.13
Sonmez, F.14
Cakar, N.15
-
20
-
-
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, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB, Pereira AB, Kalluri R, Pollak MR: NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. J Clin Invest 110: 1659-1666, 2002
-
(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
Schwimmer, J.A.6
Schachter, A.D.7
Poch, E.8
Abreu, P.F.9
Appel, G.B.10
Pereira, A.B.11
Kalluri, R.12
Pollak, M.R.13
-
21
-
-
33748709227
-
Expression profile of nephrin, podocin, and CD2AP in Chinese children with MCNS and IgA nephropathy
-
Mao J, Zhang Y, Du L, Dai Y, Yang C, Liang L: Expression profile of nephrin, podocin, and CD2AP in Chinese children with MCNS and IgA nephropathy. Pediatr Nephrol 21: 1666-1675, 2006
-
(2006)
Pediatr Nephrol
, vol.21
, pp. 1666-1675
-
-
Mao, J.1
Zhang, Y.2
Du, L.3
Dai, Y.4
Yang, C.5
Liang, L.6
-
22
-
-
0037338559
-
Nail patella syndrome: A review of the phenotype aided by developmental biology
-
Sweeney E, Fryer A, Mountford R, Green A, McIntosh I: Nail patella syndrome: A review of the phenotype aided by developmental biology. J Med Genet 40: 153-162, 2003
-
(2003)
J Med Genet
, vol.40
, pp. 153-162
-
-
Sweeney, E.1
Fryer, A.2
Mountford, R.3
Green, A.4
McIntosh, I.5
-
23
-
-
79952198057
-
Exome sequencing: The sweet spot before whole genomes
-
Teer JK, Mullikin JC: Exome sequencing: The sweet spot before whole genomes. Hum Mol Genet 19[R2]: R145-R151, 2010
-
(2010)
Hum Mol Genet
, vol.19
, Issue.R2
, pp. R145-R151
-
-
Teer, J.K.1
Mullikin, J.C.2
-
24
-
-
33646406847
-
Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin
-
Huber TB, Kwoh C, Wu H, Asanuma K, Gödel M, Hartleben B, Blumer KJ, Miner JH, Mundel P, Shaw AS: 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
Kwoh, C.2
Wu, H.3
Asanuma, K.4
Gödel, M.5
Hartleben, B.6
Blumer, K.J.7
Miner, J.H.8
Mundel, P.9
Shaw, A.S.10
-
25
-
-
84900028974
-
Nephrotic syndrome in children: From bench to treatment
-
Davin JC, Rutjes NW: Nephrotic syndrome in children: From bench to treatment. Int J Nephrol 2011: 372304, 2011
-
(2011)
Int J Nephrol
, vol.2011
, pp. 372304
-
-
Davin, J.C.1
Rutjes, N.W.2
-
26
-
-
77950212549
-
The spectrum of FSGS: Does pathologymatter?
-
Fogo AB: The spectrumof FSGS: Does pathologymatter? Nephrol Dial Transplant 25: 1034-1036, 2010
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 1034-1036
-
-
Fogo, A.B.1
-
27
-
-
84929072114
-
Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis
-
published online ahead of print April 21, 2014
-
Laurin LP, Lu M, Mottl AK, Blyth ER, Poulton CJ, Weck KE: Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis [published online ahead of print April 21, 2014]. Nephrol Dial Transplant
-
Nephrol Dial Transplant
-
-
Laurin, L.P.1
Lu, M.2
Mottl, A.K.3
Blyth, E.R.4
Poulton, C.J.5
Weck, K.E.6
-
28
-
-
70149084338
-
Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation
-
Malina M, Cinek O, Janda J, Seeman T: Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation. Pediatr Nephrol 24: 2051-2053, 2009
-
(2009)
Pediatr Nephrol
, vol.24
, pp. 2051-2053
-
-
Malina, M.1
Cinek, O.2
Janda, J.3
Seeman, T.4
-
29
-
-
33751531864
-
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
-
Hinkes B, Wiggins RC, Gbadegesin R, Vlangos CN, Seelow D, Nürnberg G, Garg P, Verma R, Chaib H, Hoskins BE, Ashraf S, Becker C, Hennies HC, Goyal M, Wharram BL, Schachter AD, Mudumana S, Drummond I, Kerjaschki D, Waldherr R, Dietrich A, Ozaltin F, Bakkaloglu A, Cleper R, Basel-Vanagaite L, Pohl M, Griebel M, Tsygin AN, Soylu A, Müller D, Sorli CS, Bunney TD, Katan M, Liu J, Attanasio M, O 'toole JF, Hasselbacher K, Mucha B, Otto EA, Airik R, Kispert A, Kelley GG, Smrcka AV, Gudermann T, Holzman LB, Nürnberg P, Hildebrandt F: 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
Wiggins, R.C.2
Gbadegesin, R.3
Vlangos, C.N.4
Seelow, D.5
Nürnberg, 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
Müller, 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
Nürnberg, P.46
Hildebrandt, F.47
more..
-
30
-
-
47749155993
-
Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome-a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische Nephrologie
-
Plank C, Kalb V, Hinkes B, Hildebrandt F, Gefeller O, Rascher W; Arbeitsgemeinschaft für Pädiatrische Nephrologie: Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome-a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische Nephrologie. Pediatr Nephrol 23: 1483-1493, 2008
-
(2008)
Pediatr Nephrol
, vol.23
, pp. 1483-1493
-
-
Plank, C.1
Kalb, V.2
Hinkes, B.3
Hildebrandt, F.4
Gefeller, O.5
Rascher, W.6
-
31
-
-
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, Hildebrandt F; Arbeitsgemeinschaft Für Pädiatrische Nephrologie Study Group: Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. J Am Soc Nephrol 15: 722-732, 2004
-
(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
-
32
-
-
77954534482
-
Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations
-
Gellermann J, Stefanidis CJ, Mitsioni A, Querfeld U: Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations. Pediatr Nephrol 25: 1285-1289, 2010
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 1285-1289
-
-
Gellermann, J.1
Stefanidis, C.J.2
Mitsioni, A.3
Querfeld, U.4
-
33
-
-
78149355246
-
Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome
-
Büscher AK, Kranz B, Büscher R, Hildebrandt F, Dworniczak B, Pennekamp P, Kuwertz-Bröking E, Wingen AM, John U, Kemper M, Monnens L, Hoyer PF, Weber S, Konrad M: Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol 5: 2075-2084, 2010
-
(2010)
Clin J am Soc Nephrol
, vol.5
, pp. 2075-2084
-
-
Büscher, A.K.1
Kranz, B.2
Büscher, R.3
Hildebrandt, F.4
Dworniczak, B.5
Pennekamp, P.6
Kuwertz-Bröking, E.7
Wingen, A.M.8
John, U.9
Kemper, M.10
Monnens, L.11
Hoyer, P.F.12
Weber, S.13
Konrad, M.14
-
34
-
-
84863442222
-
KDIGO Clinical Practice Guideline for Glomerulonephritis
-
Kidney Disease: Improving Global Outcomes (KDIGO) Glomerulonephritis Work Group. KDIGO Clinical Practice Guideline for Glomerulonephritis. Kidney Int Suppl 2: S139-S174, 2012
-
(2012)
Kidney Int Suppl
, vol.2
, pp. S139-S174
-
-
-
35
-
-
78651393550
-
Carrier testing for severe childhood recessive diseases by next-generation sequencing
-
Bell CJ, Dinwiddie DL, Miller NA, Hateley SL, Ganusova EE, Mudge J, Langley RJ, Zhang L, Lee CC, Schilkey FD, Sheth V, Woodward JE, Peckham HE, Schroth GP, Kim RW, Kingsmore SF: Carrier testing for severe childhood recessive diseases by next-generation sequencing. Sci Transl Med 3: ra4, 2011
-
(2011)
Sci Transl Med
, vol.3
, pp. ra4
-
-
Bell, C.J.1
Dinwiddie, D.L.2
Miller, N.A.3
Hateley, S.L.4
Ganusova, E.E.5
Mudge, J.6
Langley, R.J.7
Zhang, L.8
Lee, C.C.9
Schilkey, F.D.10
Sheth, V.11
Woodward, J.E.12
Peckham, H.E.13
Schroth, G.P.14
Kim, R.W.15
Kingsmore, S.F.16
-
36
-
-
84864365555
-
Characterization of renal progenitors committed toward tubular lineage and their regenerative potential in renal tubular injury
-
Angelotti ML, Ronconi E, Ballerini L, Peir0ed A, Mazzinghi B, Sagrinati C, Parente E, Gacci M, Carini M, Rotondi M, Fogo AB, Lazzeri E, Lasagni L, Romagnani P: Characterization of renal progenitors committed toward tubular lineage and their regenerative potential in renal tubular injury. Stem Cells 30: 1714-1725, 2012
-
(2012)
Stem Cells
, vol.30
, pp. 1714-1725
-
-
Angelotti, M.L.1
Ronconi, E.2
Ballerini, L.3
Peiroed, A.4
Mazzinghi, B.5
Sagrinati, C.6
Parente, E.7
Gacci, M.8
Carini, M.9
Rotondi, M.10
Fogo, A.B.11
Lazzeri, E.12
Lasagni, L.13
Romagnani, P.14
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